Project Manager

Latigo Bio; Thousand Oaks (CA); On-site; USD 120,000 - 180,000; Full time

Job summary

Latigo Biotherapeutics is seeking a Manager of Program Management to serve as the operational backbone of the acute pain program as the asset advances toward NDA submission and U.S. launch.

You will oversee cross‑functional program plans, coordinating regulatory, nonclinical, clinical, CMC/supply, quality, and commercial workstreams to keep the path to filing on track. The ideal candidate has a life sciences degree and at least six years in biotech/pharma with three years in drug development

Qualifications

• Bachelor's degree or higher in life sciences or related discipline.
• Minimum six years in biotechnology, pharmaceutical, or healthcare field with at least three years in drug development project management.
• Solid understanding of drug development and commercialization.

Responsibilities

• Accountable for integrated program plan and timelines across regulatory, nonclinical, clinical, CMC/supply, quality, and commercial workstreams.
• Drive decision-making and coordinate with the team to identify and resolve program or resource issues.
• Develop strategy with program teams and identify key program goals.
• Monitor and manage progress, schedules and resources to meet goals.
• Ensure plans are current and aligned with strategic shifts.
• Evaluate risks and ensure integration into program plans for monitoring deliverables.

Skills

Project management

Cross-functional collaboration

Regulatory knowledge

Communication

Leadership

Education

Bachelor's degree in life sciences

Job description

Job: Project Manager

Location: Thousand Oaks, CA or San Francisco CA

Position Type: Full Time

Reports to: 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 of 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 cross‑functional stakeholders, contribute to development strategy, and translate that strategy into execution. The successful candidate will bring a solution‑oriented attitude, a sharp eye for detail, and a willingness to learn in a team environment.

Primary responsibilities include (but are not limited to):

• Accountable for the integrated program plan and timelines across regulatory, nonclinical, clinical, CMC/supply, quality, and commercial workstreams; maintain scenario-based critical-path timelines from NDA submission through PDUFA and launch.
• Drive decision‑making and coordinate with the team or functional management to identify and resolve program or resource issues; monitor and manage program progress, schedules, and resources to meet or exceed program goals.
• Collaborate with program teams to develop strategy, and
  identify key program goals.
• 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.
• Serve as the program team’s single source of truth - convert meeting discussions into concise, decision- and action-oriented minutes and drive timely information flow so stakeholders and leadership stay aligned and institutional knowledge is captured and accessible.
• Support program budget development, tracking and variance management.
• As necessary, challenge teams by providing disconfirming information and encourage innovative problem-solving.

Basic Qualifications:

• B. A. degree or higher in life sciences or related disciplines.
• Minimum six (6) years’ experience within the Biotechnology, Pharmaceutical, or other Healthcare related field, with minimum three (3) years in direct drug development project management.
• Solid understanding of all aspects of drug development and commercialization.
• Proficient in project management principles and tools such as SmartSheet and Excel.
• Self‑motivated and highly flexible individual who is able to manage multiple tasks, and priorities within a fast‑paced environment with minimal oversight.
• Demonstrated ability to influence without authority.
• Excellent interpersonal, organizational, written and verbal communication skills.