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18 часов назад

Director, Project Management Search & Evaluation (Biotech)

234 000 - 260 000$
Формат работы
hybrid
Тип работы
fulltime
Грейд
director
Английский
b2
Страна
US/Australia
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
Director, Project Management Search & Evaluation (Biotech): Leading search and early due diligence projects for external biopharma innovation opportunities with an accent on cross-functional evaluation, governance, and strategic partnering. Focus on coordinating scientific, clinical, regulatory, IP, legal, and commercial workstreams, managing risks and timelines, and providing decision-support materials for senior leadership.

Location: Hybrid role based in King of Prussia, Pennsylvania, or Waltham, Massachusetts, with onsite work required three days per week.

Salary: $234,000–$260,000 base salary per year, with potential incentive compensation and equity.

Company

hirify.global is a global biotechnology company developing and delivering therapies, vaccines, and other medicines across rare and serious diseases, influenza, iron deficiency, and nephrology.

What you will do

  • Lead project management for external innovation search activities, including scouting, landscape assessments, and initial opportunity evaluation.
  • Manage early-stage due diligence for potential in-licensing, acquisition, and partnership opportunities.
  • Coordinate integrated evaluations across scientific, clinical, regulatory, CMC, IP, legal, and commercial workstreams.
  • Prepare governance meetings, presentations, dashboards, status reports, and decision-support materials for senior leadership.
  • Facilitate collaboration among Search, R&D, Business Development, Legal, Finance, external partners, and other stakeholders.
  • Improve search and due diligence workflows through new tools, evaluation platforms, AI-enabled search capabilities, and lessons learned.

Requirements

  • 12+ years of experience in biopharma, including 8+ years managing complex cross-functional program projects under tight timelines.
  • Experience in project leadership and Search & Evaluation, Business Development & Licensing, or external innovation.
  • Experience orchestrating asset due diligence across scientific, clinical, CMC, regulatory, IP, legal, and commercial areas.
  • Strong understanding of drug development processes, external innovation strategies, valuation drivers, and deal critical paths.
  • Excellent communication, negotiation, and stakeholder management skills.
  • Advanced degree preferred, such as PhD, PharmD, MD, MSc, or MBA.

Nice to have

  • PMP or equivalent certification.
  • Proficiency with InPart or similar partnering platforms and Microsoft Teams or SharePoint.
  • Experience with AI-assisted landscaping and evaluation tools.

Culture & Benefits

  • Work in a project-led R&D organization focused on collaboration and innovation.
  • Contribute to therapies and medicines intended to address unmet medical needs.
  • Benefits information is provided through CSL's employee well-being program.
  • Inclusion and belonging are emphasized as part of the workplace culture.
  • Total compensation may include incentive compensation and equity in addition to base salary.

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