Oncology Research Regulatory Coodinator
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At a glance
Job overview
The Oncology Research Regulatory Coordinator reports to the Oncology Clinical Research Manager and coordinates regulatory activities for clinical research studies, supporting protocol submissions, preparing regulatory documents, and maintaining study records to ensure compliance with Trinity Health policies, federal regulations, and ICH/GCP guidelines.
Full job description
Employment Type: Full timeShift: Day Shift Description: The Oncology Research Regulatory Coordinator (RC) reports to the Oncology Clinical Research Manager and is responsible for coordinating regulatory activities for clinical research studies. This role supports protocol submissions, regulatory document preparation, and maintenance of study records to ensure compliance with Trinity Health Of New England policies, federal regulations, and ICH/GCP guidelines.
This is a hybrid position requiring a combination of remote and onsite work based on departmental and organizational needs, as determined by the Clinical Research Manager.
Our Commitment
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.
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