online medical research courses

9 Best + Free Medical Research Courses [Harvard | Stanford | Yale] [2024 October]

Medical research is the bedrock upon which advancements in healthcare and medicine are built. It is through rigorous research that groundbreaking discoveries are made, innovative treatments are developed, and deeper insights into complex diseases are gathered. Medical research encompasses a vast domain, from clinical trials and biomedical studies to epidemiological analyses and molecular investigations. The knowledge and methodologies applied in this domain have the potential to shape healthcare policies, inform medical practices, and, most crucially, save and enhance lives. With the ever-accelerating pace of medical advancements and the increasing complexities of global health challenges, there’s a growing need for skilled professionals who can navigate the multifaceted world of medical research.

To cater to the burgeoning demand for expertise in this field, numerous online courses have been curated and designed to provide in-depth knowledge and practical skills in various aspects of medical research. However, amidst the overwhelming number of courses available, pinpointing those that offer comprehensive, cutting-edge, and authentic knowledge can be an endeavor. This is where DigitalDefynd comes to the fore. With an unwavering commitment to elevating the standards of online education, we’ve reviewed numerous courses to curate a list of the Best and Free Medical Research Courses . Created and led by leading experts and researchers, each course on our list promises an enriching and holistic learning experience.

Whether you’re a medical professional, a budding researcher, or someone with a keen interest in the intricacies of medical science, our curated selection offers a pathway to deep understanding and mastery. Delve into these courses and set forth on a path that holds the potential to redefine the landscape of healthcare and medicine. Have a look at our Best Healthcare Courses.

9 Best + Free Medical Research Courses & Classes [2024 October]

Free course trial – understanding medical research by yale university (coursera).

Developed by F. Perry Wilson, this is an excellent course on medical research that will provide you with the tools and skills that you need to interpret medical studies critically and determine the difference between good and bad science . During the course, you will cover study designs, research methods, and statistical interpretation, as well as you will learn about the dark side of the medical research while covering fraud, biases, and common misinterpretations of data. Moreover, the course provides you with multiple video lectures and downloadable resources to improve your overall learning process. Also, after successful completion, you will get a certificate of completion signed by Yale University faculty.

Highlights –

– Learn how to read a medical research paper efficiently while differentiating between good and bad science on your own.

– Know about the various tests used in medical research and how to spot common errors in methodology and inter-operation for each.

– Be able to read and analyze statistical figures, charts, and graphics, and verify the claims made in news articles.

– Gain knowledge and access to the tools that you need to determine the trustworthiness of the scientific information that you read.

– Get continuous support from an expert community who will help and advice you on understanding medical research.

Duration: 16 hours

Rating: 4.9 out of 5

You can Sign up Here

Free Course Trials – Clinical Research Courses (Coursera)

If you’re not getting the best clinical research courses available on e-learning platforms, then this list of courses offered by Coursera might help you in your quest. Coursera offers multiple clinical research courses that are provided by top universities around the world, such as Johns Hopkins University, Stanford University, University of California San Diego, and many more. Among these courses, some of the best courses that you should enroll-in include Introduction to Systematic Review and Meta-Analysis, Understanding Clinical Research: Behind the Statistics , Clinical Epidemiology, Fundamentals of Immunology, etc. Also, each course is included with guided projects that you will need to submit at the end of the course to obtain your certificate of completion. Don’t forget to check our list of Best Healthcare Management Courses .

– A list of practical and knowledgeable courses created by some of the best universities around the world to help individuals learn about clinical and medical research.

– Learn about design and interpretation of clinical trials, data management of clinical research, drug development, and biostatistics in public health.

– Learn how to do clinical research with Wolfram language while getting an introduction to the biology of cancer and the data science of health informatics.

– Access various downloadable resources, workbooks, quizzes, graded assignments, and hands-on projects with every course.

Duration: Self-paced

Rating: 4.4 out of 5

Free Course Trial – Understanding Clinical Research: Behind the Statistics by University of Cape Town (Coursera)

Whether you are a clinical practitioner who reads research articles to stay up-to-date with developments or a medical student who wants to learn how to approach your own research paper, then this course is the best choice for you. Taking up this course with full attention will provide you the confidence that you need to understand statistical analysis, published literature, and conducting your own research . The course is developed by Juan H Klopper, who is a professional instructor at the University of Cape Town. During the course, he will assist you personally via live video sessions of emails to provide you an improved understanding of the course material.

– A practical course that gives you an easy entry into interpreting common statistical concepts without getting into nitty-gritty mathematical formulae.

– Get an intuitive understanding of clinical research results with a practical orientation to the field of medical research and commonly used statistical analysis.

– Build an intuitive understanding of statistical analysis with the concept of a p-value, and then move on to the probability theory, the central limit theorem, and data distribution.

– Absolutely free to enroll without any hidden charges and the freedom to study from the comfort of your home.

Duration: 5-6 weeks, 4-5 hours/week

Rating: 4.8 out of 5

Related: How Can Healthcare Leaders Use AI?

Free Course Trial – Data Management for Clinical Research by Vanderbilt University (Coursera)

This introductory course will familiarize you with the critical concepts and practical methods of supporting planning, collecting, storing, and disseminating data in clinical research . Taking this course will help you learn and understand why implementing solid data management principles are critical for any scientific domain. The course is developed by professional instructors of Vanderbilt University, who are well-versed with all the concepts of clinical research. They will provide you additional assistance during the course to help you gain a better understanding of the clinical research. Also, after concluding the course, you will earn your certificate of completion that can be shared with employers to showcase your skills.

– Learn the fundamental concepts of clinical research while discussing the best practices for designing clinical research data collection.

– Cover the standards of study processes, ideas for regulatory compliance, and electronic data capture fundamentals.

– Get a walkthrough into various concepts of clinical research, such as creating visit forms, copying variables, renaming forms, testing the REDCap project, etc.

– Included with practical lessons, short quizzes with each session, graded assignments, and hands-on exercises with best practices for data management.

– Get continuous support and help from a team of experts to resolve your problems related to the course.

Duration: 18 hours

Rating: 4.7 out of 5

Healthcare Analytics: AI, Big Data & Digital Transformations (Rotman School of Management)

Offered by Rotman School of Management, this online healthcare analytics program will enable you to learn how to ask the right questions to data analysts while building data analytics knowledge. Enrolling in this productive prospectus will allow you to learn how to use data to drive cultural change in your organization . The curriculum is prepared with a step-by-step approach to help you gain comprehensive knowledge of the significance of the emerging roles of artificial intelligence in healthcare and its applications for improving your organizational processes and outcomes. At the end of the curriculum, you’ll get to work with real-world application exercises, knowledge checks, and various quizzes.

