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Date Added: Thu 17/03/2022


London, UK
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Job Type: Permanent, FullTime


  • London, UK
  • Permanent
  • Salary: up to 50,000 depending on experience
  • Office and homebase opportunity

Job Description

Come and work with a global midsized CRO who have a proven track record of offering outstanding training and development for all levels of experience. From its ongoing support for their employees, they have a 90% success rate of experts who they continuously collaborate with in order to discover new solutions within the clinical research industry. This exciting new opportunity requires a passionate and driven CRA to help support multiple studies alongside its global team of likeminded professionals.

Job responsibilities

  • Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol.
  • Communication with the medical site staff including coordinators, clinical research physicians, and their site staff.
  • Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff.
  • Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP, and applicable regulatory requirements.
  • On-site and virtual/remote monitoring activities with a risk-based monitoring approach (including centralized data review) through our integrated Clinical Trial Management System to identify site deviations/deficiencies and corrective/preventive actions to bring a site back into compliance and mitigate risks moving forward.
  • Verification that the investigator is enrolling only eligible subjects.
  • Medical device and/or investigational product/drug accountability and inventory.
  • Verification and review of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol.
  • Assess the clinical research site’s patient recruitment and retention success and offering suggestions for improvement.
  • Completion of monitoring reports and follow-up letters, which includes providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure compliance.

Job qualifications

  • Must have a minimum of a bachelor’s degree in a health or science related field; Prefer Advanced Degrees or Prior clinical research experience.
  • Ability to travel 60-70% to locations nationwide is required, or less if remote/virtual visits required.
  • Must maintain a valid driver’s license and the ability to drive to monitoring sites.
  • Minimum 1 year healthcare-related work experience preferred.
  • Proficient knowledge of Microsoft® Office.
  • Strong communication and presentation skills.
  • Must be detail-oriented and efficient in time management.
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