Global Study Manager

Hobson Prior are seeking a Global Study Manager to join the UK team at a world-wide pharmaceutical organisation focused on the research and development of novel medicines and marketing them once they have been developed.

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

Key Responsibilities:

• Develops operational plans including site monitoring strategies, risk mitigation strategies, trial budgets, site selection, and clinical supplies management.
• Builds and maintains effective and efficient high performing operations teams and ensures team members are aware of their accountabilities, responsibilities and deliverables.
• Creates team culture and promotes team spirit.
• Develops and maintains effective working relationships with Study Management Team (SMT) members, with particular focus on affiliate teams, external CRO (for outsourced teams) and co-development partner study teams.
• In collaboration with functional management, coaches, mentors, supports, and provides study specific direction to Study Management team members.
• Responsible for leading identification and selection of vendors; ensuring appropriate cross-functional input is incorporated into the scope of work.
• Responsible for assessing feasibility of and driving execution/adherence to protocol amendments or changes to clinical studies, across functions.
• Responsible for leading identification and selection of vendors; ensures appropriate cross-functional input into the scope of work.
• Designs drug assumption and supply chain process in partnership with Drug Supplies, affiliates and GSL.
• Oversees the forecasting and management of non-clinical supplies to ensure sites have supplies to run clinical study.

Requirements:

• Life sciences degree or nursing equivalent.
• Proven clinical development experience of the operational aspects of all stages of clinical studies preferably working in a Global environment and/or including monitoring or leading affiliate teams, working with vendors and/or CROs, drug supply management and planning operational activities to achieve database lock.
• Experience of project managing operational aspects of a clinical study including development and management of timelines and budgets.
• Good knowledge of ICH GCP.
• Proven ability to successfully achieve results within a multi-cultural and geographically diverse team.
• Experience of working as part of a large team and leading small study or functional teams, with a proven ability to be an active member of the team and motivate and lead a small team to deliver against commitments.
• Well-developed written and verbal communication skills demonstrated by an ability to present clear instruction/direction to teams at the same level in the organization and influence at higher levels in the organization.
• Strong attention to detail.
• Proficient computer skills.

Apply now:

If you are interested in learning more or applying to this exciting opportunity then please click "Apply" and upload a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist directly, please select "Contact me" at the top of this page.

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