Full course description
Clinical trial managers are now working closely with other groups within a clinical trial to ensure that data us collected, managed, and reported in a timely manner, accurately, and securely. Therefore the clinical trial manager must understand good clinical practices, protocol, protocol deviations, metadata, basic SDTM mapping, programming, and Excel. Therefore building the skills of clinical trial managers is essential
After the course, participants should be able to:
- Core concepts in bioethics, including well-being, justice, and autonomy
- Skills required to discuss the bioethics topics such as abortion and euthanasia
- Key bioethics terms such as informed consent and medical futility
- Skills required to evaluate the ethical principles relevant to clinical research
Teaching: The course will be taught through series of online tutorials, online formative exercises, series of pod-casts and discussion forums. It is compulsory that student take part in 90% of online tutorials. Self-directed learning is an essential component of this training. Electronic learning resources will be made available via our VLE.
Learning breakdown: Our online courses combine several elements to create a balanced blend of learning. Learners will be able to learn at their own pace during the week by viewing content, engaged in discussions, and completing assignments. It is expected that on the average, 8 to 10 hours per week is required for a course.
Assessment: Assessment for this course is based on summative assessment which counts to the module mark. Each summative assessment for a module will be made of a 1000 word essay, scientific article of high standard, 15 minutes presentations, and 3000 worded final assignment.
Duration: 12 weeks
Commitment: 8-10 hours per week as follows:
Projected time (Hours)
Eligibility: The course is designed for:
Graduate or have successfully completed a professional course
Individuals with professional work experience in health-related institute