Freelance CRA β€” UK Field Monitoring in Oncology Trials

Freelance CRA β€” UK Field Monitoring in Oncology Trials

Freelance 29700 - 36300 Β£ / year (est.) No working from home possible
IQVIA LLC

At a Glance

  • Tasks: Monitor clinical trials and ensure study milestones are met while travelling across the UK.
  • Company: Join IQVIA, a leader in biotech and clinical research.
  • Benefits: Flexible freelance role with travel opportunities and exposure to various oncology trials.
  • Other info: Dynamic role with collaboration opportunities across Phase I–IV trials.
  • Why this job: Make a real impact in oncology while gaining valuable experience in clinical research.
  • Qualifications: At least 2 years as a CRA with oncology experience and strong communication skills.

The predicted salary is between 29700 - 36300 Β£ per year.

IQVIA has several exciting freelance CRA positions in the UK, with travel across the UK for site visits.

Start: asap.

Duration: approx. 6 months.

Responsibilities include monitoring clinical trials per GCP, coordinating with CTM/Lead CRA, and ensuring study milestones are met.

Role requires at least 2 years as a CRA, oncology experience, and strong communication skills.

Travel-heavy role offers exposure to Phase I–IV trials and collaboration with IQVIA Biotech and sponsors.

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Freelance CRA β€” UK Field Monitoring in Oncology Trials employer: IQVIA LLC

IQVIA LLC is an exceptional employer located in the vibrant town of Livingston, Scotland, offering a dynamic work culture that prioritises scientific excellence and patient outcomes. Employees benefit from comprehensive training and development opportunities, fostering personal and professional growth within the clinical lab services sector. With a strong emphasis on teamwork and innovation, IQVIA provides a rewarding environment for those looking to make a meaningful impact in healthcare.

IQVIA LLC

Contact Details:

IQVIA LLC Recruitment Team

We think you need these skills to ace Freelance CRA β€” UK Field Monitoring in Oncology Trials

Clinical Trial Monitoring
Good Clinical Practice (GCP)
Oncology Experience
Communication Skills
Project Coordination
Site Visit Management
Study Milestone Tracking