– A blended syllabus to learn how to craft the narrative for your organization’s data literacy while improving the data fluency

– Learn to explore the data generation process, how to categorize data, the different types of variables used with data, and analysis for the healthcare industry

– Learn to examine the impact of data distribution and the purpose of dashboards in monitoring key performance indicators

– Know about effective strategies for applying regression analysis to make predictions and estimate the effect and the knowledge

Duration: 7 weeks, 4-6 hours/week

Rating: 4.5 out of 5

Online Medical Research Courses (Harvard University)

Whether you’re just beginning with clinical research or already have hands-on experience in it, this list of courses can help you improve your knowledge in every manner. There are three different courses available on the platform, which are designed by the best instructors of Harvard University, who have been teaching multiple students for years . Completing these courses will acknowledge you about almost everything that you need to understand research papers and write your own research paper. Also, you will get the opportunity to join a student support community, where you can interact with other students and instructors to submit your queries and resolutions.

– Learn about prescription drug regulations, costs, and access while understanding how the FDA regulates pharmaceuticals.

– Know the process of discovering, testing, and approving innovative drugs, as well as cover the perspectives on the criteria used for drug approval.

– Gain an inside look at tumor sequencing approaches and analysis and understand the links between genetics and cancer.

– Understand the basics of tumor immunology and how advanced knowledge of the immune system can impact patient care.

– Get access to recorded video sessions, graded assignments, hands-on exercises, practical exams, and much more to improve your overall learning.

Rating: 4.6 out of 5

Related: Application of Data Science in Healthcare and Medicine for Improved Patient Outcomes

Online Clinical Research Certificate Program (Drexel University)

Delivered by industry experts and professional instructors of Drexel University, this online clinical research program is specifically designed for individuals who are seeking clinical research credentials and want to make a successful career in the clinical research field . It is a 15-semester credit program, during which you will cover both business principles and clinical research industry best practices. Also, you will have to complete five graduate-level courses that contain information from the MS in Clinical Research Organization and Management curriculum to earn your professional credential from Drexel University. While learning from the sessions, if you face any problems or queries, then a team of experts will always be available to help you. Check out our take on Best Health Informatics Courses. 

– A professional certification program that will prepare you for the role of clinical research associate, analyst, or clinical research coordinator.

– Learn how to keep up with the changes in clinical research, financial, legal, and regulatory environments while gaining an in-depth understanding of the fundamentals of compliance, clinical trials, and pharmaceutical laws.

– Be able to build skills that are relevant to you and can help you navigate the evolving clinical research landscapes successfully.

– Tailor your study plan according to your requirements with the comfort of studying from your home.

Improving Healthcare through Clinical Research by the University of Leeds (FutureLearn)

This is a free online course that can help you find out how medical treatments are developed, tested, and appraised to improve healthcare for all. The course is developed by professional instructors of Leeds University, who are experienced in all aspects of clinical research. During the course, the instructors will take you through various case studies to examine how research contributes to the treatment of major diseases like cancer and dementia . Accredited by Certification Service, it will provide you with a certificate of completion after finishing the course with given assignments.

– A valuable course that focuses on the process of discovery, how it is used to improve healthcare, and the important ethical questions raised by research.

– Learn the fundamental concepts of the scientific process, and their importance in ensuring that clinical research delivers accurate information and answers.

– Understand how modern clinical trials are conducted, the importance of minimizing bias, and the role of techniques like placebos, blinding, randomization, and control.

– Know the importance of ensuring that clinical research is ethical and the fundamental values that are vital to ensure that clinical trials are set up and conducted in an ethically sound manner.

Duration: 4 weeks, 4-5 hours/week

Thinking Critically: Interpreting Randomized Clinical Trials by Stanford Online (edX)

Developed by experienced instructors of Stanford University, this course can fulfill the clinical community’s need to improve your skills in the critical evaluation of clinical research papers. Enrolling in this course will help you learn how having essential skills of the appraisal can have a significant impact by improving quality of research projects, clinical practice, and peer-review of manuscripts and grants . Besides, it is included with recorded video lectures, practical assessments, grading quizzes with each session, and downloadable resources to provide you additional knowledge of critical research concepts. After ending this course, you will gain a certificate of completion signed by Stanford University.

– A knowledgeable course that will improve your thinking capability regarding clinical research and creating your own research papers.

– Included with efficient and engaging videos with relevant clinical examples to cover essential research methodology principles.

– Learn how to analyze the concepts of randomization and blinding to reduce bias, as well as how to develop strategies to critically appraise randomized clinical trials and determine whether the study results are valid or not.

– Offer opportunities like self-paced learning and practicing critical appraisal of a variety of published studies that evaluate benefit, harm, and prognosis.

Duration: 1 week

Rating: 4.3 out of 5

Related: Reasons to learn Bioinformatics

Bonus: Free Medical Research Courses

Free course – good clinical practice – ich guidelines e6 r2 (alison).

Alison’s “Good Clinical Practice – ICH Guidelines E6 R2” course provides an authoritative guide to the international standards for conducting clinical trials involving human subjects. This course includes the ethical and scientific standards of quality to guarantee the protection of trial participants’ rights, safety, and well-being and the credibility of clinical trial data. Learners will delve into the responsibilities of investigators, sponsors, and ethics committees, as well as detailed protocols for audit trails, informed consent forms, and safety reports. The course aims to equip researchers, clinical coordinators, and healthcare professionals with the necessary knowledge to uphold the integrity and compliance of clinical research.

Duration:  3-4 hours

Free Course –  Master Clinical Research Comprehensive Basic Guide (Udemy)

Udemy’s “Master Clinical Research Comprehensive Basic Guide” offers a quick yet thorough introduction to the essentials of clinical research. This course is designed for those new to the field or looking to solidify their understanding of core concepts. It addresses the basic principles of designing and conducting clinical studies, including understanding different study designs, ethical considerations’ significance, and data collection and analysis basics. This course is perfect for students, new researchers, and healthcare professionals, as it offers a strong base for those getting ready to participate in or supervise clinical research projects.

Duration: 51 minutes

Free Course –  Research Skills for Healthcare (Alison)

Alison’s “Research Skills for Healthcare” course is aimed at healthcare professionals and students interested in improving their research skills within the healthcare sector. This comprehensive course covers various topics crucial for conducting high-quality medical research, including literature review strategies, research design, ethical considerations, and statistical analysis. It provides practical guidance on conducting research that can lead to evidence-based practice, essential for patient care and healthcare policy. Additionally, the course delves into the complexities of data interpretation and how to communicate research findings to both scientific and non-scientific audiences effectively. By equipping healthcare professionals with these critical research skills, the course enables them to contribute to advancing healthcare practices and interventions.

