Clinical Trials Project Associate




Administration, Administrator


£17.31 Per Hour



Contract Type:


Date Posted:

15/09/2021 11:20:00

Details :

  • Full-time contract position
  • ASAP start for minimum 12 month contract
  • Flexible working 3 days from home
  • Competitive daily rate of pay
  • Global pharma company

Specific Responsibilities:

  • The position entails work under general supervision for routine tasks and with detailed instructions on new assignments.
  • Primary responsibilities include: Tracking and preparing study-specific information utilizing databases, spreadsheets, and other tools.
  • Coordinating and filing to the Trial Master File, both paper and electronic systems to ensure documents are filed and tracked in a complete and timely manner
  • Working with the different members of the study management team as necessary to resolve study related administrative issues
  • Serves as Clinical Trial Management Associate back up providing verbal and written communication with study personnel if appropriate.
  • Under close supervision reviews and participates in the quality assurance of data or documents.
  • Arranges meeting logistics.
  • Drafts meeting agendas and prepares meeting minutes.
  • Interacts with other departments, as directed, to complete assigned tasks.

Experience & Skills

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

Parkside Recruitment Ltd is acting as an Employment Business in relation to this vacancy. Parkside Recruitment is an Equal Opportunities Employer.