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Head of CMC and Non-clinical Project Management
2 months ago
We are seeking a highly experienced and skilled Head, CMC & Non-clinical Project Management to lead our project management function in Medicine, Development & Supply (MDS). This role will be responsible for setting the standard of excellence for professional project management of complex technical projects, ensuring plans and forecasts are designed and executed in alignment with the project strategy.
Key Responsibilities:- Lead the CMC & NC PM, MDS project management function supporting the whole R&D portfolio from peri-CS through to post-launch.
- Develop, implement and maintain a project planning and management capability (tools, processes, ways of working, people) to enable and deliver the technical and supply aspects of all GSK's Pharma R&D pipeline medicines effectively and productively.
- Maintain awareness of internal and external project management practice to ensure currency of MDS's approach and work to continuously improve the competency level of project management across CMC & NC PM, MDS.
- Maintain awareness of platform technology, CMC, supply chain, non-clinical safety and DMPK trends to ensure work package libraries and project plans are fit for purpose.
- Provide operational input and review to ensure PM resource allocation is in alignment with project and portfolio workload forecasts and priorities across the R&D portfolio.
- Be the point of contact for all partners and stakeholders (e.g. R&D Project Management, Finance, Global Supply Chain) to drive consistent, integrated, strategic project and resource management across CMC & NC PM, MDS.
- Bachelor's degree in a life sciences or business discipline.
- 10+ years experience in pharmaceutical R&D or pharmaceutical manufacturing, with 5+ years experience in project management.
- Experience leading a global function consisting of 25+ team members.
- MSc or PhD degree in scientific or engineering discipline together with substantial industry experience, preferably with CMC or other Pharma platform technology experience.
- In depth understanding of drug development processes, regulations, and requirements with a good awareness of medicine commercialization.
- Ability to build credibility quickly across a diverse range of teams, seniority, and geography with high level of personal integrity plus ability to handle highly confidential information appropriately.
- Ability to employ highly effective decision-making strategies with sound technical and business judgement to resolve issues and conflicting options with high risk / impact to the organization.
- Highly effective influencing and negotiations skills in challenging, ambiguous and/or changing environments, with or without formal authority and across all levels of an organization.
- Ability to work with project teams and senior leadership teams to identify novel solutions to both project-specific and portfolio wide issues.
