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Clinical Development Director - Rare Disease - Global

Clinical Development Director - Rare Disease - Global

  • Location

    Buckinghamshire, England

  • Sector:

    Clinical Research

  • Job type:

    Permanent

  • Salary:

    Negotiable

  • Contact:

    Toby Ferguson

  • Contact email:

    info@pharma-partners.co.uk

  • Job ref:

    BBBH22983_1621580727

  • Published:

    4 months ago

  • Expiry date:

    2021-06-20

  • Consultant:

    #

Clinical Development Director - Rare Disease - Global

A newly created opportunity to become part of a growing small-mid-sized pharmaceutical business with a global presence in multiple therapy areas. This position will focus on clinical development of rare disease indications and works on Global clinical trial programmes.

As a Director in the rare disease clinical development team, you will manage and deliver clinical development plans across Phases I-II-III, and by definition work closely with clinical project teams and regulatory colleagues in Europe and the US. Your responsibilities will include:

  • Provide high levels of medical and scientific insight for your assigned developmental rare disease indications, strategically advising and guiding operational colleagues across various clinical trial programmes
  • Manage execution of clinical trial plans and protocols globally - especially for clinical trial sites in Europe and the US
  • Work seamlessly with global teams across Regulatory, Translational Medicine, Drug Safety, Medical Affairs, and Business Development, to provide on-going medical support where needed
  • Contribute to defining and delivering medical guidance on compliance with GCP across all clinical development projects and frameworks
  • Provide additional medical and scientific support to local, regional, and global teams assessing new product/indication acquisition opportunities for rare disease products

Candidate requirements include:

  • Qualified physician
  • Significant industry experience in clinical development ideally across all phases
  • Experience in rare disease in not required, though naturally a desire to work in a niche therapy area would lend itself well to this type of role
  • Global experience is desirable
  • Some prior exposure of working directly with Regulatory teams on clinical trial projects
  • Someone who enjoys a busy and fast-paced role in a very flat team structure
  • Good experience managing multiple projects and varying challenges all in one go

To apply for this position please use the "Apply" option or feel free to send your CV directly to the Pharma-Partners team via email info@pharma-partners.co.uk