Duration: 1.5-3 hours

Free Course –  Scientific Method in Research Methodology (Udemy)

Udemy’s “Scientific Method in Research Methodology” course provides a focused exploration into the foundational principles that govern the scientific method in research. This course is particularly designed for those new to scientific research or those seeking to solidify their understanding of how rigorous research is conducted. It breaks down the steps of the scientific method, from hypothesis formulation and variable identification to data collection and analysis. The course strongly focuses on the significance of critical thinking and ethical aspects in research. It instructs participants on assessing and understanding findings with honesty and precision. By covering these essential aspects, the course prepares learners to apply the scientific method effectively in their respective fields, enhancing the quality and reliability of their research outcomes.

Duration: 35 minutes

Free Course –  Essentials of Clinical Research (Alison)

Alison’s course “Essentials of Clinical Research” provides a priceless source of knowledge for individuals seeking to enhance their comprehension of the methodologies and operational factors involved in clinical studies. This course addresses the fundamental aspects of clinical research, including the design of clinical trials, the regulatory environment, and the ethical obligations to participants. It thoroughly explores the process of developing and managing clinical trials, emphasizing the importance of adhering to international standards and regulatory requirements. The course also teaches about data management, the importance of maintaining patient confidentiality, and the steps required to ensure the accuracy and reliability of trial results. By equipping learners with these essential skills, the course prepares them for careers in clinical research, enhancing their ability to contribute to advancements in medical science and patient care.

Duration:  1.5-3 hours

So these were the 8 Best Medical Research Courses, Classes, Tutorials, Training and Certification program available online for. DigitalDefynd’s Medical Research Courses offer a rigorous and insightful learning experience for individuals eager to contribute to the advancement of medical science. These courses provide the essential skills, knowledge, and methodologies necessary to conduct robust medical research, analyze complex data, and interpret results accurately. Embrace the opportunity to enhance your research capabilities and make meaningful contributions to the field of medicine. Start your journey with DigitalDefynd today and unlock your potential to drive innovation and improve healthcare outcomes through cutting-edge medical research.

We wish you Happy Learning! 🙂

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Clinical Research Certification

Clinical research training.

Get Clinical Research Certification with Comprehensive Clinical Trials Training Online

Get clinical research career training in 1 to 4 weeks with our online accredited clinical research courses. Trusted by organizations and experienced researchers.

Advanced ICH GCP Certification (AGCPC)

Objectives: Provide an advanced and engaging review of International Conference on Harmonization Good Clinical Practice (ICH GCP) guidelines updated for 2024.

Students Enrolled: 3,166†

Students came from: Multiple universities, hospitals, research facilities, contract research organizations, medical practices, and biopharmaceutical companies at different stages

Requirements: HS Diploma or GED

Format: Advanced, online, self-paced.

Length: 16 Hours. Online, self paced, start anytime.

Accreditation: ACCRE, Transcelerate Biopharma

Certification: Clinical research certificate online. Exam score 70% or higher on 2 attempts.

Graduates work at: University research groups, hospitals, clinics, clinical trial sites, pharmaceutical companies, and government agencies

Graduate Job Roles after course: ICH GCP clinical research training is required every 2 years for all research roles thus our graduates work in a range of fields.

Research roles: Research Assistant, Lab Assistant, Research Coordinator, Research Scholar, Postdoctoral Researcher, Graduate Research Assistant, etc. Intern roles: Research Assistant Intern, Outpatient Pharmacy Intern, Clinical roles: Clinical Affairs Intern, Clinical Fellow, Clinical Nurse, Clinical Operations Manager, Clinical Research Professional Teaching roles: Assistant Professor, Lecturer, Graduate Teaching Assistant, etc. Management roles: Clinical Research Manager, Pharmacy Operations Manager, Associate Director of Clinical Development, Vice President of Clinical Development Specialized roles: Drug Safety Associate, Regulatory Specialist, Scientific Consultant, Medical Laboratory Scientist, Pharmacovigilance Associate Other roles: NHS Primary Care QI Facilitator, Government Healthcare Recruiter, Research Ethics Coordinator (based on review of new job positions after enrollment in course)

Pharmacovigilance and Drug Safety

Advanced Pharmacovigilance and Argus Safety Certification (APVASC)

Objectives: Gain advanced education in pharmacovigilance management and proficiency in international regulatory affairs and drug safety monitoring.

Students Enrolled: 5,708†

Students came from: CROs, pharmacies, pharmaceutical companies,

Requirements: Bachelors in Biology or Natural Science OR Pharmacist Degree. Many roles require prior clinical research experience which can be gained by other entry level positions through our CRC or ICH GCP clinical research training certification.

Length: 110 Hours. Online clinical research course, self paced, start anytime.

Accreditation: ACCRE, Joint Accreditation for CE with ACPE 17.5 CME for Pharmacists.

Certification: Online certificate. Exam score 70% or higher on 2 attempts.

Graduates work at: Pharmaceutical and Biotech Companies, Healthcare Service Providers, Regulatory Bodies and Research Institutes, Consulting and Services Companies, Consumer Goods Companies, Healthcare Information and Service.

Graduate Hired As: Regulatory Affairs Associate, Clinical Trial Drug Safety Associate, Drug Safety Specialist, Patient Safety Senior Associate, Pharmacovigilance Scientist, Pharmacovigilance Manager, Senior Pharmacovigilance Associate, Pharmacovigilance Regional Head, Pharmacovigilance Analyst, Senior Director Quality, Pharmacovigilance Data Entry Manager, Principal Pharmacovigilance Scientist, QA & Medical Complaint Handling Associate, Senior Manager Medical Safety Officer, Medical Affairs Senior Scientist, Quality Manager, VP Medical Affairs, Clinical Guidelines Coordinator, Clinical Data Monitor, Pharmacovigilance Specialist, Regulatory Project Manager, Product Safety Manager, Manager Pharmacovigilance Operations, Regulatory Affairs Manager, Clinical Pharmacist Consultant, Product Vigilance Manager, Epidemiologist, Senior Manager Safety and Pharmacovigilance, Associate Director of Pharmacovigilance Department, Qualified Person Responsible for Pharmacovigilance (QPPV), Pharmacovigilance Deputy, Regulatory Affairs Manager, Senior Scientist, Senior Medical Advisor, Cosmetovigilance, Drug Safety and Medical Information Specialist, Environmental Analyst, Vice President Clinical Development, Operation Specialist (Life Cycle Safety/Drug Safety/Medical Information), Regulatory Affairs Supervisor & QPPV, Senior Director Clinical Operations, Safety, and Customer Service Excellence, Regulatory Affairs - Pharmacist, Vice President Operations, QA Executive, Health Advisor Pharmacist, COVID Health Specialist - Case and Contact Manager, Senior Project Manager, Pharmacy Manager, R&D Post-Implementation Service, Pharmacy Manager, Investigations Associate, Lead Clinical Operations Safety/Quality Responsible, Pharmacist, Trial and Supply Management, etc. (based on review of new job positions post-enrollment)

Clinical Research Associate

Advanced clinical research associate certification (acrac).

