Clinical Research Associate Job at IQVIA, UK | Life Sciences | Apply Now
If you are an experienced clinical monitor with a specialized background in oncology and unblinded protocol management, this full-time position at IQVIA is an exceptional opportunity. Strategically aligned with IQVIA’s Site Management (multi-sponsor) division, this field-based role places you at the forefront of advanced cancer research across the United Kingdom. For clinical trial professionals searching for a high-impact Clinical Research Associate Job, this position offers end-to-end monitoring ownership of complex oncology trials, data integrity oversight, and patient recruitment strategy management. It serves as an elite operational milestone for a long-term IQVIA career and stands out as a premier choices for anyone tracking a competitive, field-based Life Sciences Job within Europe’s clinical development sector.
- Job Position: Clinical Research Associate
- Location: Chesterfield, United Kingdom
- Additional Locations: Reading, Brighton, Manchester, Nottingham, Oxfordshire, United Kingdom
- Job 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 accelerate the development and commercialization of innovative medical treatments, IQVIA connects human science with advanced technology to improve patient outcomes and population health worldwide. This specific role sits within IQVIA’s Site Management (multi-sponsor) team. Operating under this flexible architecture, you are not isolated within a single company’s portfolio; instead, you manage studies from multiple pharmaceutical and biotech sponsors concurrently. This model allows you to gain deep exposure to diverse protocols, innovative oncology compounds, and various electronic systems, all while backed by the comprehensive training platforms and career progression of the world’s largest Contract Research Organization (CRO).
Clinical Research Associate Job – Key Responsibilities
The field-based Clinical Research Associate will support high-priority Oncology studies, serving as the primary technical point of contact between regional UK investigational clinics and global study teams.
Your core field monitoring, safety, and document control duties will include:
- Full-Lifecycle Field Monitoring: Conducting all essential site visit types—including Selection (SQV), Initiation (SIV), Routine Interim Monitoring (IMV), and Close-Out Visits (COV)—in strict compliance with contracted scopes of work and Good Clinical Practice (GCP).
- Oncology Data & Unblinded Auditing: Evaluating the quality, safety, and integrity of study site practices, with a specific focus on auditing complex oncology data streams and handling unblinded study logistics to advance this Clinical Research Associate Job.
- Subject Recruitment Strategy: Partnering with site staff to adapt, drive, and track localized patient recruitment and enrollment plans, enhancing study predictability and meeting project timelines.
- Protocol & Study Training: Administering protocol-specific training to principal investigators and site coordinators, establishing regular lines of communication to manage project expectations.
- Metrics & Query Management: Tracking regulatory submissions, ethics approvals, case report form (CRF) completion, and driving the rapid generation and resolution of clinical data queries.
- TMF & ISF Governance: Verifying that all original regulatory documents are secured for filing within the central Trial Master File (TMF) while ensuring the Investigator’s Site File (ISF) is meticulously maintained.
- Reporting & Action Plans: Creating detailed site management documentation, submitting regular monitoring visit reports, and issuing precise follow-up letters to site leads for this Life Sciences Job.
Qualifications & Profile Requirements For Clinical Research Associate Job
This field position is meticulously tailored for autonomous, detail-oriented clinical professionals who can independently manage relationships with busy medical consultants and research nurses.
- Proven Oncology Background: Direct, practical experience with independent on-site monitoring of Oncology therapeutic area protocols is required.
- Unblinded Study Exposure: Hands-on experience managing the specific operational and data workflows required for unblinded clinical trials.
- Educational Foundation: A formal Bachelor’s degree in a life science discipline or related field, or equivalent industry clinical experience to accelerate an IQVIA career.
- Regulatory Grounding: In-depth, functional knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
- Mobility & Transit: High flexibility and willingness to travel regionally to investigator sites as required by the multi-center protocols.
- Legal Authorization: Applicants must possess full, permanent authorization to work in the United Kingdom. Please note: This role is explicitly not eligible for visa sponsorship.
In short, the Clinical Research Associate position within IQVIA’s multi-sponsor team is a definitive route to translating your oncology monitoring skills into a highly respected global operations asset. Securing this appointment allows you to bypass transactional administrative roles and take direct field command of the site relationships, unblinded auditing mechanics, and eTMF workflows that drive breakthrough cancer therapies to market. If you reside in the United Kingdom near a major transit hub, meet the oncology monitoring criteria, and possess an uncompromising commitment to data integrity, apply today to secure this premier Clinical Research Associate Job, launch a highly rewarding IQVIA career, and lock in this outstanding Life Sciences Job.
