Job Description
Join our prestigious medical research institute at the forefront of groundbreaking clinical trials. As a Senior Clinical Research Coordinator, you'll lead complex studies while mentoring junior staff and ensuring regulatory compliance. We offer competitive compensation, comprehensive benefits, and opportunities for professional growth in a cutting-edge environment.
Responsibilities
- Design and oversee implementation of multi-center clinical trials
- Ensure FDA/ICH GCP compliance and protocol adherence
- Manage study budgets, timelines, and resource allocation
- Lead investigator meetings and regulatory submissions
- Mentor and train junior research coordinators
- Analyze clinical data and prepare regulatory documentation
- Collaborate with pharmaceutical partners and ethics committees
Qualifications
- Master's degree in clinical research, nursing, or related field
- 5+ years of clinical trial coordination experience
- Certified Clinical Research Professional (CCRP) preferred
- Expertise in oncology or immunology trials
- Strong proficiency in EDC systems (e.g., Medidata Rave)
- Exceptional regulatory and documentation skills
- Proven leadership and mentoring abilities
- Excellent communication and problem-solving skills