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Join to apply for the VP, Clinical Development / CMO / CDO role at Autonomy Bio

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We are an early-stage biotech company developing drugs with the goal of reducing multi-morbidity and earning an indication for aging, as opposed to the treatment of specific diseases. Our ultimate mission is to establish aging as a therapeutic area and empower humans with more time with loved ones and autonomy over their health. This is a new paradigm focused on keeping healthy people healthy as opposed to treating individual diseases after they occur.

Key Responsibilities

• Design & Own the Clinical Roadmap : Develop and own the integrated clinical plan for our lead program and broader pipeline.
• Regulatory Coordination : Work closely with our regulatory lead to strategize and execute a regulatory strategy for aging therapies. Lead all major regulatory interactions - briefing packages, meeting prep, post-meeting strategies.
• Program Management : Track milestones and dependencies to keep trials on schedule and under budget.
• Develop and Validate Novel Aging Endpoints : Collaborate with scientific and regulatory stakeholders to define, validate, and advocate for new clinical endpoints that capture aging-related healthspan improvements.
• Innovate in Trial Design : Incorporate decentralized trials, adaptive protocols, AI-driven endpoints, and real-world data to cut costs, accelerate timelines, and maximize impact.
• Build the Team : Hire, mentor, and inspire a world-class clinical and regulatory team, with no ego and a high bar for performance, creativity, and mission alignment.
• Drive Quality and Compliance : Develop and institutionalize a biotech-focused QMS.

Measures of Success

Within the First 3–6 Months, You Will Have :

• Delivered a Briefing Package for our second FDA Type C Meeting, integrating inputs from clinical ops, regulatory, CMC, and external experts.
• Finalized Phase 1 Study Synopses (focusing on fixed-dose combination PK / safety), incorporating FDA feedback and bridging strategies for a 505(b)(2) or similar pathway.
• Mapped a Multi-Country Clinical Development Plan that accounts for differing regulatory views on aging endpoints, accelerating potential global acceptance.
• Built Core Clinical Team & Processes : Hired 2–3 specialized staff (trial ops, regulatory managers), instituted a biotech-specific QMS, and established training protocols.
• Established Integration with AI / Data Leads to ensure Phase 1 readouts can be tracked in real-time, especially for unique combination PK / PD data.

Within the First Year, You Will Have :

• Navigated Key FDA Milestones such that the IND for AUTO-1 is approved on schedule; shaped a feasible Phase 3 design aligned with FDA insights on aging endpoints.
• Executed a Timely Phase 1 Readout that validates combination safety data, enabling immediate pivot or progression to Phase 3.
• Formed External Alliances & Collaborations with academic sites and KOLs in geriatric cardiology / metabolism, possibly advancing major pharma partnership opportunities.
• Expanded the Clinical Organization to manage parallel pipeline programs, hiring additional senior managers in clinical development, trial ops, and regulatory.
• Implemented Continuous Innovation in Trial Design (digital endpoints, remote data capture, adaptive protocols) to reduce cost per patient and overall trial duration.
• Strong Ownership & Leadership : Proven ability to “run the show” for clinical development, orchestrating cross-functional teams with autonomy and accountability.
• Hiring & Talent Magnet : Deep network in clinical development; adept at building and scaling teams from scratch, especially in early-stage biotech.
• Creative Problem-Solving & Cost Reduction : Track record of innovating clinical trial designs (e.g., decentralized, AI-driven) to reduce timeline and budget by 20–30%.
• Regulatory & Geriatric Endpoint Expertise : Skilled at navigating FDA processes for combination products and demonstrating synergy; familiarity with unique geriatric endpoints such as intrinsic capacity or multi-factor biomarkers.
• Rigor & Detail Orientation : Highly meticulous with briefing materials, risk assessments, and scenario planning; understands how to proactively manage FDA queries.
• Resilience & Toughness : Comfortable in fast-paced, high-stakes environments. Willing to stand firm under pressure from executives, investors, and regulators alike.

Preferred Qualifications

• 3+ Years of Senior Clinical Development Experience in biotech, pharma, or a related field, ideally with at least 2 years in a startup environment.
• Experience with Long-Duration Studies : Experience handling 5–7-year follow-up trials or outcomes-based studies with novel endpoints.
• Global Regulatory Acumen : Experience aligning clinical endpoints across multiple regulatory bodies and geographies.
• Advanced Degree (MD or Equivalent) in a related Life Sciences field preferred.
• Experience in Therapeutic Areas Without Established Endpoints : Comfortable designing and validating new clinical endpoints where regulatory precedents are limited or evolving.
• Experience in the therapeutic areas : neurodegeneration, cardiometabolism, rare diseases or vaccines.

Seniority level

Seniority level

Executive

Employment type

Employment type

Full-time

Job function

Job function

Research, Analyst, and Information Technology

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