Job Description
Join our pioneering team at MediVance Innovations, where cutting-edge research meets compassionate patient care. We're seeking a Senior Clinical Research Coordinator to drive critical medical trials that transform healthcare outcomes. In this role, you'll manage complex oncology studies while collaborating with top-tier physicians and biotech partners.
We offer a collaborative environment with competitive benefits, professional development stipends, and the opportunity to contribute to life-changing therapies. Our Boston headquarters is steps from world-class medical institutions and features state-of-the-art research facilities.
Responsibilities
- Design and oversee clinical trial protocols in oncology research
- Coordinate multi-site patient recruitment and retention strategies
- Ensure strict compliance with FDA regulations and GCP standards
- Manage electronic data capture systems and regulatory documentation
- Liaise between investigative sites, sponsors, and ethics committees
- Mentor junior research staff and conduct protocol training
- Analyze trial data and prepare regulatory submissions
Qualifications
- Master's degree in Clinical Research, Nursing, or related field
- Certified Clinical Research Professional (CCRP) required
- Minimum 5 years oncology clinical trial coordination experience
- Proven expertise in FDA 1572 and ICH-GCP compliance
- Advanced proficiency in clinical trial management systems (e.g., Medidata Rave)
- Strong budget management and vendor negotiation skills
- Excellent written communication for protocol development
- Experience with oncology-specific AE grading (CTCAE v5)