At a Glance
- Tasks: Conduct site monitoring visits and ensure compliance with clinical research protocols.
- Company: Join IQVIA, a leader in clinical research and healthcare innovation.
- Benefits: Flexible working, career development, and well-being support for a balanced life.
- Other info: Field-based role offering hands-on experience and opportunities to connect with diverse teams.
- Why this job: Make a real impact in healthcare while growing your career in a supportive environment.
- Qualifications: 2+ years of monitoring experience and a degree in a scientific discipline.
The predicted salary is between 40000 - 50000 £ per year.
Join IQVIA on our mission to accelerate innovation for a healthier world! IQVIA UK’s cFSP (sponsor-dedicated) team is growing and seeking experienced Clinical Research Associates in Scotland.
Why IQVIA?
- Career development opportunities to grow as we grow
- AI‑powered career advancement through our internal talent marketplace, Career Connections
- 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 2 years on-site monitoring experience of interventional studies
- Degree in scientific discipline or 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
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.
Where you'll work: Field-based. You’ll work where the action is — out in the field, directly engaging with our customers, sites or partners. Field-based roles offer the opportunity to build relationships face-to-face, gain real-world insights and make a tangible impact.
The culture in IQVIA is to be constantly looking at how we can do things better to help our customers, to bring life-changing medicines to patients and also to be a part in designing and developing and implementing these solutions. It’s a fantastic opportunity.
Culture at IQVIA is built on a shared belief: that when people are empowered with better data, smarter technology and deeper expertise, they can change what’s possible for patients. Across every team and every corner of the globe, you’ll find colleagues who genuinely care — about the mission and about each other.
Clinical Research Associate II in Livingston employer: IQVIA Argentina
At IQVIA, we pride ourselves on being an exceptional employer that fosters a collaborative and innovative work culture. Our Reading location offers a hybrid working model, allowing for flexibility while engaging in meaningful projects that impact clinical outcomes globally. We are committed to employee growth, providing ample opportunities for professional development and mentorship, making it an ideal place for those looking to advance their careers in clinical research.
