Clinical Research Associate Job at IQVIA, UK | Life Sciences | Apply Now
If you are an experienced clinical research professional specializing in oncology, this field-based position with IQVIA’s Site Management (multi-sponsor) team is an outstanding opportunity. Located across the United Kingdom with a primary base in Oxfordshire (and additional locations available), this role allows you to directly impact the predictability, quality, and progress of life-saving oncology trials. For dedicated monitors seeking a highly rewarding Job in UK, this role offers the chance to forge a career with greater purpose. Here is a complete, scannable breakdown of this Clinical Research Associate Job, your core responsibilities, and the qualifications required to advance your IQVIA Career.
- Job Position: Clinical Research Associate
- Locations: Oxfordshire, Reading, Brighton, Chesterfield, Manchester, Nottingham, United Kingdom
- Jov ID: R1514135
About The Company
IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. Driven by a mission to help create a healthier world, IQVIA creates intelligent connections to accelerate the development and commercialization of innovative medical treatments. By joining the Site Management team, you will be part of a vast network of highly skilled professionals dedicated to improving patient outcomes and population health worldwide while continually learning and making a tangible impact.
Clinical Research Associate Job – Key Responsibilities
As a Clinical Research Associate, you will serve as the primary link between the sponsor and the clinical trial sites, ensuring that oncology studies are executed safely, ethically, and efficiently.
Your day-to-day field and operational duties will include:
- Site Monitoring Lifecycle: Performing comprehensive site monitoring visits (including selection, initiation, routine monitoring, and close-out) in strict accordance with contracted scopes of work and Good Clinical Practice (GCP).
- Patient Recruitment: Working closely with clinical sites to adapt, drive, and track subject recruitment plans in line with project needs to enhance trial predictability.
- Training & Communication: Administering protocol and study-related training to assigned sites while establishing regular lines of communication to manage ongoing expectations and troubleshoot issues.
- Quality Assurance: Evaluating the quality and integrity of study site practices, ensuring proper protocol conduct and regulatory adherence, and escalating quality issues when appropriate.
- Trial Progress Management: Tracking regulatory submissions and approvals, recruitment, Case Report Form (CRF) completion, and data query generation and resolution (may also support the start-up phase).
- Document Compliance: Ensuring required site documents are available for filing in the Trial Master File (TMF) and verifying that the Investigator’s Site File (ISF) is maintained to GCP and local standards.
- Reporting: Creating and maintaining appropriate documentation regarding site management, monitoring visit findings, and action plans by submitting regular visit reports and follow-up letters.
Qualifications & Skills Required For Clinical Research Associate Job
- This field-based role is tailored for seasoned trial monitors with a specific background in complex oncology studies.
- Educational Foundation: A degree in Life Sciences or an equivalent combination of industry experience and education is required.
- Specialized Experience: Proven experience performing independent, on-site monitoring of Oncology therapeutic area studies (specifically for unblinded studies).
- Regulatory Expertise: In-depth, functional knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
- Logistical Flexibility: A strong willingness and flexibility to travel frequently to clinical sites across the UK as required by project demands.
- Work Authorization: (Important Note: This role is not eligible for visa sponsorship; candidates must have the existing right to work in the UK).
In summary, this field-based Clinical Research Associate role at IQVIA is an exceptional opportunity for oncology-focused trial monitors wanting to maximize their impact on global health. By securing this Clinical Research Associate Job, you will leverage your GCP expertise to ensure the integrity of cutting-edge cancer therapeutics. If you possess the required independent monitoring experience and are ready to travel across sites, apply today to secure this premier Job in UK and take a significant step forward in your IQVIA Career.
