Clinical Project Associate - West London, United Kingdom - ISR Recruitment

ISR Recruitment
ISR Recruitment
Verified Company
West London, United Kingdom

2 weeks ago

Tom O´Connor

Posted by:

Tom O´Connor

beBee Recruiter
Description

Hybrid-working (2 days onsite, 3 days WFH):

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Stockley Park, Uxbridge:

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12 month contract:

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c£18 to £22 per hour (via PAYE/Umbrella)

The Opportunity:


To join a global pharma leader working as a Clinical Project Administrator on an initial 12 month contract providing administrative and coordination support for a number of high-profile Virology projects.


Full training will be provided on internal systems that will allow you to build knowledge and become an integral team-player, allowing you the time to learn the required skills to manage multiple stakeholders with ongoing operational support.


Skills and Experience:


To be considered for this position you will require a minimum of 12 months on-site clinical trial monitoring experience in a commercial CRO or sponsor environment, or with applicable clinical research regulatory requirements, i.e.

GCP and ICH guidelines.

  • BSc in a relevant scientific discipline preferred
  • Prior experience at CPA level would be useful but not a must
  • Knowledge of MHRA and or EU Regulations, ICH Guidelines, GCP, and/or familiarity with standard clinical operating procedures is a plus
  • Must be familiar with Word, PowerPoint and Excel
  • Excellent verbal and written communication skills and interpersonal skills are required.
  • Must be able to work both independently and as part of a team

Role and Responsibilities:


  • Provides administrative assistance in study implementation and the ongoing coordination, either directly or via CROs
  • Tracking and preparing studyspecific information utilizing databases, spreadsheets, and other tools
  • Working with the different members of the study management team as necessary to resolve study related administrative tasks
  • Printing and coding of study documentation for the Trial Mater File system (TMF), and/or upload of documents to the Veeva eTMF system
  • Completion of transmittal forms when necessary and filing of documentation into the TMF according to the client's SOPs
  • Performing detailed TMF reviews according to the client's SOPs and processes
  • Under close supervision reviews and participates in the quality assurance of data or documents
  • Any other tasks as delegated by the study team.

Applications:

**Please call Edward Liang here at ISR Recruitment on to learn more?
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