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 experience
Must possess superior analytical and creative thinking skills
