Clinical Trial Manager

£400 - £450 per day
  1. Interim/Contract
Uxbridge, London
  1. Clinical Operations, Clinical Trial Administration
Posted: 04/08/2020
BBBH14717

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

Hobson Prior are currently seeking a Clinical Trial Manager for an exciting position at 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 position will be based in Stockley Park with 2 days working from home.

Job Responsibilities:

  • You will work with Clinical Program Managers to manage the European component of global clinical trials and/or the entire process of a local clinical trial, with the ability to identify issues and adapt to changes.
  • Will incorporate study logistics and planning to accomplish study objectives.
  • Co-operates with cross-functional teams internally and externally to ensure trial progress.
  • Represent as the primary point of contact for CROs, addressing questions and applying knowledge to resolve problems.
  • Any other assigned tasks.

Key Skills:

  • Must be able to generally understand, interpret, and explain protocol requirements to others.
  • Capable of prioritizing multiple tasks.
  • Must be able to participate in multiple departmental or interdepartmental strategic initiatives under limited supervision.
  • Must have a general, functional expertise to support SOP development and implementation.
  • Ability to resolve problems using national and international regulations, guidelines, and investigator interaction.
  • Excellent communication and influencing skills and ability to create a clear sense of direction is necessary.

Requirements:

  • Inflammation or rheumatology therapeutic area experience would be beneficial.
  • Must have multinational (including EU) clinical trials experience including study management/coordination.
  • Solid previous study management/coordination experience is a must.
  • Must have monitoring experience as site monitoring and/or 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.
  • International travel will be required, contingent on travel restrictions being lifted (up to approximately 20%).

Apply now:

If you are interested in learning more or applying to this exciting opportunity then please click "Apply" and upload a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist directly, please select "Contact me" 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.

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