Clinical Research Assistant: Study Coordination & GCP

Clinical Research Assistant: Study Coordination & GCP

Full-Time 24300 - 29700 Β£ / year (est.) No working from home possible
Eurofins

At a Glance

  • Tasks: Support clinical studies by managing documents, tracking data, and ensuring compliance with regulations.
  • Company: Join Eurofins Alba Science Ltd., a leader in clinical research based in Edinburgh.
  • Benefits: Gain hands-on experience, develop your skills, and work in a supportive team environment.
  • Other info: Opportunity to grow your career in a dynamic and impactful field.
  • Why this job: Make a difference in healthcare while working on exciting clinical research projects.
  • Qualifications: Interest in clinical research and strong organisational skills are essential.

The predicted salary is between 24300 - 29700 Β£ per year.

Eurofins Alba Science Ltd. in Edinburgh is seeking a Clinical Research Assistant to support delivery of a portfolio of clinical studies.

You will assist with regulatory processes, document control, study tracking and data collection, ensuring adherence to GCP and study governance.

You will work with the Technical research team to manage volunteer recruitment, sample handling, and liaise with Project Managers to maintain study timelines and quality across multiple studies.

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Clinical Research Assistant: Study Coordination & GCP employer: Eurofins

Eurofins in Livingston, Scotland is an excellent employer that prioritises employee well-being and professional growth. With a supportive work culture, enhanced annual leave, a robust pension plan, and comprehensive health programs, employees are encouraged to thrive both personally and professionally. The opportunity to lead in a dynamic environment while contributing to meaningful projects makes Eurofins a rewarding place to advance your career.

Eurofins

Contact Details:

Eurofins Recruitment Team

We think you need these skills to ace Clinical Research Assistant: Study Coordination & GCP

Regulatory Processes
Document Control
Study Tracking
Data Collection
Good Clinical Practice (GCP)
Study Governance
Volunteer Recruitment