Senior Clinical Research Associate β€” Site Monitoring

Senior Clinical Research Associate β€” Site Monitoring

Full-Time 37900 - 45000 Β£ / year (est.) No working from home possible
Meeveem Limited

At a Glance

  • Tasks: Support site monitoring and mentor junior CRAs while ensuring protocol adherence.
  • Company: Worldwide Clinical Trials, a leader in clinical research.
  • Benefits: Competitive salary, travel opportunities, and professional development.
  • Other info: Dynamic role with opportunities for growth and travel.
  • Why this job: Make a difference in healthcare by working on impactful clinical trials.
  • Qualifications: 2+ years of CRA experience and a relevant degree or RN/BSN.

The predicted salary is between 37900 - 45000 Β£ per year.

Worldwide Clinical Trials in the United Kingdom is seeking a Clinical Research Associate to support site qualification, initiation, interim monitoring, and close-out visits across therapeutic areas.

You will mentor less experienced CRAs, document findings, review data, and ensure protocol adherence with IP handling and TMF updates.

Travel required; 2+ years of CRA experience and a 4-year degree or RN/BSN preferred; strong English communication essential.

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Senior Clinical Research Associate β€” Site Monitoring employer: Meeveem Limited

Meeveem Limited is an exceptional employer that values its employees by fostering a collaborative and innovative work culture in the heart of Yorkshire. With a strong focus on professional development, employees are encouraged to grow their skills and advance their careers while enjoying competitive benefits and a supportive environment that prioritises work-life balance. Joining Meeveem means being part of a dynamic team dedicated to making a meaningful impact in the cardiovascular and endovascular sectors.

Meeveem Limited

Contact Details:

Meeveem Limited Recruitment Team

We think you need these skills to ace Senior Clinical Research Associate β€” Site Monitoring

Site Qualification
Site Initiation
Interim Monitoring
Close-Out Visits
Mentoring
Documentation Skills
Data Review