Clinical Research Coordinator

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 experience
• Must possess superior analytical and creative thinking skills
• Advanced organizational and planning skills
• Proficiency in MS Word and Excel programs