Associate Medical Director, Clinical Research
Core
Design, plan, execute, and interpret clinical trial activities for novel oncology compounds from early development to global regulatory submissions.
Role type
Associate Medical Director, Clinical Development (Oncology)
Builds
Clinical protocols, regulatory filings (INDs, NDAs), and clinical study data for oncology therapies.
Domain
Pharmaceutical / Oncology / Clinical Research
Required skills
Clinical trial design and implementation, medical and scientific leadership, regulatory document authoring, safety and efficacy data interpretation, investigator relations, manuscript authoring, cross-functional collaboration
Preferred skills
Hematological malignancies expertise, solid tumors experience, subspecialty fellowship, residency completion
Technologies
Clinical trial management systems, regulatory filing platforms
Responsibilities
Lead clinical study teams and monitor study integrity, respond to site questions on eligibility and dose modification, present at global scientific and regulatory meetings, partner with drug safety and pharmacovigilance, author clinical sections for regulatory submissions, maintain relationships with academic investigators and KOLs
Seniority
Senior, hands-on IC