Overview
Real World Evidence Coordinator – Location: Maidenhead (hybrid working available). Duration: 6 months initial (Temporary). Rate: up to £18 per hour (PAYE or Umbrella).
Responsibilities
* Serve as a subject matter expert for investigator-initiated study setup processes.
* Provide input into feasibility and management of clinical research involving Investigational Medicinal Products.
* Collaborate with global and local teams to monitor study progress and ensure timely drug supply delivery.
* Manage eTMF record keeping and maintain Trial Master File for essential study documents.
* Track milestones and maintain accurate records of investigational drug shipments.
* Ensure compliance with country regulations, GCP, ICH Guidelines, and company SOPs.
* Support audit and inspection readiness and participate in pre-audit activities.
* Manage budgets, invoices, and financial records for affiliate research studies.
* Prepare and execute study contracts and statements of work.
* Utilize feedback to improve processes, systems, and solutions.
Skills/Experience Required
* Life Sciences Degree (e.g. Pharmacy) or equivalent experience.
* Experience in a similar role within pharmaceutical or clinical research.
* Knowledge of ICH/GCP Guidelines and applicable local regulations.
* Extensive experience in Trial Master File record keeping and investigational drug shipment coordination.
* Experience in managing contracts and finance is desirable.
* Strong planning and organisational skills with ability to manage multiple projects.
* Proactive and positive team player with strong attention to detail.
* Fluency in English and local language (if not English).
* Proficiency in standard IT office tools and advanced Excel skills.
* Experience in audits and inspections.
To Apply
If you are interested and want
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