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Manager Clinical Affairs
JR United Kingdom
Maidstone
Presencial
GBP 70.000 - 90.000
Tempo integral
Há 30+ dias

Resumo da oferta

A leading Consumer Goods firm in the UK is seeking a Senior Manager, Global Clinical Affairs to oversee medical device, OTC, and cosmetics safety and efficacy studies. The ideal candidate will have a strong background in biological sciences and at least 8 years of relevant experience. This role is crucial in ensuring compliance and driving product innovation through robust study management and cross-functional collaboration.

Qualificações

  • 8+ years of in vitro and clinical testing experience in medical devices, OTC, or cosmetics.
  • Proven ability to lead complex projects across multiple categories and geographies.
  • Knowledge of MDR – CER/BER and medical device safety/efficacy testing (preferred).

Responsabilidades

  • Lead medical device, OTC, and cosmetics safety and efficacy studies.
  • Manage full study lifecycle: protocol development, budget, monitoring, data interpretation, and reporting.
  • Collaborate cross-functionally with Regulatory, Legal, Marketing, and Quality teams.

Conhecimentos

Strategic leadership
Cross-functional collaboration
Regulatory compliance knowledge
Problem-solving
Strong communication skills

Formação académica

BS, MS, or PhD in biological sciences
Descrição da oferta de emprego

Blackfield Associates are supporting a leading Consumer Goods manufacturing organisaiton, who are seeking a strategic and hands-on Senior Manager, Global Clinical Affairs to lead medical device, OTC, and cosmetics safety and efficacy studies, including claims substantiation. This role is pivotal in designing and managing robust in vitro and clinical programs that meet regulatory requirements and drive product innovation.

What You’ll Do

  • Partner with Product Development to create innovative, scientifically sound study strategies.
  • Design and oversee safety and claims substantiation studies for diverse product categories.
  • Collaborate cross-functionally with Regulatory, Legal, Marketing, and Quality teams to deliver compliant protocols and actionable study results.
  • Build and expand internal and external networks with CROs, consultants, auditors, and investigators.
  • Manage full study lifecycle: protocol development, budget, monitoring, data interpretation, and reporting.
  • Present high-impact study results to inform timely business decisions.

What You Bring

  • BS, MS, or PhD in a biological science (e.g., Toxicology, Pharmacology, Biology, Physiology, Biochemistry).
  • 8+ years of in vitro and clinical testing experience in medical devices, OTC, or cosmetics.
  • Proven ability to lead complex projects across multiple categories and geographies.
  • Knowledge of MDR – CER/BER and medical device safety/efficacy testing (preferred).
  • Strong communication, problem-solving, and organizational skills.
  • Track record of conference presentations and peer-reviewed publications.
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* O salário de referência é obtido com base em objetivos de salário para líderes de mercado de cada segmento de setor. Serve como orientação para ajudar os utilizadores Premium na avaliação de ofertas de emprego e na negociação de salários. O salário de referência não é indicado diretamente pela empresa e pode ser significativamente superior ou inferior.

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