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Global Study Manager

Cambridgeshire   •  Contract/Temporary, Full time


CK Group are recruiting for a Global 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 role is working from home initially and then on site 3-4 days per week.

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 Global Study Manager role will be based at our clients site in Saffron Walden.

Salary:
£400 per day LTD.

Global Study Manager Role:

  • Perform study management tasks as per agreed delegation/oversight.
  • In partnership with internal experts and external service providers, provide oversight to ensure study delivery of both internally-run and outsourced studies.
  • Lead/contribute to the preparation of delegated study documents (e.g. Informed Consent Form, applicable study plans, etc.), and external service provider-related documents (e.g. specifications, study specific procedures, etc.).
  • Maintain and facilitate interactions with both internal & external functions to ensure efficient study delivery to time, costs and quality objectives.
  • Manage the set-up and maintenance of third-party vendors.
  • Support with budget management. Initiate contract/budget requests for third-party vendors, facilitate generation of purchase orders, track spend against approved budget and manage the change order process.

Your Background:

  • University degree (or equivalent) in medical or biological science or discipline with clinical research.
  • Relevant pharmaceutical industry and/or clinical trial experience.
  • Deep understanding of ICH-GCP, relevant regulatory/ethics requirements and clinical/drug development.
  • Proven organisational and time management skills as well as excellent attention to detail.
  • Demonstrated ability to work well both on a cross functional team and independently.
  • Experience in all phases of a clinical study lifecycle.

Apply:
Quote job ref 50202.

It is essential that applicants hold entitlement to work in the UK.


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

  • Agency: CK Group
  • Contact: Julie Marshall
  • Phone: 01438 723 500
  • Reference: 50202
  • Updated: 24th March 2021
  • Expires: 21st April 2021

CK Group

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