Job Description

Global Study Asset ManagerContract | 6 months | Full-time Hybrid - Welwyn Garden City (minimum 2 days on site)Inside IR35 (Umbrella)The OpportunityWe are supporting a global pharmaceutical organisation within Pharma Product Development / Global Clinical Operations to appoint an experienced Global Study Asset Manager. This is a hands-on contract role focused on the operational delivery of global clinical studies across a molecule asset or portfolio of studies.You will play a key role in ensuring studies are delivered efficiently, compliantly, and inspection-ready, working closely with cross-functional stakeholders and CRO partners.Key ResponsibilitiesLead and coordinate operational study management across one or more global studies within an asset portfolio, in line with ICH-GCP, SOPs, and internal processesPartner closely with global study leaders, operations asset leaders, CROs, and country teams to ensure consistent deliveryContribute to and maintain essential study-level documentation (e.g. protocol input, TMP, pharmacy manuals, study plans, training materials)Develop and maintain study recruitment forecasts in collaboration with internal teams and CRO partners using appropriate systemsOversee operational KPIs, quality metrics, and risk management, proactively escalating issues and proposing mitigationsMaintain inspection readiness through strong documentation discipline and system accuracyLead vendor selection, set-up, oversight, and close-out, ensuring delivery to contract and alignment with integrated operations plansManage practical operational elements including IMP supply and shipment, patient and site materials (including translation), and clinical trial insuranceExperience & QualificationsEssential:Minimum 3 years' relevant clinical operations experience, ideally within global study deliveryStrong working knowledge of the drug development process and applicable regulations, including ICH and GCPProven experience working with and overseeing CRO partners and third-party vendorsDemonstrated ability to manage study delivery, forecasting, KPIs, and inspection readinessDegree in life sciences or a related field (or equivalent experience)Desirable:Direct global clinical trial management experience (beyond site or local operations)Experience working within large pharma or complex global trial environmentsComfortable operating in fast-paced, highly collaborative, and sometimes ambiguous settingsWho This Role SuitsA confident, hands-on clinical operations professional who can own operational delivery with minimal supervisionSomeone structured, systems-driven, and comfortable managing multiple stakeholders and vendorsA professional who values transparency, quality, and proactive problem-solvingRight to WorkApplicants must have the right to work in the UK.No sponsorship available.

Skills Required