Clinical Research Associate, South West England

IQVIA LLC; Bath; On-site; GBP 35,000 - 50,000; Full time

Benefits offered by this job

Career development opportunities

Mentorship across organisation

Flexible working

Well-being support

Job summary

IQVIA UK is seeking experienced Clinical Research Associates for on-site monitoring in South West England, including Bath. The role requires independent monitoring of interventional studies, ensuring GCP/ICH compliance and active collaboration with study sites.

Applicants should have at least 2 years of on-site monitoring experience and a relevant degree. The position supports career development and flexible working arrangements within the UK. Full UK right to work is required.

Qualifications

• Requires at least 2 years independent 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., GCP and ICH guidelines.
• Full UK right to work required, this position is not eligible for visa sponsorship.

Responsibilities

• Perform site monitoring visits in accordance with GCP/ICH guidelines.
• Drive subject recruitment planning and maintain regular communication with sites.
• Manage progress of studies: regulatory submissions, recruitment, CRF completion, data queries.
• Ensure TMF/ISF documents are filed and maintained per regulatory requirements.

Skills

On-site monitoring

GCP/ICH knowledge

Regulatory compliance

Communication skills

Education

Degree in scientific discipline/health care

Job description

Why IQVIA?

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 South West England.

Career development opportunities to grow as we growAI-powered career advancement through our internal talent marketplace, Career ConnectionsMentorship opportunities across the organisation via Employee Resource GroupsFlexible working to assist work-life balance and professional successWell-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) guidelinesWork with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictabilityAdminister protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issuesEvaluate 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 appropriateManage 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 phaseEnsure 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 requirementsCreate
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 documentationCollaborate and liaise with study team members for project execution support as appropriate

Requirements

Requires at least 2 years independent on-site monitoring experience of interventional studiesExperience across start-up, enrolment, maintenance, close-out Digital literacy, including confidence using AI tools in a professional settingDegree in scientific discipline / health care or equivalent industry experienceGood knowledge of, and skill in applying, applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelinesAbility to establish and maintain effective working relationships with coworkers and clientsFull 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. Learn more at IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

SummaryLocation: Bath