Site Management Associate I
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About the role
Hybrid Site Management Associate role based in Oxford, with two office days per week. Supports UK clinical research projects through site communication, clinical supplies coordination, audit and inspection preparation, TMF and OSF management, safety information flow, tracking systems, meeting support and administrative tasks. A College/University Degree in Life Sciences and MS Office proficiency are required; clinical research, CRO and Site Coordinator experience are preferred.
Key requirements
- • College/University Degree in Life Sciences
- • Required skills: clinical research project support, data and document exchange, clinical supplies management, administrative financial support, audit and inspection coordination, meeting organization and minute preparation, tracking system maintenance, Trial Master File (TMF) maintenance and review, Onsite Study File (OSF) management, safety information coordination, standard MS Office applications, organizational and planning skills, problem-solving, multi-tasking, teamwork, customer service and interpersonal skills
Opportunity details
- • Workplace: Hybrid
- • Posted: Oct 9, 2026
- • Original advert language: English
Full vacancy
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Job title: Site Management Associate I
Location: Oxford, England, United Kingdom