
Senior Program Director – Regulatory and Clinical Development
Akero Therapeutics
full-time
Posted on:
Location Type: Remote
Location: United States
Visit company websiteExplore more
Salary
💰 $181,670 - $317,920 per year
Job Level
Tech Stack
About the role
- Own and execute program and portfolio management strategy across Akero’s development organization
- Serve as primary cross functional integrator, ensuring alignment between strategy, execution, governance and decision making across programs.
- Partner with Development Therapeutic Area VPs and senior leaders to advance strategic priorities and ensure clear accountability, ownership, and decision rights.
- Design, implement, and run Akero’s development governance model in alignment with the parent organization.
- Establish and maintain decision-making frameworks, escalation pathways, and executive visibility into risks, trade-offs, dependencies, and outcomes.
- Lead Akero Development governance meetings and ensure consistent alignment with parent company processes and expectations.
- Collaborate with TechOps (CMC) to develop, gain approval, and execute on the project strategy in alignment with parent company
- Lead cross-functional alignment across departments, proactively identifying and resolving risks, conflicts, and misalignments.
- Oversee program timelines, integrated development plans, and delivery of key milestones across the portfolio.
- Manage trade-offs and dependencies, escalating issues to senior leadership as needed to maintain progress and alignment.
- Identify gaps in capabilities, training, and processes (e.g., GCP training), and partner with Quality to support compliance activities as needed.
- Establish scalable systems, templates, tools, and best practices for program and portfolio management.
- Own portfolio-level risk and issue management, ensuring mitigation strategies are proactively developed and executed.
- Monitor program performance and intervene as needed to keep programs on track.
- Partner with Finance and leadership on development budgets, forecasting, and resource allocation across the portfolio.
- Build, mentor, and develop program management talent.
- Organize and deploy project management support across functional areas and programs.
- Foster a high-performing, accountable, and collaborative program management culture.
Requirements
- Minimum of a bachelor's degree required, advanced degree (master's or PhD preferred), preferably within a scientific discipline or other related fields.
- 15+ years of proven experience in biotech / pharma portfolio and project management at a strategic and operational level
- Preferred experience working with Phase III trials for liver indications
- Demonstrated ability to lead transformation initiatives and drive organizational change.
- Strong financial acumen and experience with budget ownership and planning.
- Expertise in governance frameworks and decision-making processes.
- Track record of building and developing high-performing teams.
- Excellent communication, stakeholder management, and cross-functional leadership skills.
- Knowledgeable about lab-engineered analogs highly preferred
Benefits
- medical, dental and vision coverage
- life insurance
- disability insurance
- 401(k) savings plan
- flexible spending accounts
- employee assistance program
- tuition reimbursement program
- group legal
- critical illness
- identity theft protection
- pet insurance
- auto/home insurance
- sick time policy
- flexible vacation policy
- parental leave policy
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
program managementportfolio managementgovernance frameworksbudget planningrisk managementproject strategyPhase III trialscompliance activitiesdecision-making processesfinancial acumen
Soft Skills
leadershipstakeholder managementcross-functional collaborationorganizational changementoringcommunicationproblem-solvingaccountabilityteam developmenthigh-performing culture