Objective: Obtain a thorough understanding of clinical research to proficiently fulfill the duties of a Clinical Research Associate.

Students Enrolled: 7,536†

Students came from: Pharmaceuticals and Biotech Companies, Clinical Research and Consulting Services, Hospitals and Healthcare Providers, Universities and Academic Institutions

Requirements: Seeking candidates with a Bachelor's in Biology/Natural Science, Nursing Degree, or MBBS/IMG Degree for entry-level positions . Consider obtaining ACRP or SOCRA credentials after gaining 2 years of experience. Students with credentials and/or 2 years of experience (18% of cohort) still choose our course to refresh their knowledge because of our comprehensive review.

Length: 200 Hours. Online, self paced, start anytime.

Accreditation: ACCRE, Joint Accreditation for CE with ACCME, ANCC, ACPE, ICPE for 17.5 CME for Physicians, Nurses, Pharmacists, and Healthcare Professionals. Candidate for Federally Qualified Post-Graduate Institution with MSA-CESS.

Graduates work at: Pharmaceutical and Biotech Companies, Clinical Research and Consulting Services, Consulting and Professional Services, Consumer Goods Companies, Hospitals and Healthcare Providers, Government Health Departments, Universities and Academic Institutions, Healthcare IT and Services.

Graduate job roles post-course: Clinical Research Associate, Clinical Trial Monitor II, Research Associate, CRA II, Scientist, Quality Assurance Analyst, Senior Clinical Research Associate, Research Associate in Discovery Immunology, Clinical Trial Monitor/CRA, Clinical Trials Project Manager, Associate Director of Research Nursing, Clinical Trial Navigator, Clinical Director for R&D, Senior Clinical Research Associate, Clinical Research Professional, Medical Science Liaison, Clinical Trial Associate III, Quality Assurance Associate II, IRB/SRC Analyst II, Project Manager, Clinical Trial Associate, Clinical Research Coordinator, Public Health Advisor, Associate Scientist II, Strategy Analyst, Clinical Research Associate II, Clinical Operations Specialist, Advisor - Development Clinical Research Scientist, Neuroscience, Associate Clinical Engineer, Clinical Trial Management Associate, Quality Supervisor, Clinical Research Data Coordinator (based on review of new job positions post-enrollment)

Clinical Research Coordinator

Advanced clinical research coordinator certification (acrcc).

Objective: Acquire comprehensive proficiency in clinical research coordinator training encompassing patient care, regulatory compliance, and trial oversight.

Students Enrolled: 3,653†

Students came from: Hospitals and Healthcare Providers:, Clinical Research and Consulting Services, Healthcare Services, Pharmaceutical and Biotech Companies, Clinical Research Centers

Requirements: HS Diploma or GED OR Nurses OR Professionals with patient experience.

Length: 150 Hours. Online, self paced, start anytime.

Accreditation: ACCRE, Joint Accreditation with ANCC for 17.5 CME for nurses.

Graduates work at: Pharmaceutical and Biotech Companies, Hospitals and Healthcare Providers, Universities and Academic Institutions, Clinical Research and Consulting Services, Diagnostic Services, Consumer Goods Companies, Healthcare Services, Cancer Treatment and Research Centers.

Graduate job roles post-course: Clinical Research Coordinator, Clinical Research Coordinator II, Lead Clinical Research Coordinator, Senior Clinical Research Coordinator, Oncology Research Coordinator, Clinical Study Coordinator, Clinical Research Data Coordinator, Clinical Research Nurse, Clinical Director/ Office Manager, Regulatory Contact/ Clinical Research Coordinator, Clinical Research/Regulatory Coordinator, Clinical Trials Specialist, Research Regulatory Specialist, Certified Clinical Research Coordinator, Clinical Research Specialist, Sr. Director of Clinical Operations   (based on review of new job positions post-enrollment)

Clinical Research Assistant

Advanced Clinical Trial Assistant Certification (ACTAC)

Objective: Enhance skills required to support clinical trials, focusing on trial conduct, data collection, and administrative duties.

Students Enrolled: 1,800†

Students came from: Various universities, hospitals, clinics, and clinical research sites, etc.

Requirements: HS Diploma or GED. Current high-schoolers with evidence of active research internship can enroll.

Length: 50 Hours. Online, self paced, start anytime.

Accreditation: ACCRE, Transcelerate Biopharma.

Graduates work at: Various universities, hospitals, clinics, scholarships, internships, and clinical research sites.

Graduate job roles post-course: Clinical research assistant, clinical trial assistant, clinical researcher professional, clinical research coordinator, trial assistant, research assistant.

Clinical Research Project Manager

Advanced Clinical Research Project Manager Certification (ACRCC)

Objective: Prepare students for clinical research management certificate by teaching them how to effectively oversee large-scale clinical studies, ensuring adherence to protocols, budget, and timelines.

Students Enrolled: 1,190†

Students came from: Several CROs, universities, hospitals, clinics.

Requirements: Prior Project Management or Clinical Research Experience.

Accreditation: ACCRE, Joint Accreditation for CME

Certification: Online certificate. Exam score 70% or higher on 2 attempts. 

Graduates work at: Pharmaceutical and Biotech Companies, Clinical Research and Consulting Services, Healthcare Staffing, Universities and Academic Institutions

Physician Medical Monitor

Advanced physician medical monitor certification (apmmc).

Prepare physicians for the specialized role of Medical Monitor, with an emphasis on patient safety, protocol adherence, and data interpretation.

Students Enrolled: 1,438†

Requirements: Medical Degree (MBBS, IMG, FMG).

Accreditation: ACCRE, Joint Accreditation with AMA for 17.5 CME.

Physician Principal Investigator

Advanced Principal Investigator Physician Certification (APIPC)

Equip licensed physicians in their country with the knowledge and skills to undertake the role of Principal Investigator in clinical research.

