Job Description
Join our pioneering medical research team at MediCore Solutions, where innovation meets compassionate care. We're seeking a meticulous Clinical Research Coordinator to drive critical clinical trials that shape the future of medicine. This role offers the opportunity to work alongside leading physicians and scientists in state-of-the-art facilities while contributing to life-altering medical breakthroughs.
Our Boston-based center combines cutting-edge technology with a patient-first philosophy, offering unparalleled career growth and competitive benefits including comprehensive health insurance, 401(k) matching, and professional development stipends. You'll be part of a collaborative environment that values precision, ethical integrity, and scientific excellence.
Responsibilities
- Oversee all aspects of clinical trial protocols including patient recruitment, enrollment, and retention strategies
- Ensure strict adherence to FDA regulations, ICH-GCP guidelines, and institutional IRB protocols
- Manage comprehensive trial documentation including case report forms, informed consent processes, and regulatory submissions
- Coordinate multidisciplinary research teams including physicians, nurses, and data specialists
- Monitor patient safety and adverse event reporting systems with real-time documentation
- Analyze and interpret clinical data using specialized statistical software platforms
- Present research findings at scientific conferences and peer-reviewed publications
Qualifications
- Master's degree in Clinical Research, Nursing, Life Sciences, or related field (Bachelor's with 5+ years experience considered)
- Certified Clinical Research Professional (CCRP) or SOCRA certification required
- Minimum 3 years coordinating clinical trials in therapeutic areas (oncology/neurology preferred)
- Expertise in electronic data capture systems (e.g., Medidata Rave, Oracle Inform)
- Proven track record in maintaining 100% audit-ready documentation
- Strong statistical literacy with experience in SAS or R programming
- Exceptional attention to detail with ability to manage complex regulatory requirements