10 часов назад
Program Manager, Preclinical & Early Development (Biopharma)
223 000 - 247 200$
Мэтч & Сопровод
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Описание вакансии
Текст:
TL;DR
Program Manager, Preclinical & Early Development (Biopharma): Building and maintaining integrated plans for IND-enabling and early clinical programs while coordinating cross-functional scientific and operational work with an accent on timelines, dependencies, critical paths, and governance. Focus on documenting decisions, tracking risks and commitments, forecasting resources, and managing collaboration with external partners.
Location: Onsite in Brisbane, California, United States, at least five days per week
Salary: $223,000–$247,200 per year
Company
is a clinical-stage biopharmaceutical company developing targeted protein degradation medicines for cancer and inflammatory diseases through an AI-integrated discovery engine.
What you will do
- Build and maintain integrated project plans covering timelines, milestones, resourcing, dependencies, and critical paths for preclinical and early development programs.
- Coordinate planning across Research, Translational Sciences, Discovery Biology, Medicinal Chemistry, DMPK, Nonclinical Safety, CMC, Clinical Development, Clinical Operations, Regulatory Affairs, and Biometrics.
- Facilitate cross-functional meetings, document decisions, maintain action logs, and follow up on commitments.
- Manage the day-to-day rhythm of partnered governance committees, including agendas, meeting materials, minutes, repositories, rosters, and subteams.
- Track and escalate risks and issues, develop contingency plans, and prepare status reports, dashboards, and governance materials.
- Support program-level resourcing and forecasting and improve project management tools, templates, and processes.
Requirements
- Master’s degree in life sciences, engineering, or a related technical field; an advanced degree is a plus.
- 7+ years of project or program management experience in a biotech, pharmaceutical, or CRO setting, spanning discovery through translational and early clinical development.
- Experience creating integrated project plans, realistic timelines, dependency maps, and critical paths from technical or scientific input.
- Strong meeting facilitation, written and verbal communication, judgment, organization, and decision-making skills.
- Ability to work effectively with scientists, functional leads, senior leadership, and external partners without formal authority.
Nice to have
- Experience in immunology, oncology, clinical pharmacology, or another complex therapeutic area.
- Experience with formal external-partner governance structures, alliance management, or project management organizations.
- PMP or equivalent project management certification.
- Experience working in an evolving project management capability.
Culture & Benefits
- Highly collaborative, team-oriented working environment.
- Solutions- and results-oriented approach.
- Hands-on, resourceful work style with openness to diverse points of view.
- Onsite work at the Brisbane headquarters is expected at least five days per week.
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