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Clinical Project Management Associate

CK Group- Science, Clinical and Technical
Posted 8 hours ago, valid for 4 days
Location

Cambridge, Cambridgeshire CB21NT, England

Salary

£75,000 - £90,000 per annum

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Contract type

Full Time

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Sonic Summary

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  • CK Group is partnering with Nxera Pharma UK Limited to recruit a Clinical Project Management Associate for a hybrid role based in Cambridge or London.
  • The position requires proven clinical operations experience in a biopharmaceutical company, with a preference for candidates who have held a CTA or CRA position.
  • Key responsibilities include supporting clinical project planning, vendor management, and ensuring compliance with regulatory standards.
  • Candidates should hold a relevant life science degree and have experience using project management tools.
  • The role offers an excellent day rate, although specific salary details are not provided, and applicants must be entitled to work in the UK.
CK Group are working in partnership with Nxera Pharma UK Limited (formerly Sosei Heptares), to recruit a Clinical Project Management Associate. This will be a hybrid role, office based for three days a week in Cambridge or London


COMPANY:

Nxera Pharma is a technology powered biopharma company, in pursuit of new specialty medicines to improve the lives of patients with unmet needs in Japan and globally, focused on therapeutic areas in inflammation diseases, neurology and immunology.


RESPONSIBILITIES:

As Clinical Project Management Associate you will be an integral part of the Translational Medicine team, with responsibility for delivering innovative early clinical programs and ensure a seamless path to clinical proof-of-concept for priority assets.

Key duties will include:
  • Supporting the planning, implementation and monitoring of clinical and operational projects within agreed timelines and budgets.
  • Assisting in the development and maintenance of project plans, timelines, and risk management strategies.
  • Acting as the main point of contact for biomarker and bioanalytical vendors for clinical sample management.
  • Ensuring compliance with GxP, ICH-GCP, and company SOPs.
  • Supporting the preparation and review of project documentation, reports, and presentations.
  • Providing administrative support for contract management, procurement, and vendor agreements.

QUALIFICATIONS:

As Clinical Project Management Associate you will require:
  • A relevant life science degree.
  • Proven clinical operations experience gained in a biopharmaceutical company.
  • A strong understanding of the clinical trial process, vendor management, regulatory requirements and industry standards.
  • Previous experience in a CTA or CRA position is preferred.
  • Experience of using project management tools.

BENEFITS:

Excellent day rate.


APPLY:

It is essential that applicants hold entitlement to work in the UK. Please quote job reference (Apply online only) in all correspondence.


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