Job Responsibilities
- Recruit and enrol study participants
- Input clinical research data into electronic data systems
- Coordinate patient visits and procedures related to research
- Act as a resource for study participants by answering questions and explaining related procedures
- Ensure the study site complies with all local and federal laws and regulations
- Create thorough documentation of study protocol and update it as needed
- Proper archival of case report forms and related documents.
- Coordination with all study sites.
- Coordination with the sponsor, ethics committee and PI for smooth conduct of study
Preferred Work Experience
Graduates with a Bachelor of Science or a Master of Science in areas such as biotechnology, biochemistry, microbiology and biology, Nursing and Pharmacy or basic life science. With the additional qualification of Diploma in clinical research.2-5 years of prior clinical research experienceMust possess superior analytical and creative thinking skillsAdvanced organizational and planning skillsProficiency in MS Word and Excel programsSkills Required
Clinical Research, Ms Word, Excel