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Associate Director/Director, Program Management


Werewolf Therapeutics is an exciting, public, biotherapeutics company located in the heart of the Boston/Watertown area biotech hub, focusing on the development of novel biologic agents targeting immune regulatory pathways for the treatment of cancer. 


Lead project/program management efforts associated with all development activities to support advancement of programs towards company goals.


Reasonable Accommodations Statement

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. Reasonable Accommodations may be made to enable qualified individuals with disabilities to perform the essential functions.

  • Lead cross-functional program teams across all R&D (CMC, Non-Clinical, Clinical, QA) and Discovery efforts and initiatives to support program advancement.
  • Provide project coordination and communication in support of multiple development projects including participation in technical calls, tracking of action items, and facilitating rapid decision making within the team to drive programs forward.
  • Support functional areas in developing and executing strategy and operating plans.
  • Assist functional areas with requisition management, including supporting accrual inquiries from the Finance team.
  • Develop, maintain, and manage integrated program timelines, including identifying critical paths and roadblocks, minimizing risks, identifying mitigation plans and options.
  • Work with functional area team members and the Finance team to develop and oversee budgets/forecasts and ensuring they are aligned with overall strategy and timelines.
  • Work with PM team members to develop and implement project management initiatives and tools, as appropriate.
  • Support writing, review, publication and filing of Regulatory documents and health authority interactions to support submission of INDs, NDAs, etc.
  • Facilitate collaboration and problem-solving.
  • Facilitate communication to ensure alignment.



  • B.S or M.S. degree in science or related discipline.

Experience and Requirements:  

  • At least 7 years of experience in the biotechnology or pharmaceutical industry.
  • Minimum of 5 year’s experience in project or program management at a biotechnology or pharmaceutical company with involvement in early-stage programs.  Experience in oncology a plus.
  • Strong understanding of the drug development and Regulatory processes.
  • Familiarity with GMP environment and requirements.
  • Experience working in cross functional environments including managing projects within an outsourced operational model.


  • Experience with project management (e.g. MS Project, Excel) and collaboration tools (e.g. SharePoint, Box, MS Teams, Zoom) is essential.
  • Good communication, written and presentation skills.
  • Ability to work independently and proactively.
  • Ability to follow-thru and follow-up on items as needed.
  • Ability to prioritize activities in complicated programs.
  • Ability to combine attention to detail and big picture perspective.


  • Work is normally performed in a typical interior/office/lab work environment.
  • None or very limited physical effort required.
  • Work environment involves some exposure to hazards or physical risk, which require following basic safety precautions.


For further information or to be considered for this position, please

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