Clinical Research Associate

4 weeks ago

London, Greater London, United Kingdom Life Sciences Recruitment Full time
Clinical Research Associate Job Description

We are seeking a highly skilled Clinical Research Associate to support the planning, execution, and reporting of clinical trials. As a key member of our team, you will collaborate with internal and external stakeholders to ensure the success of our clinical trials.

Key Responsibilities:
  • Assist in planning and executing clinical trials, ensuring adherence to timelines, budgets, SOPs, GCP, and regulations.
  • Conduct site recruitment and feasibility studies, collect and review essential documents, and develop study plans.
  • Maintain and close out in-house site management activities, ensuring compliance with protocols and SOPs.
  • Review and approve monitoring reports, and occasionally conduct co-monitoring visits.
  • Prepare and finalize investigator contracts, budgets, and payments.
  • Obtain, review, and process regulatory documents and informed consent forms.
Qualifications:
  • Bachelor's degree preferred.
  • 5+ years of experience in clinical trials.
  • Proficiency in English.
  • Experience in all stages of clinical trial conduct and understanding of clinical trial processes.
  • Preferred experience in managing and monitoring CROs and investigative sites.
  • Knowledge of patient recruitment, non-compliance, safety, document management, and investigational product accountability.
  • Knowledge of ICH GCP, IRB/IEC, and local regulatory authority regulations.
  • Preferred experience with bio-samples and relevant therapeutic areas.
  • Willingness to travel up to 35%.

We are a global life science recruitment firm specializing in partnering with start-ups, fast-growing biotech and pharmaceutical organizations. If you are passionate about clinical research and have the skills and experience we are looking for, please contact us to learn more about this exciting opportunity.

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