Clinical trial online courses

Top Clinical Trials Courses - Learn Clinical Trials Online Coursera Browse Related topics: clinical research clinical biostatistics drug drugs spss 19 results for "clinical trials" Design and Interpretation of Clinical Trials Johns Hopkins University Course 4.7(3,823) 120k students Mixed Clinical Data Science University of Colorado System


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Clinical trials play a pivotal role in evidence-based medicine. This course will discuss the design, conduct, analysis, and interpretation of Phase I-IV clinical studies. Add to list Quick View edX 4-6 hours a week, 4 weeks long Finished Free Online Course (Audit) Designing and Analyzing Clinical Trials in R


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Clinical Trials Courses Harvard University Clinical Trials Courses 1 results Health & Medicine Online Immuno-oncology See how the immune system is being used to improve cancer treatment. $800 10 weeks long Register by May 17


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100% online Start instantly and learn at your own schedule. Approx. 10 hours to complete English Subtitles: Arabic, French, Portuguese (European), Italian, Vietnamese, German, Russian, English, Spanish Skills you will gain Clinical Research Trial Design Clinical Trial Design Clinical Trial Management Offered by Johns Hopkins University

Rating: 4.7/5(637)
End date: Jun 06, 2022
Start Date: Apr 18, 2022


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The Clinical Trials Management Online Certificate is offered 100% online and provides a broad overview of key competencies necessary for a successful understanding and conduct of the new product development process in today’s environment. Course topics include: Clinical trials process, roles and responsibilities U.S. regulatory compliance

Estimated Reading Time: 9 mins


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This course provides the foundational knowledge upon which one can develop his/her competence as a clinical research professional. This two-hour online course details how medical products are developed, how volunteer patients are protected, and who plays key roles in the development, research, review, and approval of medical products.


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These online courses offer affordable, convenient access to quality education. SOCRA's online courses are intended to provide access to training and continuing education that will promote quality clinical research, protect the welfare of research participants and improve global health. Part I - Informed Consent for Research Laura Holtz, MS, CCRP


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The 100-hour ACTAC program comprises over 25 modules that provide a thorough overview of the basics of how clinical trials are planned, conducted, documented and reported. Through the course, trainees learn the principles behind scientific and ethical medical research.


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The Office of Clinical Research has the responsibility for courses which provide clinical research training for the spectrum of investigators and others involved in clinical research. Introduction to the Principles and Practice of Clinical Research Principles of Clinical Pharmacology Ethical and Regulatory Aspects of Clinical Research


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Write clinical trial and IRB protocols; Requirements. Students must complete a total of 15 credits (5 courses) and attend a total of 6 colloquia over the course of their studies. The program starts in January or September and completes in one year. Required Courses. 16:137:510 Drug Development from Concept to Market (3 cr)


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This certificate program focuses primarily on the design and analysis of randomized clinical trials for evaluation of licensed and non-licensed medical products and other health interventions, the regulatory framework for the conduct and evaluation of data from clinical trials, and ethical principles for the conduct of clinical trials.


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Virtual ACRP 2021 Innovation in the Era of COVID Track Replay. Unlock your potential by learning innovative new ways clinical research is being conducted in response to COVID-19. This online, interactive program addresses telemedicine, remote monitoring, team management, study start-up and more in the era of COVID.


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The course focuses on the spectrum of clinical research and the research process by highlighting biostatistical and epidemiologic methods, study design, protocol preparation, patient monitoring, quality assurance, ethical and legal issues, and much more. Course Objectives


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As good as free online clinical research courses are to help you develop your career as a clinical research professional, they are not meant to take the place of the required training needed, especially those that train you in the protection of the human subjects of clinical research. For further details and information on how to get free


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Document your dedication to compliance, safety, and job performance by earning a professional certification from Biopharma Institute. Biopharma Institute offers a catalog of over 200 programs for pharmaceutical, medical device, and clinical research professionals. Below is our list of Clinical Trials Management and Monitoring training courses


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Live Online In-Person Online Hybrid Download PDF Prerequisites Medical Terminology: An Anatomy and Physiology Approach FPM-40632 Units: 1.50 $295 Required Courses CT: Drug Development Process FPM-40173 Units: 3.00 $595 CT: Human Subjects Protection and IRBs FPM-40388 Units: 2.00 $475 CT: Good Clinical Practices FPM-40204 Units: 3.00 $595 Electives


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This course focuses on the theoretical underpinnings of clinical research and the practical aspects of conducting clinical trials: the rationale for design features of Phase I, II, and III trials, recruitment of participants, techniques for randomization, data collection and endpoints, interim monitoring, and results reporting. Experts will deliver lectures on such topics as pitfalls in …


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Frequently Asked Questions

Is GCP training required?

Good Clinical Practice (GCP) training is required for all research personnel involved in the conduct, management and oversight of a clinical trial at Lurie Children's, additionally it may be required by sponsors or funding agencies.

How do I become a clinical research associate?

  • Monitor clinical trials and take notes on activities
  • Ensure compliance with all clinical trial protocols
  • Enter clinical research data into appropriate fields
  • Transfer data from paper formats via computer, recorders, or scanners
  • Organize spreadsheets with large numbers
  • Curate data directly from clinical research
  • Oversee clinical site activities

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What is a Masters in clinical research?

  • Expertise and Involvement in the Field, as determined by membership in the Consortium of Academic Programs in Clinical Research.
  • Career Training and Curricular Relevance, as determined by the balance of clinical and managerial coursework.
  • Accessibility to Students, as determined by the academic and professional experience required for admission.

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