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Position: Associate Clinical Project ManagerLocation: Slough – Hybrid/On-siteClient: BiotechnologyType: Full-time ContractMain ResponsibilitiesSupport the planning, execution, and close-out of clinical trials within timelines and budgetCoordinate cross-functional teams including clinical operations, data management, regulatory, and external vendorsTrack study milestones, deliverables, and key performance indicatorsMaintain and organize essential study documentation (e.g., TMF) in compliance with GCP and regulatory standardsAssist in vendor selection, oversight, and performance managementMonitor study progress and proactively identify risks or delays, escalating when neededFacilitate communication between internal stakeholders, clinical sites, and partnersContribute to study reports, project updates, and meeting materialsMain RequirementsBachelor’s degree in life sciences, healthcare, or a related field (advanced degree a plus)Previous experience in clinical research, project coordination, or clinical operationsUnderstanding of clinical trial processes, ICH-GCP guidelines, and regulatory requirementsStrong organizational and time management skills with attention to detailEffective written and verbal communication skillsAbility to manage multiple tasks and work in a fast-paced environmentABOUT PLANET PHARMAPlanet 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
