Job Description
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
ABOUT PLANET PHARMA
Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London. We have invested significantly in creating a robust international platform that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent / direct hire recruitment offering.
Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognised by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing.
We are an equal opportunities Recruitment Business and Agency.
We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age.
* www.planet-pharma.com