CPMS Contract & Project Manager

The Project Management & Operations (PMO) Team within Precision Medicine Development (PMed) provides operational and program/project management support for clinical pharmacology biomarker project plans, translational research studies, and diagnostic (Dx). The team collaborate with various internal departments and external partners to progress Clinical Pharmacology Modelling & Simulation (CPMS), Clinical Biomarker & Correlational Sciences (CBCS) and Diagnostic (Dx) activities across the Respiratory, Immunology, and Infectious Disease (RIID) and Oncology portfolios. Specifically, the CPMS Contract/PM will ensure internal stakeholder alignments, create integrated project timelines, track project deliverables, identify and mitigate risks, and communicate with relevant stakeholders. Additionally, they will reconcile activities with contracting and finance operations and provide advice to the CPMS department and client groups. This will support decision-making with respect to outsourcing by developing detailed specifications, analyse proposals (for both service (activity) and cost provision), negotiate (both costs and content) and execute new and amended contracts that are robust, timely, and add significant opportunity for value generation to the business whilst minimising risk.,

• Vendor and Contract Management: Managing vendor contracts, approving invoices, and ensuring compliance with GSK policies and procedures. This also involves developing and negotiating clinical service provider contracts.
• Demonstrate broad knowledge of biomarker and pharmacokinetic outsourcing with awareness of Dx technologies, and IVD development.
• Project Management: Work with associate directors on cross-functional project teams to deliver clinical biomarker, Dx, and translational research objectives. This includes planning, tracking, and resolving operational problems to ensure timely completion of projects.
• Financial Oversight: Tracking and updating project budgets, milestones, and payments. Analyzing costs and providing comparisons with industry benchmarks.
• Risk Management: Identifying and communicating risks related to timeline, budget, and scope to stakeholders in a timely and clear manner.
• Collaboration and Communication: Working closely with internal teams and external partners to ensure project objectives are met. Regular communication of timelines, milestones, and goals to stakeholders is essential.
• Stakeholder Management: Develop key stakeholder relationships liaise between GSK and external suppliers to provide value-added customer service.
• Compliance and Documentation: Ensuring compliance with GSK policies and procedures, maintaining accurate records, and supporting regulatory submissions.
• Demonstrate the ability to take on new challenges and drive them to successful completion., We believe in an agile working culture for all our roles. If flexibility is important to you, we encourage you to explore with our hiring team what the opportunities are.
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• Bachelor's degree in biological sciences or related discipline; advanced scientific degree a plus
• Project or program management experience in the Dx, pharmaceutical, or biotech industry, clinical development
• Experience managing clinical biomarker, bioanalytical and/or In Vitro Dx development programs
• Experience managing third party vendors, vendor contracts and budgets including approval of invoices
• Understanding of drug discovery and development, clinical trial design, and overall principles of clinical development
• Established expertise and hands-on experience with Microsoft Project or equivalent, Word, Excel, PowerPoint, Outlook, SharePoint, remote meeting tools such as MS Teams, WebEx, etc. and a working understanding of innovative AI technologies (e.g., CoPilot, ChatGPT, GiGi, Jules, etc.)
Preferred Qualifications & Skills: Please note the following skills are not necessary, just preferred, if you do not have them, please still apply:
• Strategic thinking and ability to work effectively in a matrixed environment while managing multiple projects/competing initiatives simultaneously.
• Excellent time management, organizational skills, and results focused.
• Ability to establish trust, work with integrity, and motivate others to achieve project goals.
• Highly effective communication and negotiation skills for various audiences, including technical and business stakeholders.
• Financial analysis experience with a proven track record in budget management, contract financial analysis, and negotiation.
• Strong negotiation, influencing, analytical, problem-solving, and facilitation skills within the pharmaceutical or CRO industry.
• Knowledge of clinical pharmacology and the use of PK data to inform drug development programs.
• Experience in pharmaceutical development and companion Dx, including analytical and clinical validations and regulatory submissions.
• Good understanding and application of Project Management principles, concepts, practices, and standards; PMP certification and/or understanding of CPMS analysis including non-compartmental analysis techniques would be an advantage.
  
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