Support study documents: schedules, endpoints, and criteria.
Contribute to authoring/review of study protocols and supporting docs.
Prepare materials for regulatory response packages.
Provide protocol/study training to internal teams and CRO partners.
Ensure manuals and CRFs align with protocol requirements.
Participate in study meetings, site initiation visits, and investigator meetings.

🎯 Requirements

Advanced degree preferred (MS, RN, or PhD)
2–4 years in clinical research or clinical science
Experience with clinical data review and interpretation
Oncology/early detection knowledge a plus
Basic understanding of study protocols and CRFs
Scientific writing experience helpful

🎁 Benefits

Medical, dental, vision, life and disability coverage
Fertility care benefits and family leave options
401k retirement plan
Commuter benefits
Employee referral program

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