Director, Global Regulatory Affairs & Clinical Safety Business Development

Role responsibilities

The Director will oversee staff managing business development stages related to regulatory affairs for various transactions. Responsibilities include employee development, strategy management, and collaboration across functional areas.

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, Clinical Safety, Business Development, Pharmaceutical Industry, Mergers, Acquisitions, In-Licensing, Collaborations, Employee Development, Negotiation, Regulatory Components, Product Acquisitions, Distribution, Co-Marketing, Co-Promotion, Tech Transfer, Joint Ventures, Divestitures, Due Diligence, Contracting, Implementation Support, Regulatory Activities, Strategy, Evaluation, Maintenance, Problem Solving, Integration Points, Fast Paced Timelines, Health Authority, Regulatory Compliance Audits