CareerPlan

Director, Clinical Trial Management

Cincinnati, OhioFull-time2026-07-17 → 2026-11-11
On-site

Core

Lead day-to-day operations of clinical trials for biotech and pharma clients, ensuring compliance with ICH/GCP and managing project timelines, risks, and vendors.

Role type

Senior IC clinical trial management director

Builds

Clinical trial projects for biotechnology, pharmaceutical, and medical device industries

Domain

Clinical research / Biopharma

Required skills

Clinical trial management, protocol development, risk assessment, vendor management, site quality monitoring, bid defense, cross-functional leadership

Preferred skills

Advanced degree in health-related field, experience in Phases 2-3 clinical trials

Technologies

ICH/GCP regulations, clinical trial software platforms

Responsibilities

Manage and provide accountability for day-to-day operations of the project, Serve as primary Sponsor contact for operational project-specific issues, Review and provide input for study protocol and final study report, Develop operational project plans, Manage risk assessment and execution, Manage study vendors and site quality monitoring deliverables

Seniority

Director, strategic oversight & hands-on management