Clinical Research Coordinator

Role Overview: As a Clinical Research Coordinator, your primary responsibility will be to recruit and enroll study participants for research projects. You will 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. Ensuring compliance with all local and federal laws and regulations at the study site will be part of your duties. Additionally, you will create comprehensive documentation of study protocols and update them as needed. Coordinating with study sites, sponsors, ethics committees, and Principal Investigators for the smooth conduct of the study is also expected. Key Responsibilities: - Recruit and enroll study participants for research projects - Input clinical research data into electronic data systems - Coordinate patient visits and procedures - Address inquiries and explain procedures to study participants - Ensure compliance with local and federal laws and regulations - Create and update comprehensive documentation of study protocols - Coordinate with study sites, sponsors, ethics committees, and Principal Investigators Qualifications Required: - Bachelor of Science or Master of Science in fields such as biotechnology, biochemistry, microbiology, biology, nursing, pharmacy, or basic life sciences - Diploma in clinical research - 2-5 years of prior clinical research experience preferred - Strong analytical and creative thinking skills - Advanced organizational and planning abilities - Proficiency in MS Word and Excel programs,