Job Description

Senior Manager in Medical Affairs at Becton Dickinson will lead clinical trial program staff and activities, manage site monitoring, and oversee regulatory compliance across assigned projects in Franklin Lakes, New Jersey.

Responsibilities

• Lead and manage EP program staff, contractors, and vendor personnel on services and procedures
• Hire, evaluate, and oversee associates and vendors engaged in program activities
• Handle all IRB and Ethics Committee submissions and communications
• Monitor assigned clinical sites and projects; ensure protocol compliance with GCP/ISO standards
• Maintain audit-ready regulatory files and ensure subject safety and informed consent procedures

Requirements

• Licensed healthcare practitioner (RN, PA, NP) with Bachelor's degree in science-related field
• Minimum 5 years experience in human clinical trials with GCP knowledge
• Minimum 5 years program management and people management experience
• Minimum 3 years site monitoring experience preferred
• Clinical trial management certification from recognized entity preferred
• Strong communication, presentation, and analytical writing skills
• Ability to lead cross-functional teams and work independently

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