Director of Program and Alliance Management (Biotech)

Associate Director/ Director, Alliance and Program Management
Greater Boston Area

Responsibilities (include, but not limited to):

  • Serve as a collaborative member of the alliance and program management team to manage multiple key partnerships and a significant number of programs while building and maintaining processes to support the group and the organization
  • Lead cross-functional program teams/meetings that may include representatives from research, nonclinical development, regulatory, CMC, and clinical development to define the most appropriate drug development strategy
  • Support cross-functional teams and stakeholders to facilitate technical and scientific discussions that define the product profile, integrated development plans, schedule and budget for various internal and partnered programs
  • Mobilize and align the organization to drive decision-making and implement the development strategy
  • In collaboration with the scientific/development leads, facilitate team meetings and documentation, decision making and tracking of milestones, critical path, timelines, risks, assumptions, alternative scenarios, and budgets
  • Foster strong relationships within the organization and serve as a critical point person for program team members (in conjunction with scientific or development leads) on portfolio and program strategy, project-related communications, scientific discussions, issue identification, and management
  • Manage alliance(s) with pharma partners to ensure strategic and operational alignment on discovery through clinical-stage programs in neurology, oncology, and autoimmune
  • Effectively communicate with senior management on program strategy, progress, and timelines

Education/Skills/Experience Requirements:

  • Degree in life sciences; advanced degree, Ph.D. or MBA preferred
  • Eight plus years of total industry experience, including at least five years in a project management role (title commensurate with experience)
  • Strong understanding of cross cross-functional drug development from preclinical through early clinical development (including an understanding of GxP, and experience with IND submissions)
  • Strong leadership skills, with the ability to influence at all levels of an organization
  • Experience in the application of program management principles required
  • Proficient in MS Office (including Project, Word, Excel, and PowerPoint) and experience with timeline management tools (e.g. MS Project, Smartsheets), required
  • Excellent oral and written communication skills, including presentation and facilitation
  • Excellent record-keeping abilities and attention to detail
  • Commitment to a high-performing, patient & people-first culture, where there is alignment around a common vision and individuals are supported in their growth path