At a Glance
- Tasks: Monitor clinical trials, ensuring compliance and quality at research sites.
- Company: Join IQVIA, a leader in healthcare innovation and research.
- Benefits: Flexible working, career development, and well-being support for a balanced life.
- Other info: Recognised as a top workplace with excellent growth opportunities.
- Why this job: Make a real difference in healthcare while advancing your career.
- Qualifications: 12 months of monitoring experience and a degree in a scientific discipline.
The predicted salary is between 35000 - 45000 £ per year.
Portishead, United Kingdom | Full time | Field-based
Join IQVIA on our mission to accelerate innovation for a healthier world!
Why IQVIA?
- Career development opportunities to grow as we grow
- AI‑powered career advancement through our internal talent marketplace, Career Connections
- Mentorship opportunities across the organisation via Employee Resource Groups
- Flexible working to assist work–life balance and professional success
- Well‑being support covering your physical, mental, and financial health
Awards
- 2026 "Glassdoor Best Place to Work in the UK" #1 in category
- 2026 Fortune® World’s Most Admired Companies™ list (for the FIFTH consecutive year!)
- Brandon Hall Excellence Award for Learning & Development
Responsibilities
- Perform site monitoring visits (selection, initiation, monitoring and close‑out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
- Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability
- Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues
- Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate
- Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start‑up phase
- Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator’s Site File (ISF) is maintained in accordance with GCP and local regulatory requirements
- Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow‑up letters and other required study documentation
- Collaborate and liaise with study team members for project execution support as appropriate
Requirements
- Requires at least 12 months independent on‑site monitoring experience of interventional studies
- Experience across start‑up, enrolment, maintenance, close‑out
- Digital literacy, including confidence using AI tools in a professional setting
- Degree in scientific discipline / health care or equivalent industry experience
- Good knowledge of, and skill in applying, applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
- Ability to establish and maintain effective working relationships with coworkers and clients
- Full UK right to work required, this position is not eligible for visa sponsorship
Clinical Research Associate II, South West England employer: IQVIA Argentina
IQVIA is an exceptional employer, offering a dynamic work culture that prioritises career development and employee well-being. With flexible working arrangements, comprehensive support for physical, mental, and financial health, and recognition as one of the best places to work in the UK, employees are empowered to thrive both personally and professionally. The South West England location provides a vibrant environment for Clinical Research Associates to engage in meaningful work while enjoying a balanced lifestyle.
We think you need these skills to ace Clinical Research Associate II, South West England
Communication Skills
Problem-Solving Skills
Teamwork
Organizational Skills
Adaptability
Compassion
Flexibility
