TFS HealthScience

Senior Clinical Research Associate

TFS HealthScience

contract

Posted on:

Origin:  • 🇵🇹 Portugal

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Job Level

Senior

Tech Stack

Google Cloud PlatformTFS

About the role

  • Initiation, on-site and/or remote monitoring and close out of study sites during study conduct
  • Monitor clinical trials according to TFS and/or sponsor SOPs, GCP, ICH and applicable regulations
  • Perform monitoring activities to assess and ensure subject safety, data integrity and quality
  • Verify informed consent procedures and protocol compliance to protect study participants
  • Review CRFs and source documentation for validity and accuracy
  • Work as part of the Strategic Resourcing Solutions (SRS) team to support customer study goals

Requirements

  • Experience working with Medical Devices
  • Bachelor’s Degree, preferably in life science or nursing; or equivalent
  • >3 years of experience as CRA including relevant on-site monitoring experience
  • Knowledge of GCP and ICH guidelines and applicable regulatory regulations
  • Experience with on-site and remote monitoring of clinical trials
  • Experience reviewing CRFs (electronic or paper) and subject source documentation
  • Ability to work in a fast-paced environment with changing priorities