Students Enrolled: 391†

Requirements: Active Medical Degree. Nonactive medical doctors, PhDs, and PharmDs can work as Sub-I with this clinical research training certification.

Length: 100 Hours. Online, self paced, start anytime.

CCRPS Reviews : View Recent Clinical Graduate Case Studies from April 2024

From Intern at a CRO to Regulatory Affairs Specialist at UPenn

From No Prior Experience to Clinical Researcher

IMG Used CCRPS to Advance as CRC, CRA, and now research project manager

Startup Associate to a Senior Clinical Research Startup Specialist

Senior Clinical Research Professional Uses CCRPS to Advance Her Career

From Pharmacist to pharmacovigilance officer with CCRPS

Drug Safety Associate used CCRPS to Transition to American Job Market

From FMG to Clinical Research Coordinator

From Clinical Research Receptionist to Certified Study Coordinator

Transitioning from Physical Therapy to Clinical Research

From PV "student" to Lead Safety Associate with CCRPS

From Educational Research to Clinical Trials Project Management

Leaders in Online, Advanced Clinical Research Certification . Comprehensive Clinical Research Training in 1 to 4 weeks. See why 22,000+ students trust us and start or advance your clinical research career today.

Clinical research courses trusted by students at 1,200+ organizations, 6 government agencies, and 308 universities. Personalized clinical research job coaching with graduates placed at 1,600+ different organizations from large CROs to various trial sites.†(2024 CCRPS Graduate Survey).

Online, self-paced, instant Linkedin badge and online certificate after passing 70% final exam. Accredited by ACCRE, Transcelerate, Joint Accreditation (AMA, ANCC, ACPE for CME), Candidate MSA for federally-qualified post-graduate institute.

Swipe to see clinical research courses ->

Clinical Research Coordinator Certification

Course Info: Salary $59k-80k. Fee $300. Requires 2 year degree. Finish in 8 days.

Graduates work at: AstraZeneca, Sloan Kettering Cancer Center, US VA, Cedars-Sinai, Mayo Clinic, Janssen, Thermo Fisher Scientific, NewYork-Presbyterian Hospital, University of Alabama, Stony Brook Medicine, NYU Langone Health, Nova Research Institute, Quest Diagnostics, Nestle, Impact H&R, and more†.

Graduate job roles post-course: Clinical Research Coordinator, Clinical Research Coordinator II, Lead Clinical Research Coordinator, Senior Clinical Research Coordinator, Oncology Research Coordinator, Clinical Study Coordinator, Clinical Research Data Coordinator, Clinical Research Nurse, Clinical Director/Office Manager, and Regulatory Contact/Clinical Research Coordinator, and more†.

Clinical Research Associate Certification

Course Info: Salary $49k-103k+. Fee $450 (payment plans available). Requires 4 year degree. Finish in 10 days.

Graduates hired at: Moderna, Merck, IQVIA, ICON plc, Eli Lilly and Company, AstraZeneca, Deloitte, Procter & Gamble, St Jude Children's, Mount Sinai, U.S. DOH HHS, Mass General Hospital, Janssen Pharma, Memorial Sloan Kettering, Stanford University, and more.†

Graduate hired as: Clinical Research Associate, Clinical Trial Monitor II, Research Associate, CRA II, Senior Clinical Research Associate, Research Associate Immunology, Clinical Trials Project Manager, Clinical Director for R&D, Clinical Research Professional, and Clinical Trial Associate III, and more.†

Pharmacovigilance and Drug Safety Certification

Course Info: Salary $59k-140k. Fee $300. 4 year degree required. Finish in 6 days.

Graduates Hired At: Novo Nordisk, Moderna, Abbott, Accenture, CVS, FDA, VA, GoodRx, Merck, NIH, MOH Ontario, Thermo Fisher Scientific, Procter & Gamble, AbbVie, Parexel, Regeneron, Bristol Myers Squibb, IQVIA, Johns Hopkins, MD Anderson, Emory Healthcare, Eli Lilly, and more.†

Graduate Hired As: Regulatory Affairs Associate, Clinical Trial Drug Safety Associate, Drug Safety Specialist, Patient Safety Senior Associate, Pharmacovigilance Scientist, Pharmacovigilance Manager, Senior Pharmacovigilance Associate, Pharmacovigilance Regional Head, Pharmacovigilance Analyst, and Senior Director Quality, and more.

ICH GCP Certification

Course Info: Most comprehensive training available for ICH GCP. Fee $50. HS diploma required. Required every 2 years. Finish in 2 days.

Graduates hired at: FDA, NHS, Novartis, Novo Nordisk, ICON PLC, PPD, IQVIA, Parexel, Johnson & Johnson, Medtronic, UNC Health, NYU Langone Health, MD Anderson, Colorado State University, Baylor, Kaiser, Cornell, Boston University, and more†.

Graduate hired as: Research Assistant, Lab Assistant, Research Coordinator, Postdoctoral Researcher, Clinical Nurse, Clinical Operations Manager, Clinical Research Assistant Professor, Clinical Research Manager, Associate Director of Clinical Development, and Vice President of Clinical Development, and more†.

Research Project Manager Certification

Course Info: Salary $65k-143k. Fee $350. Finish in 10 days. Prior PM or Research Experience required.

Graduates work at: Emory, ION Pharmaceuticals, Inc., Baim Institute for Clinical Research, Aya Healthcare, Dermavant Sciences, Inventprise, iSTAR Medical, Oregon Health & Science University, Flinders University, and more†.

Graduates hired as: Clinical Trial Project Manager, Research Nurse Manager, Clinical Research Coordinator-Data Manager, Clinical Research Associate, Transdisciplinary Research Project Manager, IT Project Manager in Clinical Research, Publicly Funded Research Project Manager, and more†.

Medical Monitor Certification

Course Info: Salary $49k-110k. Fee $350. MBBS/IMG/MD preferred. Finish in 8 days.

Graduates hired at: US Army, Yale School of Medicine, Oxford University, Merck Healthcare, IQVIA Canada, CDC Foundation, MD Anderson Cancer and more†.

Graduates hired as: Clinical Research Medical Monitor, Medical Monitor, Principal Medical Monitor, Lead Medical Monitor, Clinical Trial Medical Monitor, Associate Medical Monitor, Senior Medical Monitor, Clinical Study Physician, Medical Advisor for Clinical Research, Clinical Research Physician, Medical Safety Monitor, Medical Director of Clinical Research, Drug Safety Medical Monitor, and more†.

Principal Investigator Certification

Course Info: Fee $300. Active MD required. Salary range 42k-112k+ not including base physician salary. Finish in 6 days (optional modules).

