Director, Global Regulatory Affairs & Clinical Safety Business Development

Merck·LinkedIn
Rahway, NJFULL_TIMEPosted Jul 2, 2026
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Role responsibilities

The Director will oversee staff managing business development stages related to regulatory affairs. This includes strategy, evaluation, due diligence, contracting, and maintaining regulatory activities for various transactions.

Requirements

A bachelor's degree is required, along with at least 7 years of experience in the pharmaceutical industry or a related field. An advanced degree in a relevant discipline is preferred.

Key skills

Adaptability, Change Management, Detail-Oriented, Regulatory Affairs Management, Regulatory Compliance, Regulatory Compliance Audits, Regulatory Experience, Regulatory Strategy Development, Regulatory Submissions, Strategic Planning, Strategic Thinking

Keywords

Regulatory Affairs, Business Development, Pharmaceutical Industry, Mergers, Acquisitions, In-Licensing, Collaborations, Employee Development, Negotiation, Agreements, Product Acquisitions, Distribution, Co-Marketing, Co-Promotion, Tech Transfer, Joint Ventures, Divestitures, Due Diligence, Contracting, Implementation Support

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