Clinical Research Coordinator Job at IQVIA, UK | Life Sciences | Apply Now
Are you looking to make a targeted, high-impact contribution to clinical development without committing to a long-term contract? IQVIA is currently seeking an adaptable professional for a short-term Clinical Research Coordinator Job based in West London. This 3-month assignment is an excellent way to add a premium name to your resume, gain specialized experience, and open the doors to a long-term IQVIA Career. If you are a healthcare professional or researcher seeking a flexible, part-time Life Sciences Job, this specialized site deployment offers the perfect balance of clinical execution and administrative precision.
- Job Position: Clinical Research Coordinator – London
- Location: London, United Kingdom
- Job ID: R1545300
About the Company
IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence. By building “intelligent connections” across the life sciences ecosystem, IQVIA accelerates the development of innovative medical treatments to improve patient outcomes worldwide. Taking on a role here means joining a world-class team that values integrity, rigorous data standards, and patient-centric care.
Clinical Research Coordinator Job – Key Responsibilities
As a Clinical Research Coordinator, you will serve as the operational linchpin for a specific, short-term study at a site in Hounslow. Working under the direction of the Principal Investigator, you will bridge the gap between patient care and clinical data integrity.
- Patient Advocacy & Safety: Safeguard the well-being of all study participants, act as a proactive patient advocate, and address participant concerns to ensure an ethical study environment.
- Trial Documentation: Maintain meticulous, up-to-date study records, including protocols, case report forms (CRFs), and Electronic Data Capture (EDC) systems.
- Clinical Setup & Logistics: Plan and coordinate logistical activities for study procedures. Your hands-on duties will include labeling specimen collection tubes, managing inventory, and troubleshooting specialized study equipment.
- Data Integrity Operations: Assist with data entry, execute quality control checks, and resolve data queries swiftly to ensure strict protocol compliance.
- Enrollment Support: Support active study enrollment by recruiting, screening, and orienting new participants according to protocol criteria.
- Medical Custody & Vitals: Ensure the correct handling and custody of study medications per site SOPs, and perform and document patient vital signs accurately.
- Monitor Liaison: Coordinate directly with study monitors on trial-related issues and respond effectively to monitor-initiated queries.
Qualifications & Skills Required For Clinical Research Coordinator Job
This Life Sciences Job is ideally suited for an experienced Research Nurse or a highly seasoned coordinator who can hit the ground running with minimal oversight.
- Educational Foundation: A BS/BA degree in life sciences, or an equivalent combination of education and clinical work experience.
- Professional Background: Prior experience in a clinical or medical setting as a Clinical Research Coordinator, Research Nurse, or Medical Assistant is required.
- Therapeutic Assets: Previous experience monitoring or coordinating pediatric and/or ophthalmology clinical trials is highly preferred, though not strictly mandatory.
- Technical Proficiency: Strong IT skills, with high proficiency in MS Windows and Microsoft Office applications (including Word, Excel, Outlook, and Access).
- Regulatory Knowledge: Deep foundational knowledge of clinical trials, including standard consenting processes, study schedules, and protocol-specific operating procedures.
- Interpersonal Strength: Exceptional communication skills with a natural ability to build rapid, effective working relationships with site colleagues, clinical managers, and study clients.
In summary, this short-term position is a highly strategic gateway for clinical professionals in the UK. By stepping into this Clinical Research Coordinator Job, you gain direct exposure to IQVIA’s elite data management systems and site coordination methodologies. If you possess a life sciences background, close attention to detail, and the clinical agility to support a fast-moving protocol in West London, apply today to elevate your profile and kickstart a rewarding IQVIA Career.
