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Senior Manager/Associate Director, Program Management

Tenvie Therapeutics

Brisbane, CA

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JOB DETAILS
JOB TYPE
Full-time
SKILLS
Biology, Biotech and Pharmaceutical, Business Administration, Cardiovascular Disease, Chemistry, Communication Skills, Contract Research Organization (CRO), Cross-Functional, Decision Support, Detail Oriented, Disease, Documentation, Drug Development, Identify Issues, Investment Management, Leadership, Multiple Sclerosis, Neurology, Obesity, Organizational Skills, Plan Meetings, Pre-Clinical Development, Presentation/Verbal Skills, Problem Solving Skills, Program Planning, Project Management Software, Project Planning, Project/Program Management, Regulations, Risk Analysis, Small Molecules, Strategic Planning, Translational Research, Writing Skills
LOCATION
Brisbane, CA
POSTED
30+ days ago

Senior Manager/Associate Director, Program Management

Tenvie Therapeutics is developing precision‑engineered small molecule therapies to address core drivers of neurological and peripheral diseases: neuroinflammation and cellular dysfunction. Leveraging its proprietary product engine, Tenvie has the unique ability to advance both fully CNS‑penetrant and peripherally restricted products across a broad portfolio. Tenvie’s most advanced program, TNV262, a fully CNS-penetrant NLRP3 inhibitor, is in Phase 1 clinical development for cardiometabolic indications, including obesity and cardiovascular disease, as well as multiple sclerosis. In parallel, Tenvie is advancing TNV108, a peripherally restricted SARM1 allosteric inhibitor targeting peripheral neuropathies, through preclinical development. Tenvie’s clinical pipeline is complemented by discovery-stage programs across a range of related indications.
Tenvie Therapeutics is seeking a highly motivated, organized, and scientifically grounded individual to join our team as a critical cross-functional “integrator”.  This role is ideal for candidates with a strong scientific background who have worked cross-functionally in a research or development environment and are eager to take on a more program-oriented leadership role.  The ideal candidate will have a strong background in early-stage drug development and will help coordinate activities across multiple functions (biology, chemistry, translational sciences, regulatory, clinical, etc.), ensuring alignment, clarity of goals, and efficient execution of early development strategies. We are seeking a general athlete skillset with agility to learn on the run, build strong relationships across functions, and drive program success. This position reports to the Vice President of Program and Portfolio Management.

JOB RESPONSIBILITIES:
  • Partner with program leads to plan, track, and drive the progress of early-stage drug development programs
  • Facilitate cross-functional collaboration across research, preclinical, and development teams
  • Develop and maintain integrated program timelines, identifying risks, dependencies, and critical path activities
  • Ensure clear communication of program status, key milestones, and risks to internal stakeholders and leadership
  • Support decision making by organizing data, preparing summaries, and coordinating review meetings
  • Drive operational excellence by implementing structured processes, documentation practices, and meeting cadences
  • Identify potential bottlenecks and proactively propose solutions to keep programs on track
  • Coordinate with external collaborators, CROs, and partners as needed
  • Help ensure alignment between scientific objectives and development plans










QUALIFICATIONS: 
  • Preferred advanced degree (Ph.D., MBA, or equivalent) in biotechnology, life sciences, business administration, or related field
  • Minimum of 3-5 years of experience in biotechnology or life sciences
  • Familiarity with the drug development process, particularly early-stage/preclinical development
  • Demonstrated experience working across multiple functions
  • Strong organizational skills with the ability to manage multiple workstreams simultaneously
  • Ability to synthesize complex scientific information in clear, actionable plans
  • Experience supporting or contributing to program or project planning
  • Excellent communication skills, both written and verbal
  • Detail-oriented, methodical, and proactive in identifying and solving problems
  • Comfortable operating in a fast-paced, evolving environment
  • Experience contributing to IND-enabling activities
  • Exposure to regulatory interactions or documentation
  • Proficiency in project management software

Expected salary range:

  • $185,000-215,000 annual base salary

Tenvie is proud to be an Equal Opportunity Employer. Our goal is to have a diverse workforce. We do not discriminate on the basis of race, age, color, religion, national origin, gender, sexual orientation, gender identity or expression, veteran status or disability or any other status protected under federal, state or local law. All employment is decided on the basis of qualifications, merit and business need.

 

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About the Company

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Tenvie Therapeutics