Global Studies Asset Manager

Adecco Portugal

Welwyn

Hybrid

GBP 117,000 - 130,000

Full time

6 days ago
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Job summary

Adecco is recruiting for a Global Studies Asset Manager (GSAM) on behalf of a leading pharmaceutical client. Based in Welwyn, England, this hybrid, 6-month contract will oversee operational study management of molecule assets and drive global clinical trials delivery.

You will coordinate study management across assets, develop study documents, collaborate with APO teams, monitor KPIs, manage vendor relationships, and contribute to continuous improvement in clinical operations.

Qualifications

  • Relevant operations experience in clinical trial management is desirable.
  • Bachelor's degree or equivalent, preferably in life sciences.
  • Knowledge of drug development process and ICH/GCP guidelines.
  • Strong collaboration and vendor management experience.
  • Experience leading components of study delivery including vendor oversight and budget reconciliation.
  • Phase 3 clinical trial experience across multiple disease areas preferred.

Responsibilities

  • Coordinate and oversee study management across multiple studies within an asset portfolio per ICH-GCP and company processes.
  • Develop study documents (protocols, training materials) with cross-functional teams and external partners.
  • Collaborate with Analytics and APO teams to improve efficiency and patient-centric study delivery.
  • Monitor KPIs related to operational quality and timelines; address risks proactively.
  • Build and maintain relationships with internal stakeholders and external vendors throughout the study lifecycle.
  • Contribute to innovative approaches in clinical operations and continuous improvement.

Skills

Clinical operations
Vendor management
Cross-functional collaboration
Study management
Budget reconciliation

Education

Life sciences degree

Job description

Job Title: Global Studies Asset Manager (GSAM)

Location: Welwyn, England; Hybrid

Daily Rate: 450 - 500

Working Pattern: Full Time

Contract: 6 months

Exciting Opportunity in Pharmaceutical Development!

Our client, a leading player in the pharmaceutical industry, is seeking a Global Studies Asset Manager to drive the operational study management of innovative molecule assets. This pivotal role will involve leading clinical operations management and ensuring the successful delivery of global clinical trials.

Key Responsibilities:
  • Coordinate and oversee the study management aspects of multiple studies within an asset's portfolio, adhering to ICH-GCP and company processes.
  • Develop essential study documents, including study protocols and training materials, in collaboration with cross-functional teams and external partners.
  • Collaborate with Analytics and Portfolio Optimisation (APO) teams to enhance efficiency and ensure a patient-centric approach in study delivery.
  • Monitor and report on key performance indicators (KPIs) related to operational quality and efficiency, proactively addressing any risks to timelines or quality.
  • Build and maintain relationships with internal stakeholders and external vendors, ensuring effective communication and collaboration throughout the study lifecycle.
  • Contribute to the development of innovative approaches in clinical operations, driving continuous improvement and aligning with industry best practises.
Qualifications:
  • Relevant operations experience in clinical trial management is highly desirable.
  • A university degree or equivalent experience, preferably in life sciences.
  • Strong working knowledge of the drug development process and applicable regulations, including ICH and GCP guidelines.
  • Excellent collaboration skills with experience in cross-functional communication and vendor management.
  • Demonstrated ability to lead various components of study delivery, such as vendor oversight and budget reconciliation.
  • Phase 3 clinical trial experience is mandatory, with a preference for candidates with exposure across multiple disease areas.
Why Join Our Client?
  • Contribute to transformative medicines that address high societal burdens by 2029.
  • Engage in a vibrant and collaborative work environment that values innovation and professional growth.
  • Work within a dynamic team that is dedicated to improving patients' lives around the world.

If you are a proactive self-starter with a passion for clinical operations and a desire to make a meaningful impact, this is an outstanding opportunity to advance your career in a forward-thinking organisation.

We use generative AI tools to support our candidate screening process. This helps us ensure a fair, consistent, and efficient experience for all applicants. Rest assured, all final decisions are made by our hiring team, and your application will be reviewed with care and attention.

Adecco is a disability-confident employer. It is important to us that we run an inclusive and accessible recruitment process to support candidates of all backgrounds and all abilities to apply. Adecco is committed to building a supportive environment for you to explore the next steps in your career. If you require reasonable adjustments at any stage, please let us know and we will be happy to support you.

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