CRC Associate: Clinical Research Coordination & Safety in London

CRC Associate: Clinical Research Coordination & Safety in London

London Full-Time 30000 - 40000 Β£ / year (est.) No working from home possible
ICON

At a Glance

  • Tasks: Support clinical studies, assist with patient screenings, and coordinate study visits.
  • Company: ICON is a leader in clinical research based in Northamptonshire.
  • Benefits: Offers competitive salaries and comprehensive benefits for work-life balance.
  • Other info: Role focuses on ensuring protocol adherence and data quality.
  • Why this job: Join a team committed to high-quality work and patient safety.
  • Qualifications: Must possess a relevant degree and strong organizational skills.

The predicted salary is between 30000 - 40000 Β£ per year.

ICON is looking for a CRC Associate based in Northamptonshire. In this role, you will contribute to clinical coordination activities, ensuring protocol adherence, data quality, and patient safety.

Your responsibilities will include supporting clinical studies, assisting with patient screenings, and coordinating study visits.

To succeed, you must possess a relevant degree, organizational skills, and a commitment to high-quality work.

ICON values an inclusive workplace and offers competitive salaries along with a variety of comprehensive benefits to promote work-life balance.

CRC Associate: Clinical Research Coordination & Safety in London employer: ICON

ICON, located in Northamptonshire, is dedicated to clinical research excellence. The company promotes an inclusive workplace and offers various benefits to support employee well-being. Join a team that prioritises patient safety and high-quality standards in clinical studies.

ICON

Contact Details:

ICON Recruitment Team

We think you need these skills to ace CRC Associate: Clinical Research Coordination & Safety in London

Clinical Coordination
Protocol Adherence
Data Quality Management
Patient Safety
Patient Screening
Study Visit Coordination
Organizational Skills