(contract) Director, Program Management at Centessa Pharmaceuticals, LLC

Boston, Massachusetts, United States -

Full Time

Start Date

Immediate

Expiry Date

17 Apr, 26

Salary

190.0

Posted On

17 Jan, 26

Experience

10 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Program Management, Drug Development, Risk Management, Budget Management, Cross-Functional Collaboration, Regulatory Submissions, Analytical Skills, Decision Making, Communication Skills, Leadership, Operational Excellence, Project Management, Vendor Management, Team Coordination, Issue Resolution, Dashboard Development

Industry

Biotechnology Research

Description

Centessa Pharmaceuticals plc (Nasdaq: CNTA) new kind of pharmaceutical company with a deconstructed R&D environment that prioritizes data driven decision making led by subject matter experts. Centessa is advancing a portfolio of high conviction programs with strong biological validation. Our asset-centric model offers a unique R&D logic that has been applied by single asset companies to improve productivity. This operating model has minimal centralized infrastructure, reduced hierarchy, and exclusive focus on data driven capital allocation. Our teams are uniquely incentivized to expeditiously interrogate key scientific hypotheses. We believe the asset-centric model can lead to improved success rates for programs with greater speed and modest costs. Director, Program Management (contract) Centessa Pharmaceuticals plc (Nasdaq: CNTA) new kind of pharmaceutical company with a deconstructed R&D environment that prioritizes data driven decision making led by subject matter experts. Centessa is advancing a portfolio of high conviction programs with strong biological validation. Our asset-centric model offers a unique R&D logic that has been applied by single asset companies to improve productivity. This operating model has minimal centralized infrastructure, reduced hierarchy, and exclusive focus on data driven capital allocation. Our teams are uniquely incentivized to expeditiously interrogate key scientific hypotheses. We believe the asset-centric model can lead to improved success rates for programs with greater speed and modest costs. Description of Role Centessa is seeking a (contract) Director of Program Management to manage one or more high complexity global R&D program. The Director, Program Management (PM) partners with the Global Team Leader (GTL) to lead cross‑functional planning and execution across the drug development lifecycle. Reporting to the Senior Vice President, Global Program Leadership, this role oversees creation and maintenance of fully integrated program plans, timelines, and risk‑management tools, ensuring clear communication of priorities, dependencies, and progress to teams and senior leadership. The (contract) Director of Program Management drives operational excellence by facilitating team meetings, managing dashboards, issues, and risks, coordinating budgets and vendor deliverables, and supporting governance and regulatory submission activities. Success requires strong collaboration, structured decision‑making, and the ability to lead complex programs in a fast‑paced environment. Key Responsibilities Partner with the GTL (Global Team Leader) to project manage a cross-functional matrix team, and select sub-teams Lead the development of and continuously maintain detailed and fully cross-functionally integrated program Gantt chart as a company-wide “Single Source of Truth,” 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 Bachelor’s degree in science or related field; advanced degree in a scientific discipline preferred 10+ year’s experience in pharmaceutical/biotech R&D environment, or MS/MBA plus 6+ years in pharmaceutical/biotech R&D environment, including 4+ years in program or project management PMP certification is highly desired 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, practices and standard project management tools Demonstrated ability to thrive in a fast-paced dynamic environment. Compensation The hourly rate for this position is $150.00 to $190.00. Individual compensation within this range will be determined based on a variety of factors, including qualifications, skills, relevant experience, and job knowledge. This position is a contract role and is not eligible for company employee benefits, including but not limited to health insurance, retirement plans, paid time off, or other employee programs. Individuals engaged in this role will be employed by and receive compensation through Centessa's designated employer of record. Work Location The (contract) Director, Program Management role is a remote role based in the US. EEOC Statement: Centessa Pharmaceuticals believes in a diverse environment and is committed to equal employment opportunity for all its employees and qualified applicants. We do not discriminate in recruitment, hiring, training, promotion, or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status. Centessa Pharmaceuticals will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law. Please note: We will not assign referral rights for any unsolicited resumes from recruitment agencies. EEOC Statement: Centessa Pharmaceuticals believes in a diverse environment and is committed to equal employment opportunity for all its employees and qualified applicants. We do not discriminate in recruitment, hiring, training, promotion, or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status. Centessa Pharmaceuticals will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law. Please note: We will not assign referral rights for any unsolicited resumes from recruitment agencies.

Responsibilities

The Director of Program Management will manage high complexity global R&D programs and partner with the Global Team Leader to lead cross-functional planning and execution. This role involves overseeing program plans, timelines, and risk management tools while ensuring clear communication of priorities and progress.