Clinical Research Coordinator

As a Clinical Research Coordinator, your primary responsibility will be to recruit and enrol study participants for research projects. You will be required to input clinical research data into electronic data systems, coordinate patient visits and procedures, and act as a resource for study participants by addressing their inquiries and explaining related procedures. It will also be your duty to ensure that the study site complies with all local and federal laws and regulations. In addition, you will be responsible for creating comprehensive documentation of study protocols and updating them as necessary. Proper archival of case report forms and related documents will be part of your routine tasks. You will also be expected to coordinate with all study sites, as well as with the sponsor, ethics committee, and Principal Investigator to ensure the smooth conduct of the study. The ideal candidate for this role would be a graduate with a Bachelor of Science or a Master of Science in fields such as biotechnology, biochemistry, microbiology, biology, nursing, pharmacy, or basic life sciences, along with a Diploma in clinical research. A minimum of 2-5 years of prior clinical research experience is preferred. Strong analytical and creative thinking skills, advanced organizational and planning abilities, as well as proficiency in MS Word and Excel programs are essential for this position.,