Graduates Hired At: Accelemed Research, Zion Healthcare, CAP Research, Quotient Sciences, and more.†

Graduates Hired As: Principal Investigator in Clinical Research, Principal Research Investigator, Senior Principal Investigator, Clinical Trial Principal Investigator, Clinical Research Nurse Investigator, Oncology Principal Investigator, Radiation Therapy Principal Investigator, Academic Principal Investigator, Healthcare Settings Principal Investigator, and more.†

Research Assistant Certification

Course Info: Salary range $25k-70k+. Fee $150. HS degree required. Finish in 6 days.

Graduates work at: Various universities, hospitals, clinics, scholarships, internships, and clinical research sites.†

Graduates hired as: Clinical research assistant, clinical trial assistant, clinical researcher professional, clinical research coordinator, trial assistant, research assistant, and more†.

Clinical Research Certification Courses

Clinical Research Associate Training

Requires bachelors of science . Monitor multiple clinical trial sites. Finish in 2-4 weeks.

Pharmacovigilance Clinical Research Training

Requires bachelors of science . Monitor drug safety. Finish in 2-3 weeks.

Clinical Research Coordinator Training

Requires 2 year degree . Support a clinical trial site. Finish in 1-3 weeks.

ICH GCP Clinical Research Training

Requires HS diploma. Required for all clinical trial professionals every 2 years .

Clinical Trial Assistant Training

Requires HS diploma . Assist in clinical trials. Finish in 1-2 weeks.

Clinical Research Management Certification Training

Requires clinical trial or project management experience . Finish in 2-4 weeks.

Principal Investigator Training

Requires active MD license or pending Sub-PI position . Conduct clinical trial at site. Finish in 1-3 weeks.

Medical Monitor Training

Requires MD or MBBS/IMG/FMG . Monitor clinical trials with medical knowledge. Finish in 2-4 weeks.

Triple Accredited Clinical Research Certification Courses for 2024-2025

Transcelerate biopharma.

Recognizes CCRPS to be an accredited GCP trainer.

CCRPS is a candidate undergoing a 1 year intensive study for approval to be a federally recognized career and technical institution.

ACCRE accredits the professional program in Clinical Research leading to the Clinical Research Certification.

Institute for Credentialing Excellence

CCRPS maintains ICE organizational membership.

Upgrade your career or switch to a new path with our online clinical research training.

Joint accreditation.

CCRPS courses accredited by ACME, ICPE, and ANCC for doctors, pharmacists, and nurses for 17.5CME.

Postgraduate Institute for Medicine

CCRPS is audited by PIM for CME credit approval.

About CCRPS

Our online program for clinical research certification is trusted by thousands of students with our graduates finding careers at over 1,600 companies after taking our course per our 2024 survey. Ideal for career changers or those wanting to advance in roles like clinical research associate, coordinator, assistant, project manager, drug safety officer, principal investigator, or medical monitor.

Clinical research training courses by CCRPS are accredited by major organizations (ACCRE, Transcelerate Biopharma, AMA, ACPE, ANCC, ICPE for CME through JA) and recognized by small to large-size clinical research organizations.

Developed by senior clinical research training professionals to help students of all levels.

Training for a New Generation of Researchers

CCRPS provides affordable, industry-recognized clinical research training that will improve your job prospects and trial outcomes. We offer ICH GCP training, CRA certification, CRC certification, research assistant training, pharmacovigilance certification, PI training, medical monitor, and clinical research project manager training. We serve clinical professionals including nurses, physicians, pharmacists, PhDs, premeds, and science-field graduates who want to transition or accelerate their careers with CCRPS.

Do you want more information on our selection of clinical research training certification online programs? Read below.

Clinical Research Courses

The ICH-GCP certification is out for 2024 and offers hours worth of in depth  clinical research certification training on all aspects about Good Clinical Practice as defined by the International Conference on Harmonization. The most advanced modules provide a complete overview no matter what your background with pharmaceutical research might be; this includes ethical practices that prioritize safety along side transparent decision making processes where there are none!

Requirements for ICH GCP Certification

The only diplomas needed to enroll in this program are high school or equivalent level education (such as GED). However, if you have more training than that and would like a head start on understanding the material being taught at our college then it is recommended that prior learning be taken into consideration when scheduling classes.

Is ICH GCP Certification right for you?

The ICH-GCP clinical research certification training is a great way for anyone who needs an introduction or refresh on ICH GCP guidelines in order to be an great CCRP. Candidates appearing before interviewers may find themselves unprepared when it comes down solely and exclusively them, but this course will give you all the basics that are needed!

Download the ICH GCP guidelines .

Why choose our ICH GCP training?

ICH-GCP clinical research certification training online confers multiple benefits not matched by any other GCP certification currently available, including being E6 (R2) compliant, having instant enrollment and flexible scheduling, being industry recognized, accredited by research authorities, and affordable with flexible payment options.

Institutions such as CROs that require employees to complete GCP certification can opt for a one-time annual fee payment which allows flexible scheduling for an unlimited number of trainees.

Research Assistant - Clinical Research Assistant

The research assistant certification provides you with the kick-start that will help gain better visibility for your application. The course is designed give thorough understanding of criteria needed in order conduct them effectively, what makes one organization more desirable than another when it comes time apply. The modules cover all aspects from planning through documentation, reporting & publication as well as safety practices necessary during participant recruitment/screening procedures

Requirements for Research Assistant Certification

The research assistant training is open to anyone, even without a high school diploma or equivalent.

High school students intending to work after graduation or interested in healthcare research may benefit from completing the clinical research assistant certification.

Premed students enrolled in an undergraduate degree program and majoring in one of the life sciences may also benefit from clinical research assistant training.

Why choose our clinical research assistant certification?

The research assistant certification is the leading choice for research assistant jobs because it is fully compliant with ICH-GCP and FDA CFR, covers all key concepts extensively, has flexible scheduling, is widely recognized and accepted, and is affordable.

Is research assistant training right for you?

The research assistant program provides a strong understanding of advanced Good Clinical Practice to have a successful career with room for growth. This program offers hands-on experience in subject-facing dimensions of clinical research trials, including training in: the proper protocol for obtaining informed consent, eliciting subject cooperation during trials, obtaining necessary background information for trial documentation.

Trainees learn about subject safety monitoring, which includes exposure to: Adverse Event (AE) identification, documentation and reporting, and trial protocol adherence.

The research assistant course materials contain real-life examples and case studies to help trainees develop insight into and build strategies for: increasing subject enrollment in new and ongoing studies, improving retention rates among subjects enrolled in an ongoing study.

