CPMS Contract Manager

3 weeks ago

Stevenage, Hertfordshire, United Kingdom GSK Full time
Job Description

Job Title: CPMS Contract Manager

Job Summary:

We are seeking a highly skilled CPMS Contract Manager to join our team at GSK. The successful candidate will be responsible for managing clinical biomarker, bioanalytical, and In Vitro Dx development programs, as well as vendor contracts and budgets.

Key Responsibilities:

  • Vendor and Contract Management: Manage vendor contracts, approve invoices, and ensure compliance with GSK policies and procedures.
  • Project Management: Work with associate directors on cross-functional project teams to deliver clinical biomarker, Dx, and translational research objectives.
  • Financial Oversight: Track and update project budgets, milestones, and payments.
  • Risk Management: Identify and communicate risks related to timeline, budget, and scope to stakeholders.
  • Collaboration and Communication: Work closely with internal teams and external partners to ensure project objectives are met.
  • Stakeholder Management: Develop key stakeholder relationships and liaise between GSK and external suppliers.
  • Compliance and Documentation: Ensure compliance with GSK policies and procedures, maintain accurate records, and support regulatory submissions.

Requirements:

  • 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.

Preferred Qualifications:

  • 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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