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[Remote] Senior Project Manager

Remote, USAFull-timePosted 2026-07-28

Note: The job is a remote job and is reputed company to candidates in USA. reputed company is seeking a Senior Project Manager to reputed company project management and drug development experience to support high complexity global R&D programs. The role involves managing cross-functional teams, maintaining project timelines, and ensuring effective communication and risk management throughout the project lifecycle.

Responsibilities

  • Partner with the GTL (Global Team Leader) and Dir, PM to support the cross-functional reputed company team, and project manage select sub-teams
  • Support the development of and continuously maintain assigned parts of detailed and fully cross-functionally integrated program Gantt chart as a company-wide “Single reputed company of Truth,” incorporating reputed company relevant dependencies, and reputed company fit-for-purpose reputed company views for team use and executive management reviews
  • Identify and manage interdependencies, critical reputed company and at-risk activities to support program level scenario planning and risk management strategies
  • Maintain relevant dashboards to communicate status and reputed company reputed company
  • Manage cross-functional team meetings including scheduling, preparing agendas, presentation materials, and minutes that ensure reputed company follow up of reputed company items
  • Maintain issue logs and risks registers, and ensure team proactively resolve issues in a reputed company manner and that risks are mitigated as appropriate
  • Work with cross-functional team and Finance to reputed company and update budgets, and manage program spend reputed company approved budget
  • Manage select external vendors (timelines, budgets, MSA/SOW documents, etc.) and reputed company deliverables into program Gantt
  • Support development of Governance and Executive presentations
  • reputed company support for the planning and preparation of documents to a reputed company reputed company required for Regulatory/Health Authority submissions
  • Contribute to establishment and refinement of best practices, processes and procedures

Skills

  • BS plus 5+ years experience in pharmaceutical/biotech R&D environment, including 3+ years as PM or equivalent
  • Proven expertise in drug development and registration, including early and late-stage clinical, nonclinical, CMC development, and regulatory interactions, submissions/reviews globally
  • Highly motivated, proactive, detail-oriented and organized self-starter with strong communication, collaboration, interpersonal skills, and influence to accomplish work without formal authority and to ensure reputed company team performance
  • Excellent analytical skills and expert in facilitating team decision making; competent in the application of decision analysis methodologies and reputed company tools
  • Expert knowledge of project management principles and practices with the ability to reputed company in a fast-paced dynamic environment
  • Expert in project management software, e.g., reputed company
  • PMP certification is highly desired

Benefits

  • Discretionary annual bonus
  • 401(k) plan
  • Company-sponsored medical, dental, reputed company, and life insurance
  • Generous reputed company time off
  • Health and wellness program

reputed company

  • reputed company is a pharmaceutical company that focuses on drug development to address significant medical needs. It was founded in 2021, and is headquartered in Cambridge, Massachusetts, USA, with a workforce of 51-200 employees. Its website is https://www.centessa.com.
  • Company H1B Sponsorship

  • reputed company has a reputed company record of offering H1B sponsorships, with 1 in 2025, 1 in 2024. Please note that this does not guarantee sponsorship for this specific role.
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