This advanced clinical research coordinator training program is designed to provide in-depth coverage of all aspects, from basic pharmacovigilance and regulatory audits right up through planning for scientific integrity. The course teaches students everything they need know about how best handle each situation that may arise during their career as a Clinical Research Coordinator - no matter what field area interests them most!

Requirements for CRC Certification

The clinical research coordinator (CRC) is a senior member of the clinical research team with responsibilities in overseeing the smooth conduct of clinical research. Candidates must possess a minimum of an associates degree.

Is clinical research coordinator training right for you?

The objectives of candidates enrolling in the clinical research coordinator course are typically related to advancing their clinical research careers. Research professionals enroll in the program to build the relevant knowledge base and administrative skills needed to strengthen their applications for CRC positions. Use the clinical research coordinator course refresh or upgrade their skill-set and obtain clinical research certification in coordination.

Why choose our CRC Certification?

Our clinical research coordinator training has emerged as the clear industry preference when it comes to certifying candidates for on-site roles in clinical research, due to its updated compliance information, broad and deep content coverage, flexible scheduling, and industry-wide reputation for quality.

Our clinical research coordinator certification is accredited by the ACCRE, ACCME, ACPE and ANCC - the most widely recognized and accepted CRC programs across the industry - making it a sound investment for those looking to pursue a career in clinical research.

The course tuition is affordable and can be paid up-front or in easy monthly installments

The Clinical Research Associate Program is the perfect opportunity for you to have a career in research! This advanced program has over 200 hours of specialized clinical research training, which will teach students everything they need. You'll learn how to write reports and site visits with ease using our curriculum that covers all topics related directly or indirectly toward clinical trials work--and even teaches additional techniques for efficiency and workflow.

Requirement for CRA Certification

In order to enroll for the clinical research associate certification , one must have a bachelor’s degree in life science or a health-care science, or a graduate degree in medicine.

Is CRA training right for you?

Graduates with a bachelor's degree in science who are interested in exploring clinical research can benefit from taking this course. Aspirants to CRA jobs looking to boost their hire visibility can also benefit from taking the course. Health-care professionals (RNs, NPs, PAs and others) aiming to either transition to or advance a career in clinical research.

CRAs with less than 5 years of work experience wishing to fast-track. Also, CRAs, Senior CRAs and other clinical research personnel needing a refresher course.

Why choose our CRA Certification?

The clinical research associate course confers a number of advantages on the individual, whether they are entering the field of clinical research or working to advance their career.

CRAs certified through clinical research associate training have up-to-date knowledge of both ICH and FDA regulatory requirements for human subject safety in clinical research.

The program is flexible, allowing trainees to fit the training into a busy schedule. There is an emphasis on hands-on clinical research training using real-life clinical research examples and data sets.

Completing the clinical research associate course is recognized across the US as equivalent to 17.5 CME credits.

Qualifying candidates receive not only a widely accepted and recognized clinical research associate certificate.

Pharmacovigilance

The pharmacovigilance course is an advanced program that will prepare you for a career in PV, with the most comprehensive syllabus covering all aspects from pre-clinical phase to post market surveillance (Phase IV clinical trials).

Requirements for Pharmacovigilance Clinical Research Certification

The goal of pharmacovigilance is to ensure the safety of all drugs and medical devices. QPPVs are responsible for achieving this goal through and beyond clinical trials. To be a QPPV, one must have considerable medical knowledge, statistical skill, and analytical ability. Candidates for the pharmacovigilance and regulatory affairs certification must possess a minimum of:

A bachelor’s degree in life science OR a health-care science

Is clinical research drug safety certification right for you?

The pharmacovigilance certification is beneficial for those in the clinical research field who wish to upgrade their qualifications and expertise. CTAs/CRAs, SCRAs/CRCs, medical and nursing professionals, and QPPVs can all benefit from enrolling in the program.

Enrolling in the pharmacovigilance training gives aspirants an edge when applying for positions that require advanced knowledge of PV compliance, data analytics, software management skills, medical-legal awareness, etc.

Why choose our pharmacovigilance and drug safety training?

Our drug safety and regulatory affairs course is one of the leading pharmacovigilance clinical research certification programs by recruiters across the industry. The pharmacovigilance clinical research certification is compliant with FDA CFR and WHO-ISoP, providing trainees with up-to-date coaching on all relevant regulatory codes and standards. The focus areas of the pharmacovigilance course comprehensively cover all domains of knowledge and skill required for an effective QPPV. The pharmacovigilance course trains candidates in creating, managing and retrieving case report forms using Argus Safety software. CCRPS regulatory affairs clinical research certification offers on-demand, flexible scheduling to allow enrolled students to complete the program at their own pace. The pharmacovigilance and drug safety course tuition is payable either up front or in two easy monthly installments.Explore comprehensive clinical data management training and placement opportunities in the USA. Develop your skills and secure promising positions in this dynamic field. Unlock your potential for success today.

How to Become A Trial Project Manager

Requirements for clinical trial project manager training

Clinical research project managers must have a bachelor's degree in a scientific field. We require prior clinical trial experience in managerial roles or prior project manager experience though graduates seeking to grow in their current career can take the course. They must be able to manage and coordinate all aspects of clinical trials. They must be able to keep up with ever-changing regulations governing clinical trials

Why choose our medical monitor training?

Our clinical trial project manager training is the most comprehensive and up-to-date clinical research certificate program online. You will learn how to manage clinical trials from start to finish, including budgeting, scheduling, and communication.

Upon completion of the program, you will be a certified clinical trial project manager . Our tuition rates are very affordable compared to other programs in this field.

Is project manager clinical research certification right for you?

If you're a project manager or coordinator who is looking to enhance your skills and salary, then clinical research project manager training may be right for you. Earning clinical research project manager certification can help you stand out from other project managers and improve your career prospects.

You must also pass an exam that covers topics such as risk management, stakeholder relationships and data management.

If you meet these qualifications, then becoming certified can help you demonstrate your knowledge and expertise in the field of clinical research project management . Not only will this make you a more valuable asset to your current employer, but it can also open up doors to new opportunities down the road.

Certified clinical research professionals work in a booming industry and there’s no doubt that project managers are in high demand. If you want to make the jump into clinical trial project management, or if you’re already a project manager but want to specialize in pharmaceuticals, our course is exactly what you need.

How to Become a Medical Monitor

Requirements for medical monitor training

Medical monitors are senior members of the clinical research team who oversee the ethical, safe, and transparent conduct of clinical research.

