Job Description
Are you ready to be at the forefront of medical innovation? Beacon Hill Medical Research Center is seeking a high-caliber Senior Clinical Research Nurse Coordinator to join our elite oncology trials team in Boston. In this pivotal role, you will bridge the gap between groundbreaking laboratory science and life-saving patient care.
Our facility is a global leader in Phase II and III clinical trials, providing an environment where professional excellence meets compassionate care. We offer a sophisticated workplace culture, state-of-the-art resources, and a commitment to work-life balance that is unmatched in the healthcare industry. If you are a dedicated RN with a passion for research and clinical excellence, we invite you to advance your career with us.
Responsibilities
- Lead the end-to-end coordination of complex Phase II and III clinical trials, ensuring strict adherence to ICH-GCP guidelines and study protocols.
- Execute strategic patient recruitment and retention plans, performing detailed screenings and managing the enrollment lifecycle.
- Collaborate directly with Principal Investigators to analyze clinical data and optimize patient care strategies within the research framework.
- Serve as the primary liaison between clinical sponsors, regulatory bodies (FDA/IRB), and the internal medical team to ensure data integrity.
- Conduct comprehensive clinical assessments and administer investigational products, monitoring for adverse events and efficacy.
- Mentor junior research staff and contribute to the development of Standard Operating Procedures (SOPs) for the research department.
Qualifications
- Active and unrestricted Registered Nurse (RN) license in the Commonwealth of Massachusetts.
- Bachelor of Science in Nursing (BSN) is required; MSN or relevant Master’s degree is a distinct advantage.
- Minimum of 5 years of clinical experience, with at least 3 years dedicated specifically to clinical research coordination.
- Certified Clinical Research Coordinator (CCRC) or CCRP certification is highly preferred.
- Expertise in oncology clinical trials and familiarity with Electronic Data Capture (EDC) and EHR systems.
- Profound understanding of FDA regulations, HIPAA compliance, and the Protection of Human Subjects.
- Exceptional analytical thinking and the ability to manage multiple complex projects simultaneously.