Experienced Clinical Research Associate job opportunity at IQVIA Holdings, Inc..

Home Jobs In United Kingdom Tag: Job Experienced Clinical Research Associate position at IQVIA Holdings, Inc.


DatePosted 6 Days Ago bot
IQVIA Holdings, Inc. Experienced Clinical Research Associate
Experience: General
Pattern: full-time
Country:
apply Apply Now
Salary:
Status:

Job

Copy Link Report
degreeAssociate
loacation Reading, Berkshire, United Kingdom, United Kingdom
loacation Reading, Berks..........United Kingdom

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 the UK. Why IQVIA? We share a passion for the work we do, and the impact it has on customers and patients We are innovative, curious, and feel empowered to explore new ideas and ways of working We collaborate to bring out the best in each other and get the most out of our different skills, perspectives, and expertise We are committed to growth, always learning, and making the most of agile career opportunities Awards IQVIA is a 2026 "Glassdoor Best Place to Work in the UK" IQVIA is recognised as #1 in its category on the 2026 Fortune® World’s Most Admired Companies™ list (for the FIFTH consecutive year!) 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 Experience of independent on-site monitoring You have successfully managed multiple clinical trial protocols across diverse investigative sites. In depth knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines Life science degree educated or equivalent industry experience Flexibility to travel to sites Please note - this role is not eligible for UK 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.

Other Ai Matches

Neueinsteiger und erfahrene Mitarbeiter im Pharma- und Apothekenaußendienst (m/w/d) - Region Bodensee Applicants are expected to have a solid experience in handling Job related tasks
Analista Sr. de Inteligência de Mercado - Rio de Janeiro/RJ Applicants are expected to have a solid experience in handling Job related tasks
Freelance- Translators/Linguists, Latvian into English Applicants are expected to have a solid experience in handling Latvian into English related tasks
Prod Supp Tech Advisor 2 Applicants are expected to have a solid experience in handling Job related tasks
Mobile LVN/LPN-Per Diem In-Home Services Applicants are expected to have a solid experience in handling Job related tasks
Pharmaberater m/w/d Adipositias Applicants are expected to have a solid experience in handling Job related tasks
Pharmaberater m/w/d Diabetes Applicants are expected to have a solid experience in handling Job related tasks
Epidemiologist, Inflammation, Real-World Evidence (FSP Sponsor-Dedicated) Applicants are expected to have a solid experience in handling Inflammation, Real-World Evidence (FSP Sponsor-Dedicated) related tasks
Intern Applicants are expected to have a solid experience in handling Job related tasks
Associate Content Design Specialist with Hebrew Applicants are expected to have a solid experience in handling Job related tasks
Freelance- Translators/Linguists, Serbian into English Applicants are expected to have a solid experience in handling Serbian into English related tasks
Sr Dir, Business Development Applicants are expected to have a solid experience in handling Business Development related tasks
Clinical Research Coordinator (Contract) Applicants are expected to have a solid experience in handling Job related tasks
Senior Medical Science Liaison Biosimilars F/H Applicants are expected to have a solid experience in handling Job related tasks
Mobile LVN/LPN-Per Diem In-Home Services Applicants are expected to have a solid experience in handling Job related tasks
Experienced Clinical Research Associate, Ukraine Applicants are expected to have a solid experience in handling Ukraine related tasks
Patient Site Engagement Manager Applicants are expected to have a solid experience in handling Job related tasks
Senior Director, BioAnalytical Applicants are expected to have a solid experience in handling BioAnalytical related tasks
MedTech - Part Time Clinical Nurse Consultant – LA South Applicants are expected to have a solid experience in handling Job related tasks
Pre-Analytical Services Associate (Specimen Processing) Applicants are expected to have a solid experience in handling Job related tasks
Pharmacy Technician – Onsite Applicants are expected to have a solid experience in handling Job related tasks
Consultant, Strategy Consulting Applicants are expected to have a solid experience in handling Strategy Consulting related tasks
Associate Clinical Project Management Director (CVRM), IQVIA Biotech Applicants are expected to have a solid experience in handling IQVIA Biotech related tasks