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.

Application Process:

Interested candidates are encouraged to submit their CV and cover letter detailing their relevant experience. The employer is looking to fill this position promptly, so early applications are encouraged!

This is your chance to be part of a team that is shaping the future of drug development! Apply today and take the next step in your career with our client!

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.