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Skills: Clinical research, Site monitoring, Good Clinical Practice (GCP), ICH guidelines, Subject recruitment
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Full-time
bachelor degree
Flexible working, Well-being support, Career development opportunities
Posted 12d ago
~40 hrs/week
Responsibilities
Perform site monitoring visits to ensure compliance with GCP and ICH regulatory requirements. Manage study progress by tracking recruitment, regulatory submissions, and maintaining essential site documentation.
Requirements
Requires at least 3-5 years of on-site monitoring experience for interventional studies. Candidates must hold a degree in a scientific or healthcare discipline and possess full UK work rights.
Full job description
Join IQVIA on our mission to accelerate innovation for a healthier world!
IQVIA UK’s cFSP (sponsor-dedicated) team is growing and seeking Senior Clinical Research Associates.
Why IQVIA?
Genuine career development opportunities to grow as we grow
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 3-5 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
Apply today and forge a career with greater purpose, make an impact, and never stop learning!
#LI-ADAMTHOMPSON
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 https://jobs.iqvia.com
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.
Related keywords
Clinical Research AssociateIQVIASite MonitoringGCPICHInterventional StudiesRegulatory RequirementsSubject RecruitmentTrial Master FileInvestigator's Site FileClinical TrialsLife SciencesHealthcare IntelligenceProtocol AdherenceSite Management
IQVIA (NYSE:IQV) is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. IQVIA’s portfolio of solutions are powered by IQVIA Connected Intelligence™ to deliver actionable insights and services built on high-quality health data, Healthcare-grade AI™, advanced analytics, the latest technologies and extensive domain expertise. With approximately 88,000 employees in over 100 countries, including experts in healthcare, life sciences, data science, technology and operational excellence, IQVIA is dedicated to accelerating the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.
IQVIA is a global leader in protecting individual patient privacy. The company uses a wide variety of privacy-enhancing technologies and safeguards to protect individual privacy while generating and analyzing information on a scale that helps healthcare stakeholders identify disease patterns and correlate with the precise treatment path and therapy needed for better outcomes. IQVIA’s insights and execution capabilities help biotech, medical device and pharmaceutical companies, medical researchers, government agencies, payers and other healthcare stakeholders tap into a deeper understanding of diseases, human behaviors and scientific progress, in an effort to advance healthcare. To learn more, visit www.iqvia.com.
Offices: 2400 Ellis Rd, Durham, North Carolina 27703, US
How many Healthcare jobs are open in Reading, United Kingdom right now?
There are currently 120 open healthcare positions in Reading, United Kingdom listed on Clera. New openings are added daily as companies post roles.
Which companies are hiring for Healthcare roles in Reading, United Kingdom?
Companies currently hiring include IQVIA, Spire Healthcare Group plc, ICON plc, Baxter International Inc., Guardian Angel Carers, among others. Browse the listings above to see every active employer.
Are there remote or hybrid Healthcare jobs in Reading, United Kingdom?
Yes — 45 of the 120 open healthcare positions offer remote or hybrid work (15 remote, 30 hybrid).
How do I apply for Healthcare jobs in Reading, United Kingdom?
Each listing links directly to the employer's application page. Apply early — fresh listings get the most recruiter attention in the first two weeks.