Oncology CRA II: UK On-Site Monitoring & Multi-Study Trials in London

Oncology CRA II: UK On-Site Monitoring & Multi-Study Trials in London

London Full-Time 40000 - 50000 Β£ / year (est.) No working from home possible
Planet Pharma

At a Glance

  • Tasks: Monitor oncology trials on-site and ensure compliance with regulations.
  • Company: Planet Pharma, a dynamic leader in clinical research.
  • Benefits: Opportunities for national travel and professional growth.
  • Other info: Exciting environment with potential for career advancement.
  • Why this job: Join a team making a difference in cancer research and patient care.
  • Qualifications: Minimum 1.5 years of experience in clinical research.

The predicted salary is between 40000 - 50000 Β£ per year.

Planet Pharma is seeking a Clinical Research Associate II to work in a dynamic environment focused on oncology trials in the UK.

Responsibilities include performing on-site monitoring and ensuring compliance with ICH-GCP regulations across multiple studies.

The ideal candidate will have a minimum of 1.5 years of experience and the ability to conduct 8-10 days of monitoring each month. Opportunities for national travel and professional growth are available.

Oncology CRA II: UK On-Site Monitoring & Multi-Study Trials in London employer: Planet Pharma

At Planet Pharma, we pride ourselves on being an excellent employer, offering a vibrant work culture that fosters collaboration and innovation in the field of oncology research. Our employees benefit from extensive professional growth opportunities, including national travel and the chance to work on diverse multi-study trials, all while ensuring compliance with the highest industry standards. Join us in making a meaningful impact in clinical research, where your contributions are valued and recognised.

Planet Pharma

Contact Details:

Planet Pharma Recruitment Team

We think you need these skills to ace Oncology CRA II: UK On-Site Monitoring & Multi-Study Trials in London

On-Site Monitoring
ICH-GCP Compliance
Clinical Trial Management
Experience in Oncology Trials
Monitoring Skills
Attention to Detail
Time Management