London, United Kingdom | Full time | Field-based | R1545300
Clinical Research Coordinator – London (Short-Term Assignment)
Are you looking for an opportunity in Clinical Research? Do you want to work for an industry-leading company? If so, come and join us. IQVIA is currently looking for a Clinical Research Coordinator to support a short-term clinical study.
This is a short-term study assignment (3 months), working 24 hours per week, supporting a site in Hounslow, West London.
As a pivotal member of the site team, you will be involved in a variety of clinical and administrative tasks to support investigators, ensure the smooth running of clinical trials, and assist with the collection of patient data.
Key Responsibilities
* Support clinical research studies and maintain a safe study environment in accordance with health and safety policies, under the direction and delegation of the Principal Investigator
* Safeguard the well-being of study participants, act as a patient advocate, and address participant concerns
* Maintain up-to-date study documentation, including study protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems, and other essential records
* Plan and coordinate logistical activities for study procedures in line with the study protocol
* Perform clinical study set‑up and preparation, including labeling specimen collection tubes and containers, managing inventory of required supplies, and setting up or troubleshooting study equipment
* Assist with data entry, data quality checks, and query resolution to ensure protocol compliance and data accuracy
* Support study enrollment activities, including recruiting, screening, and orienting participants according to the study protocol
* Ensure correct custody and handling of study medication in accordance with site standard operating procedures
* Coordinate with study monitors on study-related issues and respond effectively to monitor‑initiated queries
* Perform and document patient vital signs
Required Skills and Experience
* BS/BA in life sciences or equivalent education and/or relevant work experience in a clinical or medical setting (e.g., Clinical Research Coordinator, Research Nurse, Medical Assistant, or similar role)
* Ideally an experienced Research Nurse or a highly experienced Clinical Research Coordinator
* Experience in pediatric and/or ophthalmology clinical trials is preferred but not essential
* Strong knowledge of clinical trials, including departmental, protocol‑specific, and study‑specific operating procedures, consent forms, and study schedules
* Strong IT skills, with proficiency in MS Windows and Microsoft Office applications (Access, Outlook, Excel, Word)
* Excellent interpersonal skills with the ability to build and maintain effective working relationships with colleagues, managers, and clients
* Strong organizational skills with close attention to detail
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