Clinical Trial Manager

£400 - £420 per day
  1. Interim/Contract
Uxbridge, London
  1. Clinical Operations, Monitoring
Posted: 05/12/2019
BBBH12964

This vacancy has now expired. Please see similar roles below...

Hobson Prior are currently seeking a Clinical Trial Manager for a research-based biopharmaceutical company. Our client is very patient-focused, whose scientific research has benefitted hundreds of thousands of people by ensuring medications are available to those who could otherwise not afford them. This is 12-month contract role located in Uxbridge, London.


Job Responsibilities:

  • You will manage global outsourced studies managed by an EU-based Clinical Program Manager.
  • Ensures effectiveness of site budget/contract process.
  • Maintains study timelines.
  • You will represent as the primary point of contact for CROs, addressing questions and applying knowledge to resolve problems.
  • Accountable to manage CROs/vendors.
  • Organises review of data listings and preparation of interim/final clinical study reports.
  • Conducts Monitoring/co-monitoring as required.
  • Assists in determining the activities to support a project's priorities within functional area.
  • You will support the Clinical Operations Europe Therapeutic Area Lead in their duties.
  • Contributes to Clinical Operations Europe team activities & initiatives
  • You will work with Clinical Program Managers to identify issues and adapt to changes.
  • Co-operate with cross-functional teams internally and externally to ensure trial progress.
  • Will incorporate study logistics and planning to accomplish study objectives.
  • May serve as a resource for others within the company for clinical trials management expertise.


Requirements:

  • BSc/ BA (in a relevant scientific discipline) or a RN qualification.
  • Therapeutic area (Oncology) experience would be preferred.
  • Must have solid previous study management/coordination experience.
  • Hands on experience of actively setting up and running clinical trial sites across multiple countries in Europe.
  • Must have monitoring experience as co-monitoring will be required.
  • Thorough knowledge and understanding of FDA and EU Regulations, ICH Guidelines, and GCPs governing the conduct of clinical trials is essential.
  • Additional European language would be beneficial but not essential.

Apply now:

If you are interested in learning more or applying to this exciting opportunity, please complete the form below and attach a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist, please request a call back at the top of this page.

Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.

Upload CV