Senior Clinical Trial Assistant
At
IQVIA , we are seeking a highly motivated and detail-oriented Senior Clinical Trial Assistant to join our team. The successful candidate will be responsible for providing administrative support to the clinical research team, ensuring the timely completion of tasks, and maintaining accurate records. Key Responsibilities:
Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with updating and maintaining clinical documents and systems, including the Trial Master File (TMF). Collaborate with the clinical team on the preparation, handling, distribution, filing, and archiving of clinical documentation and reports. Review study files and completeness on a periodic basis. Coordinate the tracking and management of Case Report Forms (CRFs), queries, and clinical data flow. Act as a central contact for the clinical team for designated project communications, correspondence, and associated documentation. Qualifications:
Knowledge of applicable clinical research regulatory requirements, including Good Clinical Practice (GCP) and International Conference on Harmonization (ICH). Minimum 6 months of clinical research experience is strongly preferred. Proficiency in Microsoft Word, Excel, and PowerPoint. Effective written and verbal communication skills, including good command of the English language. Estimated Salary: £35,000 - £45,000 per annum This role requires a hybrid working arrangement with 3 days per week spent on-site in Luton with the sponsor, a global biopharmaceutical company. If you are a highly organized and detail-oriented individual with excellent communication skills, please submit your application.
At
IQVIA , we are seeking a highly motivated and detail-oriented Senior Clinical Trial Assistant to join our team. The successful candidate will be responsible for providing administrative support to the clinical research team, ensuring the timely completion of tasks, and maintaining accurate records. Key Responsibilities:
Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with updating and maintaining clinical documents and systems, including the Trial Master File (TMF). Collaborate with the clinical team on the preparation, handling, distribution, filing, and archiving of clinical documentation and reports. Review study files and completeness on a periodic basis. Coordinate the tracking and management of Case Report Forms (CRFs), queries, and clinical data flow. Act as a central contact for the clinical team for designated project communications, correspondence, and associated documentation. Qualifications:
Knowledge of applicable clinical research regulatory requirements, including Good Clinical Practice (GCP) and International Conference on Harmonization (ICH). Minimum 6 months of clinical research experience is strongly preferred. Proficiency in Microsoft Word, Excel, and PowerPoint. Effective written and verbal communication skills, including good command of the English language. Estimated Salary: £35,000 - £45,000 per annum This role requires a hybrid working arrangement with 3 days per week spent on-site in Luton with the sponsor, a global biopharmaceutical company. If you are a highly organized and detail-oriented individual with excellent communication skills, please submit your application.
