Clinical Trial Administrator
2 weeks ago
Senior/Clinical Trial Administrator The Senior Clinical Trial Administrator will provide daily operational and administrative support to Project Managers, Project Directors, and cross‑functional study teams. This role focuses on ensuring the completeness, quality, and inspection‑readiness of the Trial Master File (TMF/eTMF). The position also supports the Project Support function in setting up and archiving electronic TMFs. This position is a 3‑month contract that will turn into a permanent position. Hybrid Working The role requires 1–2 days a week in the office initially to integrate with the team. Key Responsibilities Administrative Support: Assist clinical project teams throughout study planning, initiation, execution, and close‑out, following ICH‑GCP, internal procedures, and regulatory standards. TMF Oversight: Maintain, update, and quality‑check TMF/eTMF content to ensure continuous inspection readiness. CTMS Management: Handle data entry, updates, and reporting within the Clinical Trial Management System. Document Tracking: Monitor study documents, essential correspondence, and contractual records. Study Materials: Prepare and review site documentation, trackers, and meeting minutes. Training Coordination: Manage study‑specific training assignments in the Learning Management System. Audit/Inspection Support: Assist with document retrieval, QC checks, and audit preparation. Team Support: Offer guidance to junior administrative staff or CTAs as needed. Qualifications Required Relevant professional experience or secondary‑level education (equivalent to high school). Fluent written and spoken English. Preferred Degree in a life‑science field or equivalent. Clinical research qualification. Experience & Technical Skills 2+ years’ administrative experience or equivalent training. At least 2 years working in clinical research. Solid understanding of GCP (E6 R3). Knowledge of clinical trial documentation standards. Experience with clinical trial management systems (CTMS/eTMF). Basic understanding of the clinical trial lifecycle. Proficient with MS Office (Word, Excel, PowerPoint, Outlook). #J-18808-Ljbffr
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Clinical Trial Administrator
2 weeks ago
Reading, United Kingdom BioTalent Full timeRecruitment Consultant - Account Management EU Contract Role Overview: The Senior Clinical Trial Administrator will provide daily operational and administrative support to Project Managers, Project Directors, and cross‑functional study teams. This role focuses on ensuring the completeness, quality, and inspection‑readiness of the Trial Master File...
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Reading, United Kingdom BioTalent Ltd Full timeA leading clinical research firm in the UK seeks a Senior Clinical Trial Administrator to provide operational and administrative support for clinical projects. This role ensures the quality and readiness of trial documents and involves hybrid working. Requirements include administrative experience, fluency in English, and a strong understanding of clinical...
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Clinical Trials Assistant
1 week ago
Reading, United Kingdom IQVIA Full timeJob Overview Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. Essential Functions - Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical...
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Sr. Clinical Trial Assistant
1 week ago
Reading, United Kingdom IQVIA Full timeInternal Job Description - IQVIA are seeking a Clinical Trial Assistant to join us on our mission to drive healthcare forward. **Hybrid working available from either Luton or High Wycombe offices (2-3 days per week), depending on your location and business needs.** A fully remote contract may be considered for specific projects. - Sr. Clinical Trial...
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Clinical Trial Assistant
1 week ago
Reading, United Kingdom Novasyte Full timeDo you want to grow your career with the World’s largest CRO? We offer genuine career progression (named on LinkedIn’s "Top Companies: The 25 best workplaces to grow your career in the UK"), supportive leadership, team spirit, a broad learning experience and impactful work. Job Overview Perform daily administrative activities, in conjunction with the...
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Clinical Trial Assistant
1 week ago
Reading, United Kingdom Novasyte Full timeExternal Job Description - Do you want to grow your career with the World’s largest CRO?- - We offer genuine career progression (named on LinkedIn’s "Top Companies: The 25 best workplaces to grow your career in the UK"), supportive leadership, team spirit, a broad learning experience and impactful work.- Job Overview - Perform daily administrative...
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Clinical Trial Lead
5 hours ago
Reading, United Kingdom IQVIA Full timeThe IQVIA Clinical Functional Service Partnerships (Clinical FSP) department is providing highly skilled professionals to our client’s project team to set-up and execute clinical trials.Joining the sponsor-dedicated team provides the opportunity to work with early phase clinical research projects (phase I and II) in different therapeutic areas. As Clinical...
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Clinical Trial Lead
6 days ago
Reading, United Kingdom IQVIA Full timeIQVIA Clinical Functional Service Partnerships (Clinical FSP) department is providing highly skilled professionals to our client’s project team to set-up and execute clinical trials. Joining the sponsor-dedicated team provides the opportunity to work with early phase clinical research projects (phase I and II) in different therapeutic areas. As Clinical...
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Clinical Trial Lead
5 days ago
Reading, Reading, United Kingdom IQVIA Full time £60,000 - £100,000 per yearThe IQVIA Clinical Functional Service Partnerships (Clinical FSP) department is providing highly skilled professionals to our client's project team to set-up and execute clinical trials. Joining the sponsor-dedicated team provides the opportunity to work with early phase clinical research projects (phase I and II) in different therapeutic areas. As...
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Clinical Trial Lead
2 weeks ago
Reading, Reading, United Kingdom IQVIA Full time £60,000 - £120,000 per yearThe IQVIA Clinical Functional Service Partnerships (Clinical FSP) department is providing highly skilled professionals to our client's project team to set-up and execute clinical trials. Joining the sponsor-dedicated team provides the opportunity to work with early phase clinical research projects (phase I and II) in different therapeutic areas. As...
