Clinical Research Associate

3 weeks ago


Reading, Reading, United Kingdom Pharmiweb Full time
Job Summary:

Pharmiweb is seeking an experienced Clinical Research Associate to strengthen our team. As a key member of our clinical operations team, you will be responsible for performing site monitoring visits, collaborating with sites to adapt and drive subject recruitment plans, and ensuring the quality and integrity of study site practices.

Responsibilities:
  • Perform site monitoring visits in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
  • Work with sites to adapt and drive subject recruitment plans in line with project needs to enhance predictability.
  • Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations.
  • Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution.
  • Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans.
  • Collaborate and liaise with study team members for project execution support as appropriate.


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