Senior Manager, Global Medical Affairs

1w1 week ago

Theramex

London, GB · Full-time · £85,000 – £120,000

About this role

We are seeking a highly motivated and experienced Senior Manager, Global Medical Affairs to join our dynamic team at Theramex. This role is pivotal in providing subject matter knowledge and expertise, developing the global medical affairs strategy and programs, and supporting product lifecycle management. You will ensure the highest standards of compliance, ethics, and patient safety while working cross-functionally.

You will develop and implement medical plans aligned with business objectives and manage associated budgets. Provide expert medical input across the product lifecycle, including evidence generation, dissemination through health care professional education programs, and medical experts’ engagement programs like advisory boards. Build relationships with international therapy area experts and professional societies.

Act as a medical reviewer for promotional and non-promotional materials in line with ABPI and international codes as well as internal SOPs. Support regulatory and market access submissions with clinical content while ensuring compliance and operational excellence. Contribute to continuous process improvement in a fast-paced environment focused on women's health.

Be part of a dynamic team where you gain broad exposure and develop professionally, even outside your area of expertise. Theramex supports growth and learning, celebrates success, and recognizes performance. Join opportunities for driven professionals on our exciting journey making a significant impact.

Requirements

Medical degree with GMC registration or equivalent international qualification or Master of Pharmacy with GPhC registration
Previous experience in Medical Affairs, Clinical Research, or Pharmacovigilance within the pharmaceutical industry
Very good understanding of Medical Affairs’ role as scientific enabler and strategic partner in a pharmaceutical company
Strong knowledge and subject matter in women’s health
Ability to cut through scientific complexity and to communicate precisely and clearly with different target audiences
Strong interpersonal and leadership skills and track record of expertise working in a cross-functional environment
Strong analytical and strategic thinking
Proven knowledge of the ABPI Code of Practice and codes of international associations of the pharmaceutical industry, with experience in reviewing and/or certifying materials

Responsibilities

Develop and implement medical plans aligned with business objectives and manage associated budgets
Provide expert medical input across the product lifecycle, including evidence generation
Provide expert medical input across the product lifecycle, including evidence dissemination (e.g. health care professional education programs)
Provide expert medical input across the product lifecycle, including medical experts’ engagement programs (e.g. advisory boards)
Build and maintain relationships with international therapy area experts and medical-scientific professional societies
Act as a medical reviewer for promotional and non-promotional materials in line with the ABPI and international associations of the pharmaceutical industry codes as well as internal SOPs
Support regulatory and market access submissions with clinical content
Ensure compliance with all relevant regulations and contribute to continuous process improvement

Benefits

Fast-paced environment with broad exposure where you can develop professionally – even outside your area of expertise
Support as you grow and learn, with celebration of success and recognition of performance
Opportunities for driven and talented professionals who want to be part of our exciting journey
Make a significant impact on women's health