Clinical Research Registered Nurse - RN - Oncology
About The Position
At Trinity Health Of New England, the Clinical Research Registered Nurse and play a key role in advancing cancer care through innovative clinical trials. In this position, you will coordinate oncology research studies, collaborate with physicians and research teams, monitor patient safety, manage regulatory documentation, and support participants throughout the clinical trial process. Trinity Health Of New England is collaborating with Dana-Farber Cancer Institute to strengthen and expand cancer care across the region. This relationship combines Dana-Farber’s nationally recognized oncology expertise with Trinity Health Of New England’s commitment to delivering exceptional, locally led care close to home. Through access to clinical specialists, tumor boards, educational resources and best practices, patients and providers will benefit from enhanced support and innovation. Together, we are building a stronger, more integrated oncology program focused on clinical excellence and outstanding patient outcomes. Rooted in our Mission and Core Values, we honor the dignity of every person and recognize the unique perspectives, experiences, and talents each colleague brings. By finding common ground and embracing our differences, we grow stronger together and deliver more compassionate, person-centered care. We are an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or any other status protected by federal, state, or local law.
Requirements
- Graduate of an accredited School of Nursing.
- Current Registered Nurse (RN) licensure for Connecticut.
Nice To Haves
- Bachelor of Science in Nursing (BSN) preferred.
- Clinical Research certification through ACRP, SOCRA, or equivalent professional organization preferred.
- Clinical research experience in an academic medical center, healthcare system, or industry-sponsored environment preferred.
- Experience coordinating clinical trials and regulatory submissions preferred.
Responsibilities
- Coordinate clinical research studies from start-up through closeout
- Collaborate with investigators, sponsors, and interdisciplinary teams
- Perform protocol-required clinical assessments and procedures
- Monitor participant safety and report adverse events
- Manage informed consent, regulatory documentation, and study data
- Educate participants and families on research studies and procedures
Benefits
- Great benefits from Day 1
- Patient-centric environment
- Career growth and advancement potential
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Education Level
Associate degree
