Clinical Research Job at IQVIA, UK | Life Sciences | Apply Online
If you are an experienced clinical trials coordinator, a research nurse, or a site manager looking to apply your study-coordination and patient-screening skills within a premier global clinical research network, this part-time opportunity at IQVIA is an exceptional choice. Located at a specialized clinical research site in York, United Kingdom, this position places you on the frontline of trial delivery, patient education, and data integrity. For detail-oriented site operations specialists searching for a high-impact Clinical Research Job, this position offers hands-on mastery over Electronic Data Capture (EDC) systems, patient screening mechanics, and biofluid laboratory sample processing. It serves as an elite launchpad to expand a long-term IQVIA Career and stands out as a premier selection for professionals tracking a competitive Life Sciences Job with a highly flexible, part-time schedule.
- Job Position: Clinical Research Coordinator – York
- Location: York, United Kingdom
- Job ID: R1555193
About The Company
IQVIA is a world-renowned human data science powerhouse and the leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences industry. Operating across more than 100 countries, IQVIA creates intelligent connections across data, advanced technology, and human science to accelerate the development and commercialization of innovative medical treatments that improve patient outcomes worldwide. This position operates within IQVIA’s dedicated Site Solutions network, embedded directly at a high-volume clinical research site in York, North Yorkshire. Joining this clinical team means stepping into a supportive, fast-paced environment where your daily coordination and patient interactions translate complex trial protocols into safe, compliant, and actionable medical milestones.
Clinical Research Job – Key Responsibilities
The Clinical Research Coordinator functions as a vital operational anchor at the trial site, taking responsibility for daily administrative, clinical data, and patient-facing workflows under general supervision.
Your core screening, data entry, and lab support duties include:
- Patient Prescreening & Triage: Auditing internal electronic charts and site databases to identify, prescreen, and match eligible patient profiles for active study enrollment.
- Enrollment & Consent Oversight: Supporting active patient screening and recruitment pipelines, including handling informed consent processes and privacy documentation in accordance with protocol metrics.
- EDC System Curation: Maintaining and meticulously updating master study documentation, Case Report Forms (CRFs), and Electronic Data Capture (EDC) systems to advance this Clinical Research Job.
- Bio-Sample Processing: Handling, spinning, and processing laboratory samples and biological specimens in strict compliance with safety guidelines and study shipping protocols.
- Data Verification & Query Resolution: Executing rapid data entry, performing routine quality checks, and resolving data queries to ensure complete data accuracy and audit readiness for an optimized IQVIA Career track.
- Patient & Monitor Liaison: Delivering structured patient education regarding study schedules, while serving as a primary point of contact for external study monitors responding to site inquiries.
- General Site Administration: Coordinating multi-track logistical activities for medical procedures, managing investigator site files, and executing day-to-day administrative tasks.
Qualifications & Profile Requirements For Clinical Research Job
IQVIA seeks a highly organized, communicative clinical researcher who demonstrates a deep baseline understanding of trial site dynamics and an compromise-free approach to data precision.
- Required Experience & Academic Benchmarks:
- Site Track Record: A minimum of 2 years of active experience working as a Clinical Research Assistant, Research Nurse, or Clinical Research Coordinator directly at a clinical trial site is mandatory.
- Educational Foundation: A formal Bachelor’s degree in the Life Sciences or a closely related natural scientific discipline is considered for this Life Sciences job.
- Core Technical & Linguistic Skills:
- Solid, practical understanding of clinical trials, including extensive familiarity with study protocols, informed consent forms, patient schedules, and medical terminology.
- Strong digital workspace skills, including high proficiency in MS Office applications (Word, Excel, Outlook, Access) and clinical data logging portals.
- Excellent interpersonal communication traits, with complete fluency in written and spoken English to manage patient education and monitor audits.
- Sponsorship Notice: Applicants must possess independent, permanent working rights in the United Kingdom; sponsorship cannot be offered for this position.
In short, the Clinical Research Coordinator position at IQVIA is a definitive route to translating your site monitoring or research nursing background into a highly valuable asset with a global industry leader. Securing an appointment here allows you to move past repetitive paperwork loops and take direct operational charge of the patient screenings, EDC systems, and lab processing steps that drive international clinical development forward safely. If you reside in or can commute to York, meet the mandatory 2-year trial site baseline, and seek a high-impact part-time role, apply today to secure this premier Clinical Research Job, launch an exceptional IQVIA Career, and lock in this outstanding Life Sciences Job.
