GSAM Global Study Asset Manager

Job details

Specialism: Clinical Operations

Expertise: Clinical Project Management

Location: Welwyn Garden City, Hertfordshire, England

Job type: Contract

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Description

Lead the operational engine behind molecule success and drive innovation across global clinical studies.

[Employer hidden — view at passion-project.co.uk] is seeking a Global Study Asset Manager (GSAM) to lead and drive the operational study management delivery of one or more molecule assets within the pharmaceutical industry. This role involves working closely with internal teams, cross-functional experts, and vendor partners to ensure smooth operational delivery. The GSAM will play a key role in ensuring consistency and efficiency across assigned studies while contributing to innovation in clinical operations.

Please note that to be considered for this role you must have the right to work in this location.

Responsibilities:

• Coordinate and deliver study management aspects for a group of studies within an asset portfolio, adhering to ICH-GCP and company SOPs.
• Provide input into essential study-level documents such as study protocols, training materials, and pharmacy manuals.
• Develop and maintain recruitment forecasts in collaboration with internal teams and CRO partners.
• Drive innovation in clinical operations by implementing new approaches to exceed industry best practices.
• Build strong partnerships with CROs and internal colleagues to ensure cost and resource efficiency.
• Oversee key performance indicators (KPIs) and proactively communicate risks or quality issues with proposed mitigations.
• Maintain inspection readiness for all components within the scope of responsibility.
• Lead third-party vendor selection, setup, oversight, and closeout to ensure delivery aligns with study needs.
• Manage supply and shipment of investigational medicinal products (IMP) and distribute patient and site-facing support materials.
• Regularly provide feedback to team members to support professional development and foster a high-performing organization.

Key Skills and Requirements:

• Minimum of 3 years of relevant operations experience; clinical trial management experience is a plus.
• University degree or equivalent experience, preferably in life sciences.
• Strong knowledge of drug development processes and regulations, including ICH and GCP guidelines.
• Self-starter with a passion for achieving successful outcomes and driving innovation.
• Growth mindset with a willingness to learn through experience.
• Comfortable working in fast-paced, collaborative environments.

For more information, please contact Mandi Cakwe.

If you are interested in applying to this exciting opportunity, then please click ‘Apply’ or to speak to one of our specialists visit the ‘Contact Us’ page.

[Employer hidden] is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. [Employer hidden] is acting as an Employment Agency in relation to this vacancy.

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##### Register your interest

If you can’t find your ideal role with us right now, we’d still love to hear from you! Send us your CV and we’ll contact you if a suitable role becomes available.

Register interest