Job Description
Join MedTech Innovations at the forefront of medical breakthroughs. We're seeking a Clinical Research Coordinator to drive life-changing studies in oncology and cardiology. You'll collaborate with leading physicians, manage complex protocols, and ensure regulatory compliance while contributing to FDA-approved therapies. Our state-of-the-art Boston facility offers cutting-edge labs and a collaborative culture focused on patient-centered innovation. Enjoy competitive benefits, flexible scheduling, and opportunities for continuing education.
Responsibilities
- Oversee clinical trial protocols from initiation to closure, ensuring FDA/ICH-GCP compliance
- Recruit, screen, and maintain relationships with study participants across diverse demographics
- Manage electronic data capture systems and maintain accurate regulatory documentation
- Coordinate interdisciplinary teams including physicians, nurses, and biostatisticians
- Monitor adverse events and ensure timely safety reporting to IRB and sponsors
- Prepare regulatory submissions and manage trial budgets and vendor contracts
Qualifications
- Bachelor's degree in Nursing, Life Sciences, or related field (Master's preferred)
- 2+ years clinical research coordination experience in oncology/cardiology trials
- Certified Clinical Research Professional (CCRP) or SOCRA certification required
- Proficiency in REDCap, Medidata Rave, and CTMS platforms
- Demonstrated knowledge of 21 CFR Parts 11, 56, and 312 regulations
- Exceptional organizational skills with ability to manage multiple concurrent studies
- Strong interpersonal skills for patient communication and team collaboration