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Senior Medical Affairs Director

2 months ago

London, Greater London, United Kingdom IQVIA Full time
Job Description

Company Overview

IQVIA is a leading healthcare technology and consulting company that provides innovative solutions to the life sciences industry.

Job Summary

We are seeking an experienced Senior Medical Affairs leader to join our client's team, specializing in one specific rare disease area. This pivotal role carries responsibility for building out and leading the company's medical affairs team as they increase their EU footprint and will likely expand to include other rare disease programs under development in future.

Key Responsibilities

  • Build and lead a high-calibre EU Medical Affairs team, collaborating with partners and internal teams to ensure successful product development, launch, and lifecycle management.
  • Develop and execute Medical Affairs strategies, represent the company in regulatory interactions, and establish centres of excellence for relevant conditions.
  • Engage with key opinion leaders, physicians, and patient groups, and work cross-functionally to advance medical aspects of the company's activities.

Requirements

  • Strong background at a senior level of building and leading a Medical Affairs team in Europe, especially during late-stage development and launch phase.
  • Experience: 10-15 years in the medical department of a pharmaceutical or biotech company, with experience in rare diseases and orphan drugs, combined with at least 8 years of international experience.
  • Medical Background: Must have Hospital experience as a practicing doctor and General Medical Council UK registration or equivalent medical qualification.
  • Comprehensive understanding of industry medical governance norms and compliance with laws, regulations, and codes of practice.
  • Location: Must be UK based, with the willingness and ability to work from the company's HQ in London 3 days per week.

Desirable Skills

  • Proven ability to add value and influence global medical strategy, engage stakeholders with integrity, and communicate effectively across various media.
  • Skilled in medico-legal review processes, scientific communication, and have a solid understanding of EU medical information and pharmacovigilance practices.