(Senior) Clinical Trials Coordinator / Administrator, Oxford

(Senior) Clinical Trials Administrator, OxfordOxfordReference: 3012
  • Small/Mid-sized Biotech operating out of the Oxford area
  • Impressive product pipeline
  • A close knit team which is rapidly expanding over the next 12 months
  • A good time to join, with impressive funding behind them and a sound plan for the future
  • Generous salary

Are you a Clinical Trials Coordinator (or equivalent) in the Oxford area? How does working with a small and agile company with an exciting early phase pipeline sound? Our client – a well-funded and growing Biotechnology business – is looking for a Clinical professional to come into the company and manage the essential documentation for a number of their  Phase I-III studies, and control the coordination and tracking of essential trial information. This is a broad role and reports directly into the Head of Clinical Operations.

As far as company profiles go, it doesn’t get much better from the perspective of your career. Having recently completed further funding to the tune of millions, they’re rapidly expanding their clinical operations team and would be keen to hear from people matching the below requirements:

Your experience:

Essential:

  • Well versed in Clinical Trials documentation at various points of study
  • Experience of working with multiple vendors including CROs
  • Circa 5+ years’ working within the Pharma or Biotech industry in an administrative capacity or similar
  • An understanding of GCP requirements and regulatory activities
  • Good understanding of electronic clinical filing systems and documents such as the SOF and eTMF
  • A background across various stages of study lifecycles with particular attention on study start up, including the creation of the Investigator Site File (ISF)
  • Sound understanding of Microsoft Office including MS Project

Preferred:

  • Educated to degree level (ideally within Life Sciences)

The role:

  • Prepare, track and coordinate all essential clinical trial documentation
  • Maintain the Sponsor oversight files and/or the electronic Trials Master File
  • Design and compose the Investigator Site Files alongside preparing continuing study materials to Investigator Sites
  • Track a process payments including the raising of purchase orders
  • Facilitate the tracking of submissions on relevant ethics, R&D and regulatory matters
  • Support the Clinical Research staff within the department in an administrative capacity
  • Create and maintain study contact lists
  • Assist and support the tracking and management of safety documents including SUSAR reporting

The company:

  • Small/Mid-sized Biotech operating out of the Oxford area
  • Impressive product pipeline
  • A close knit team which is rapidly expanding over the next 12 months
  • A good time to join, with impressive funding behind them and a sound plan for the future

The Salary:

In order to secure the services of the right candidate our client is willing to be negotiable on salary. After an application, a consultant would be happy to include further information as to the financials in a call.

 

Zest is working to a tight deadline on this project so please press apply now and a consultant will review your details immediately.

 

Contact: Jason Cox
Email: jason.cox@zestbusinessgroup.com
Telephone: 0114 229 1672