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Clinical Development Medical Director (MD required)

United States - New York - Pearl River💼 Full-time💰 $239,900–$239,900🗓 2026-09-25 → 2026-09-29

Core

Provide medical and scientific oversight for clinical trials, ensuring patient safety, designing study strategies, and managing data integrity for pharmaceutical compounds.

Role type

Senior IC Clinical Development Medical Director

Builds

Clinical studies and regulatory documents for worldwide approval

Domain

Pharmaceutical industry + Clinical Research

Required skills

Medical degree (M.D./D.O.), clinical trial design, safety surveillance, regulatory compliance, data analysis, stakeholder management, leadership

Preferred skills

Statistics knowledge, infectious diseases experience, investigational trial experience

Technologies

ClinicalTrials.gov, EudraCT, Pfizer.com

Responsibilities

Monitor study safety issues and review individual/cumulative safety data; Design clinical studies to meet objectives and ensure regulatory compliance; Provide medical input to protocol teams and vendors; Author clinical sections of regulatory documents; Interact with regulatory authorities and key opinion leaders.

Seniority

Senior, hands-on IC with leadership capabilities

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