Global Pharma is recruiting for an Exp Senior Clinical Supplies Coordinator - 12-month contract hybrid (West London)

You will be responsible for investigational product cell journey logistics.
This role is a part of the study management team and reports to the Clinical Operations Logistics Manager.
• Participates with cross-functional project teams and may be assigned program management.
• Serves as primary liaison and clinical trial resource for the screening and enrolment of clinical trial participants across multiple clinical studies.
• Serves as back up liaison and clinical trial resource for the screening and enrollment of clinical studies.
• Proactively communicates with site research staff, vendors, and manufacturing to schedule and coordinate the “cell journey” activities as well as initiation/completion of study treatment and subsequent patient visits.
• Coordinates all aspects of study participant sample collection and “cell journey”
• Prepares metrics and updates for management as assigned. Proactively identifies potential study issues/risks and recommends/implements solutions.
• Works with multiple CRO's to communicate detailed timelines and ensure that performance expectations are met.
• Participates in the development, review and implementation of departmental SOPs and processes.
• Creates and manages clinical logistics programs as assigned.
Basic Qualifications: • 6+ years of relevant clinical or logistics experience • 4+ years of relevant clinical or logistics experience with a BS/BA • 2+ years of relevant clinical or logistics experience with MS/MA
Ideally, you will have
• Knowledge and/or experience with Clinical Trials, Cell Therapy specifically considered a plus
• Ability to work with multiple databases and electronic systems. Including experience with Oracle/ERP, courier, and material ordering portals,
• Attention to detail required.
• Outstanding organizational skills with the ability to multi-task and prioritize
• Excellent interpersonal, verbal and written communication skills
• Possesses knowledge of clinical trials and logistics and can assist project teams with this knowledge.
• Knowledgeable of FDA and ICH requirements as they pertain to clinical trials.
• Knowledgeable of domestic and international logistics/transport of biologic material (IATA, ICAO, ADR, DOT, WHO).
• Ability to author documents
• Ability to present at study meetings
• Ability to partner with other functions