At a Glance
- Tasks: Monitor clinical trials and ensure compliance with regulations while supporting innovative oncology research.
- Company: Join IQVIA, a leader in healthcare innovation and research.
- Benefits: Flexible working, well-being support, and genuine career development opportunities.
- Other info: Recognised as a top workplace with excellent growth potential.
- Why this job: Make a real impact in healthcare while advancing your career in a supportive environment.
- Qualifications: 3-5 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’s Site Management (full service / multi-sponsor) team is growing and seeking Senior Clinical Research Associates in the UK.
Why IQVIA?
- Genuine 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 CompaniesTM 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 Investigators 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 3-5 years on-site monitoring experience of interventional studies
- 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 driving license and access to vehicle for travel to sites
Please note - this position is not eligible for visa sponsorship. Apply today and forge a career with greater purpose, make an impact, and never stop learning!
Senior Clinical Research Associate, Oncology employer: IQVIA LLC
At IQVIA, we are committed to fostering a dynamic work environment that prioritises employee well-being and professional growth. As a Senior Clinical Research Associate in Manchester, you will benefit from flexible working arrangements, comprehensive support for your physical and mental health, and access to AI-driven career advancement tools. Join us and be part of a team recognised as one of the best places to work, where your contributions directly impact the future of healthcare.
