Backed by 5AM Ventures.
About the role
Latigo Biotherapeutics is a private, early-stage biotechnology company discovering and developing the next generation of non-opioid medicines for pain and pain-related syndromes to transform the lives of patients . Latigo has a robust pipeline, is well-funded by blue chip investors, and has a highly successful management team and Board of Directors. The company was founded in 2019 and is based in Thousand Oaks, CA . We are science-based, data-driven, patient-focused, and forward-thinking.
What they're looking for
- Collaborate with program teams to develop strategy, and
- Monitor and manage program progress, schedules and resources to meet or exceed program goals
- Ensure program plans are current and in alignment with any strategic shifts
- Evaluate and communicate the probability and impact of risks, risk management plans and ensure integration into the overall program plans for monitoring deliverables
- Support program budget development, tracking and variance management
- As necessary, challenge teams by providing disconfirming information and encourage innovative problem - solving
More about this role
Job: Project Manager
Position t ype: Full Time
Reports t o : ED, Acute Program Lead
Organization Overview
Latigo Biotherapeutics is a private, early-stage biotechnology company discovering and developing the next generation of non-opioid medicines for pain and pain-related syndromes to transform the lives of patients . Latigo has a robust pipeline, is well-funded by blue chip investors, and has a highly successful management team and Board of Directors. The company was founded in 2019 and is based in Thousand Oaks, CA . We are science-based, data-driven, patient-focused, and forward-thinking.
Position Summary
Latigo is seeking a Manager o f Program Management to work closely with the Acute Program Lead and serve as the operational backbone of the acute pain program team as the asset advances toward NDA submission and U.S. launch. This role drives the development and execution of cross-functional program plans that enable the overall program strategy, coordinating regulatory, nonclinical, clinical, CMC/supply, quality, and commercial workstreams across the path to filing and the pre-launch build. Scientific competency and drug development knowledge are essential to interact with...
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