Experienced CRA — Flexible, Development-Focused & Impactful

IQVIA; United Kingdom; On-site; GBP 30,000 - 45,000; Full time

Job summary

A leading clinical research company is seeking experienced Clinical Research Associates to join its team in the UK. This role involves managing site activities for clinical trials, ensuring compliance with Good Clinical Practice, and providing training. Ideal candidates will have experience in monitoring and managing multiple trial protocols, along with a degree in life sciences. The position offers opportunities for professional development while contributing to impactful healthcare solutions.

Qualifications

• Experience of independent on-site monitoring.
• Successfully managed multiple clinical trial protocols.
• In-depth knowledge of GCP and ICH guidelines.
• Flexibility to travel to sites.

Responsibilities

• Conduct all aspects of site management and monitoring activities.
• Work with sites to adapt and track recruitment plans.
• Create and maintain monitoring visit reports and action plans.
• Co-monitor, train and mentor junior team members.

Skills

Independent on-site monitoring

Management of clinical trial protocols

Knowledge of Good Clinical Practice (GCP)

Knowledge of ICH guidelines

Flexibility to travel

Education

Life science degree or equivalent industry experience

Job description

A leading clinical research company is seeking experienced Clinical Research Associates to join its team in the UK. This role involves managing site activities for clinical trials, ensuring compliance with Good Clinical Practice, and providing training. Ideal candidates will have experience in monitoring and managing multiple trial protocols, along with a degree in life sciences. The position offers opportunities for professional development while contributing to impactful healthcare solutions.