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In Vivo PK/PD Coordinator

Groton, CT, us💼 Full-time💰 $65,000–$65,000🗓 2026-09-16 → 2026-09-26

Core

Coordinate external in vivo PK, PD, and PK/PD studies for client drug discovery portfolios by acting as a liaison between internal teams and CROs.

Role type

Senior In Vivo PK/PD Coordinator

Builds

External study workflows and data packages for drug discovery programs

Domain

Biopharmaceuticals / Preclinical Drug Discovery

Deliverable

client delivery

Required skills

In vivo PK/PD expertise, CRO management, study protocol design, risk identification, workflow tracking, scientific judgment

Preferred skills

Small molecule/peptide/large molecule PK experience, in vitro biology workflows, reagent provision

Technologies

None stated

Responsibilities

Coordinate external in vivo PK, PD, and PK/PD studies at CROs; Ensure compliance with external PK workflow and study requirements; Participate in devising study approach, dose selection, sampling strategy, and endpoints; Facilitate alignment on objectives, deliverables, and timelines; Review proposals, protocols, and data packages; Identify risks and resolve barriers; Track requests and manage logistics including KPIs

Seniority

Senior, hands-on IC

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