Experienced Clinical Research Associate

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

Join IQVIA on Our Mission to Drive Healthcare Forward

IQVIA cFSP (sponsor-dedicated) are seeking experienced Clinical Research Associates in the UK.

Why IQVIA?

Community – Collaborate with diverse teams and contribute to meaningful work that improves lives

Development – Access tailored learning and development to grow your skills and advance your career

Flexibility – Enjoy a supportive environment that helps you balance work and life

Recognition – Be celebrated for your contributions and supported in reaching your goals

Well-being – Benefit from country-specific programs that support your health and happiness

Responsibilities

• Conduct all aspects of site management and monitoring activities across assigned clinical trial sites, including selection, initiation, routine monitoring, and close-out visits
• Work with sites to adapt, drive and track subject recruitment plan Provide protocol and study training to the assigned sites
• Create and maintain monitoring visit reports and action plans
• If appropriate, co-monitor, train and mentor junior members of the team

Requirements

• Experience of independent on-site monitoring
• You have successfully managed multiple clinical trial protocols across diverse investigative sites.
• In depth knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines Life science degree educated or equivalent industry experience
• Flexibility to travel to sites

Apply today and forge a career with greater purpose, make an impact, and never stop learning!