To qualify as a medical monitor, trainees must have a degree in medicine (MD), a non-US degree in medicine (IMG/FMG), or a master’s degree in pharmacy (PharmD).

Physicians with one or more years of exposure to medical research may also qualify as medical monitors.

The medical monitor certification is a program that covers the full range of knowledge domains essential for an medical monitor role, from the philosophy behind GCP to present-day regulatory requirements for clinical research. The course curriculum reflects the most updated regulatory policies related to FDA’s CFR Title 21, as well as E6 (R2) ICH-GCP guidelines. Trainees have the option of on-demand scheduling to fit with their busy schedules.

Is Medical monitor certification right for you?

The medical monitor training offers a comprehensive overview of the principles of Good Clinical Practice, as well as compliance requirements for ethical and safe medical research.

This is the only program that provides in-depth training on all aspects of clinical research design and execution.

The medical monitor course also covers pharmacovigilance concepts crucial to a medical monitor’s role such as AE/SAE identification and tracking; probabilistic assessment of AEs/SAEs as ADRs; risk management in clinical trials.

Trainees gain working knowledge of financial regulatory compliance: disclosure documentation & updating; FDA audit protocols & strategies.

An added advantage is its focus on digitized elements such remote data monitoring tools (software & video), EDC capture & quality control

Principal Investigator

The principal investigator certification program is a great way for physicians involved in clinical research who want to transition into more senior roles, enhance their eligibility when applying or overseeing trials process. It provides PIs with the ideal means of upgrading career skills while also helping them become better fundraisers and managers!

Requirements for Principal Investigator Certification

To be a certified PI, you must be a practicing physician. You may also either be the PI or Co-PI of an ongoing clinical research study, or have been the Ex-PI or former Co-PI of a completed study.

Is Principal Investigator training right for you?

The principal investigator certification provides a thorough, yet quick refresher of the regulatory and compliance requirements for ethical, safe and transparent medical research. This is an in-depth review of all aspects of leading clinical research design and execution as a principal investigator, including: advanced trial design, randomization, blinding and unblinding; clinical site assessment, preparation active site monitoring and close-out; clinical trial protocol development and implementation, including trial monitoring tools and documentation; Investigational Product (IP) accountability storage and dispensing; Adverse Events (AEs), Serious Adverse Events (SAEs), Adverse Drug Reaction (ADR), Important Medical Event (IME) – identification tracking reporting; probabilistic assessment of AEs SAEs as ADRs – medical assessment statistical data analytics risk safety assessments in clinical trials.

Why choose our PI training course?

The principal investigator certification is the best choice for both physicians who want to get certified as a PI, and for industry experts who are looking for someone to fill a PI position. This is because the certification is very flexible and covers a lot of ground.

Additionally, those who become certified principal investigators will be up-to-date on the most recent regulatory policies related to FDA CFR Title 21 and the E6 (R2) ICH-GCP guidelines. This means that they will be qualified to manage compliance requirements in a clinical study.

The course curriculum includes all of the knowledge domains essential for clinical research principal investigator training , but busy professionals can review only the modules most relevant to them and their needs. This way, they can still update their knowledge and skills without having to spend a lot of time on it.

Clinical Research Staff Training

CCRPS works with pharmaceutical, biotech, medical device, and contract research organizations to efficiently train and certify their clinical research associates, coordinators, and assistants to meet ICH GCP and CFR compliance for their staff. We can provide outsourced clinical research staff training set up within 1-2 business days. We work with organization budgets and staff training size to provide comprehensive and transformational education for onboarding and updating staff compliance with ICH GCP and job training requirements. We have worked directly with organizations and groups ranging from 2 employees to 179 employees.

The Platform for Clinical Research Education

Ccrps case studies & reviews.

From IMG to Clinical Research Coordinator at Columbia University: " This course not only met but exceeded my expectations with its thorough curriculum and insightful modules." -Lisa-Pierre ( view full case study )

From IMG to Clinical Research Coordinator "The hands-on activities integrated throughout the course really helped solidify my understanding of complex concepts." -Umber Mahmood ( case study summary )

From Physical Therapist to Clinical Researcher:  "The in-depth content and expert instructors provided me with invaluable insights into the field."  - Celia Moon ( case study summary )

From International CRC to U.S. Lead CRC and CRA:  "The flexible online format allowed me to balance my studies with my professional commitments seamlessly." - Aishwarya Sukumar  ( view full case study )

Enjoyed Clinical Research Training through Examples "The real-world examples used throughout the course were incredibly useful for applying theory to practice."  -Marta Marszalek ( view full case study )

Promoted to Senior Startup Specialist in Clinical Trials : "I appreciate how the course was structured—very interactive and engaging from start to finish." -Justin Scott Brathwaite  ( transcript summary )

From Clinical Research Receptionist to Certified Study Coordinator with CCRPS:  "I highly recommend this course for its comprehensive approach and practical applications."  - Katie Decker ( view full case study ) 

Learning to Lead Safety Associate: "The course materials were clear, well-organized, and directly applicable to my work." - Renata Noronha ( view full case study )

From IMG to securing roles as a CRC, CRA, and now a project manager: "Joining this course was a pivotal step in my career advancement."  - Dr. Vrushali Borawak ( view full case study )

From Physician to Confident Drug Safety Specialist:  "The course provided a robust foundation in the field, which was critical for my professional development." - Rabiea Bilal ( view full case study )

From plant biologist to clinical recruitment administrative coordinator : "This program is a gateway to extensive knowledge and skills in a supportive learning environment." -Olajumoke Owati ( view full case study )

ICH GCP Expert:   "Thanks to this course, I feel more competent and confident in my role." - Stephanie ( case study summary )

From International PV Roles To North American Market Success: "The detailed modules prepared me excellently for real-world applications." - John Vinil ( view full case study )

From Educational Research to Clinical Trials Project Management:   "I was able to immediately apply what I learned in the course to my job. " - Rose Hyson ( view full case study )

From Coordinator to Clinical Research Grant Manager:  "it really did a great job of the full scope of clinical research from start to finish."  -Hannah Fischer

ICH GCP made her more confident in research:  "this course just overall did a really good job going in depth, which I feel like wasn't just, it wasn't just covered just for the sake of covering content" -  Aastha Shah  (view full transcript)

From Clinical Research Intern to Regulatory Affairs Associate at UPenn: "I would say since then. I've completed this course. It's helped me get my job in regulatory affairs at a clinical research site." - Scott Boyle

From Masters in Health Safety to Clinical Researcher:  " I will say quality of delivery, quality of the materials.   - Ossai Opene  ( view full case study )