Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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Зарплата и рынок
Выше рынка
$148к-185к/год
$120к$140кмедиана$170к
По похожим ролям (49) ~ $140к/год
На СНГ рынке: $3.5к/мес ($2.2к - $5.6к)
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Крутая вакансия
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Чётко очерченная senior-роль в AI-биотех стартапе даёт заметную ответственность за ведущую программу разработки биопрепарата, а базовая зарплата выше ориентира платформы и дополняется бонусом и акциями; главный компромисс - обязательная работа в офисе.
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Только офисЗарплата выше рынкаAI в биотехеПонятная зона ответственностиТемп стартапа
Оценка от Hirify AI
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Senior Project Manager, Biologics R&D – Lead Program (Biologics R&D): Managing a lead T-cell engager program from late-stage research through development candidate nomination and IND-enabling studies with an accent on integrated planning, biologics R&D execution, and cross-functional coordination. Focus on pressure-testing timelines, managing CRO and CDMO workstreams, tracking risks and budgets, and preparing decision-ready data for development milestones.
Location: On-site in South San Francisco, California, United States; remote candidates will not be considered.
Base salary: $148,000–$185,000 annually, plus bonus and equity.
Company
hirify.global is a biotech startup using generative AI and foundation models for biology to develop protein and antibody therapeutics and improve drug discovery and development.
What you will do
Own day-to-day planning and execution for a lead T-cell engager program from late-stage research through development candidate nomination and IND-enabling studies.
Build and maintain integrated timelines covering research, nonclinical, CMC, regulatory workstreams, critical paths, milestones, dependencies, and deliverables.
Partner with scientific and functional leads to define decisive experiments, pressure-test assumptions, and prepare go/no-go decision packages.
Coordinate cross-functional meetings, document decisions, track action items, and resolve interdependencies across workstreams.
Manage outsourced CRO and CDMO activities, including GLP toxicology, cell line development, process development, timeline integration, and issue escalation.
Own risk management, scenario planning, resource coordination, budget tracking, and spend forecasting.
Requirements
6+ years of industry experience in biologics R&D, including 3+ years in project or program management with ownership of integrated program plans.
Experience managing antibody or protein therapeutic programs from research through development candidate nomination and IND-enabling studies.
Working fluency in nonclinical development, CMC, cell line development, process development, developability, and regulatory activities.
Experience managing outsourced work with CROs and/or CDMOs.
Strong analytical, planning, organizational, communication, collaboration, and stakeholder management skills.
Ability and willingness to work on-site in the South San Francisco office.
Nice to have
Advanced degree in life sciences or a related field.
Experience with T-cell engagers, bispecific antibodies, or other immuno-oncology biologics.
Completed IND filing experience.
PMP, CAPM, or PMI-ACP certification.
Experience working in a fast-paced startup environment and leading without authority.
Culture & Benefits
Open, flexible, and collaborative work environment.
Competitive compensation and benefits package.
Base salary plus bonus and equity.
Opportunity to contribute to innovative biologics development and improved patient outcomes.
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