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Medical Director, Clinical Development

USA - Pennsylvania - Plymouth Meeting🌐 Remote💼 Full-time💰 $204,100–$204,100🗓 2026-09-10 → 2026-09-26

Core

Lead protocol design, scientific oversight, and regulatory strategy for clinical research studies involving new or marketed drugs.

Role type

Senior Medical Director, Clinical Development

Builds

Global clinical development plans, clinical trial protocols, regulatory submission dossiers, and CSR reports

Domain

Biopharmaceuticals / Clinical Development / Women's Health

Deliverable

production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work

Required skills

Protocol design, clinical trial execution oversight, regulatory strategy, data interpretation, medical monitoring, stakeholder collaboration, strategic planning

Preferred skills

Women's health, dermatology, or pediatric development experience; academic research leadership; investigator experience

Technologies

ICH guidelines, GCP, clinical trial execution platforms

Responsibilities

Design patient-centered clinical protocols; monitor study conduct and safety; collaborate on regulatory submissions; interpret efficacy and safety data; lead investigator meetings; build relationships with external thought leaders and patient advocacy groups

Seniority

Senior, hands-on IC with strategic oversight

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