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Clinical Trial Associate or Senior Clinical Trial Associate

Watertown, MA💼 Full-time💰 $115,000–$115,000🗓 2026-09-15 → 2026-10-01

Core

Manage the planning, execution, and delivery of global clinical trials for a clinical-stage biotech company developing targeted protein degradation medicines.

Role type

Senior Clinical Trial Manager (IC)

Builds

Global clinical trial programs for oral small molecule degraders

Domain

Biotechnology / Clinical Development

Required skills

Clinical trial management, vendor management, study design input, site selection and monitoring, data integrity management, protocol deviation tracking, cross-functional collaboration

Preferred skills

Experience with Phase 2 trials, bioanalytical sampling plan integration

Technologies

eCRFs, monitoring conventions, edit checks

Responsibilities

Plan and execute global clinical trials; manage vendors; lead study-specific meetings; provide training to clinical staff and CROs; manage study timelines and metrics; support site selection and monitoring; review monitoring reports; ensure timely enrollment and data collection; collaborate with data management; analyze trial data; track protocol deviations; develop investigator relationships; ensure safety and efficacy data summary; incorporate bioanalytical sampling plans; maintain trial documentation.

Seniority

Senior, hands-on IC

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