Position: Associate Clinical Project Manager
Location: Slough - Hybrid/On-site
Client: Biotechnology
Type: Full-time Contract
Main Responsibilities
* Support the planning, execution, and close-out of clinical trials within timelines and budget
* Coordinate cross-functional teams including clinical operations, data management, regulatory, and external vendors
* Track study milestones, deliverables, and key performance indicators
* Maintain and organize essential study documentation (e.g., TMF) in compliance with GCP and regulatory standards
* Assist in vendor selection, oversight, and performance management
* Monitor study progress and proactively identify risks or delays, escalating when needed
* Facilitate communication between internal stakeholders, clinical sites, and partners
* Contribute to study reports, project updates, and meeting materials
Main Requirements
* Bachelor’s degree in life sciences, healthcare, or a related field (advanced degree a plus)
* Previous experience in clinical research, project coordination, or clinical operations
* Understanding of clinical trial processes, ICH-GCP guidelines, and regulatory requirements
* Strong organizational and time management skills with attention to detail
* Effective written and verbal communication skills
* Ability to manage multiple tasks and work in a fast-paced environment
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