3 дня назад
Executive Director, Development Asset Lead (Biotech)
332 000 - 469 250$
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
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
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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