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3 дня назад

Executive Director, Development Asset Lead (Biotech)

332 000 - 469 250$
Формат работы
onsite
Тип работы
fulltime
Грейд
director
Английский
b2
Страна
US
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
Executive Director, Development Asset Lead (Biotech): Leading Development Asset Leads and shaping integrated development strategies for innovative therapies across clinical-stage and marketed assets with an accent on portfolio strategy, clinical development, regulatory planning, and resource allocation. Focus on guiding IND-enabling work, first-in-human studies, proof-of-concept generation, lifecycle planning, and complex portfolio governance decisions.

Location: Cambridge, MA, United States

Base salary: $332,000–$469,250 per year

Company

hirify.global is a mid-sized biotechnology company developing life-changing medicines across multiple therapeutic areas and modalities.

What you will do

  • Lead, mentor, and develop a team of Development Asset Leads.
  • Establish best practices for matrixed team leadership, communication, and portfolio value, risk, and cost management.
  • Guide teams through IND-enabling activities, first-in-human studies, proof-of-concept generation, lifecycle planning, and regulatory interactions.
  • Develop integrated asset plans that align clinical, scientific, business, and portfolio strategies.
  • Balance scientific opportunity, risk, probability of success, competitive differentiation, and resource allocation.
  • Represent assets with senior stakeholders and at portfolio governance forums while supporting portfolio decisions.

Requirements

  • Bachelor’s degree required; an advanced degree such as MS, MD, PhD, PharmD, or MBA is strongly preferred.
  • At least 13 years of drug development experience in pharma or biotechnology.
  • Strong people management skills and proven strategic leadership in cross-functional or portfolio roles.
  • Experience creating and executing clinical development plans aligned with broader business strategies.
  • Strong scientific and clinical judgment, learning agility, and understanding of competitive and business implications of scientific data.
  • Experience working in matrix leadership environments and navigating complex decision-making processes.

Nice to have

  • Understanding of Minimum and Target Product Profile concepts.
  • Knowledge of regulatory requirements for drug development and registration.
  • Experience with early clinical studies, clinical proof-of-concept, complex pipeline strategy, and regulatory submissions.
  • Participation in NDA, BLA, MAA, or equivalent regulatory submissions.

Culture & Benefits

  • Regular employee position with short- and long-term incentives, including cash bonuses and equity opportunities.
  • Medical, dental, vision, life, disability, and wellness benefits.
  • Paid vacation, company holidays, personal-significance days, sick time, and parental leave.
  • 401(k) program with company matching contributions and an employee stock purchase plan.
  • Tuition reimbursement of up to $10,000 per calendar year.
  • Inclusive environment focused on collaboration, learning, growth, and employee resource groups.

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