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Associate Study Manager

Cambridgeshire CB21   •  Contract/Temporary, Full time


CK Group are recruiting for an Associate Study Manager to join a company in the Pharmaceutical industry at their site based in Saffron Walden on a contract basis for 12 months. The job is remote with some occasional travel to site.

Company:
Our client is a global pharmaceutical company with a major presence in the UK. Their purpose is to deliver life-changing medicines and to do this they are completely science-led and like to share this with the scientific, healthcare and business communities within the UK.

Location:
This Associate Study Manager role will be based at our clients site in Saffron Walden.

Salary:
Up to £500 per day LTD - outside IR25.

Associate Study Manager Role:
? Plan and manage Investigational Medicinal Product (IMP) supply for assigned clinical studies.
? Work collaboratively within Logistics and Clinical Supply (LCS) to ensure seamless delivery by LCS Matrix team (Study, Vendor, Distribution and Systems management activities).
? Liaise with interfaces and stakeholders internally and externally as required to ensure highly effective clinical supply planning and execution, including on-going responsiveness to any changes that may impact supply strategy.
? Plan and manage IMP supply for assigned clinical studies.
? The Associate Study Manager will typically be responsible for management of a number of clinical studies which may include a portfolio of External Sponsored Research studies (ESR) and may involve a few different development compounds. Studies may be domestic and /or international in scope and may be in clinical development Phase 1 or 2.

Your Background:
? BSc degree in basic or Applied Science or Engineering. You will have appropriate direct experience working in a development or technical operations environment in the pharmaceutical, scientific or health care product industry. Specific experience in IMP management and/or supply is desirable.
? Some experience in planning and managing IMP supply for clinical studies, including oversight of vendor GMP operations.
? Experience in the Biotechnology and/or Pharmaceutical industry is required and some prior experience in IMP management and supply is preferred.
? Preferably will have a working knowledge of the drug development process.
? Some prior experience and/or working understanding of cGMP, GCP and ICH guidelines as relates to IMP labelling, packaging and distribution.

Apply:
Entitlement to work in the UK is essential.  Please quote reference 50812.


You must be eligible to work in the UK. Learn more

  • Agency: CK Group
  • Contact: Julie Marshall
  • Phone: 01438 723 500
  • Reference: 50812
  • Posted: 7th September 2021
  • Expires: 5th October 2021

CK Group

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