(Associate) Director, Project Management

Centessa Pharmaceuticals, a wholly owned subsidiary of Eli L

$115K — $170K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • BS plus 8+ years or MS/MBA plus 6+ years in pharma/biotech R&D
  • 4+ years in project management or equivalent role
  • Experience with IND-enabling activities and Phase 1 development
  • Proven expertise in drug development and global regulatory interactions
  • Strong communication and collaboration skills with ability to lead without formal authority
  • Expertise in project management software; PMP certification preferred

Responsibilities

  • Partner with Global Team Leader to manage cross-functional development teams
  • Lead creation and maintenance of integrated program Gantt chart
  • Identify interdependencies and manage risks to support scenario planning
  • Develop dashboards to communicate program status and track progress
  • Schedule and manage cross-functional team meetings and follow-up actions
  • Maintain issue logs and risk registers for proactive resolution
  • Work with Finance to develop and monitor program budgets
  • Manage external vendors to integrate deliverables into program Gantt
  • Support preparation of regulatory submission documents
  • Contribute to refining processes and best practices

Benefits

  • Comprehensive benefits package including medical, dental, vision, and life insurance
  • 401(k) plan participation
  • Generous paid time off policy
  • Health and wellness program
  • Discretionary annual bonus eligibility
Full Job Description
Description of Role

Centessa is seeking a (Associate) Director, Program Management - Orexin Development Programs. This individual will leverage both project management and drug development experience to manage one or more early-stage global Orexin development programs. This position will report to the Executive Director, Global Team Leader.

Key Responsibilities
  • Partner with the GTL (Global Team Leader) to project manage a cross-functional matrix development team, and select sub-teams
  • Lead the development of and continuously maintain detailed and fully cross-functionally integrated program Gantt chart, incorporating all relevant dependencies, and provide fit-for-purpose summary views for team use and executive management reviews
  • Identify and manage interdependencies, critical path and at-risk activities to support program level scenario planning and risk management strategies
  • Develop and maintain relevant dashboards to communicate status and track progress
  • Manage cross-functional team meetings including scheduling, preparing agendas, presentation materials, and minutes that ensure proper follow up of action items
  • Develop and maintain issue logs and risks registers, and ensure team proactively resolve issues in a timely manner and that risks are mitigated as appropriate
  • Work with cross-functional team and Finance to develop and update budgets, and manage program spend within approved budget
  • Manage select external vendors (timelines, budgets, MSA/SOW documents, etc.) and integrate deliverables into program Gantt
  • Support development of Governance and Executive presentations
  • Provide support for the planning and preparation of documents to a quality standard required for Regulatory/Health Authority submissions
  • Contribute to establishment and refinement of best practices, processes and procedures

Qualifications
  • BS plus 8+ years' experience in pharmaceutical/biotech R&D environment, or MS/MBA plus 6+ years in pharmaceutical/biotech R&D environment, including 4+ years as PM or equivalent
  • Experience managing project teams through IND-enabling activities, pre-IND mtgs, IND submissions, and Phase 1 development.
  • 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 optimal team performance
  • Excellent analytical skills and expert in facilitating team decision making; competent in the application of decision analysis methodologies and related tools
  • Expert knowledge of project management principles and practices with the ability to thrive in a fast-paced dynamic environment (PMP certification is highly desired), and expert in project management software, e.g., Smartsheet

Work Location

The (Associate) Director, Project Management role is based in the US, with occasional travel.

Compensation

The annual base salary range for the Associate Director level position is $115,000 -$170,000.

The annual base salary range for the Director level position is $130,000 - $210,000

Individual compensation within this range will be determined based on a variety of factors, including qualifications, skills, relevant experience, job knowledge and location.

In addition to base pay, this role is eligible for a discretionary annual bonus. Centessa also offers a comprehensive benefits package, which includes a 401(k) plan, company-sponsored medical, dental, vision, and life insurance, generous paid time off, and a health and wellness program.

POSITION: Full-Time, Exempt

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