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Enliven Therapeutics

Vice President, Supply Chain

Vice President, Supply Chain Location: Remote, USA Status: Full-Time Exempt Department ... CMC Enliven Therapeutics is a clinical-stage biopharmaceutical company focused on the discovery and ...

City Therapeutics

VP, Controller

Cambridge, MA · On-site

$270K - $325K/yr

VP Controller Company Overview City Therapeutics is biopharmaceutical company leading the future of ... Partner with business colleagues including Clinical Operations, CMC, and Program Management to ...

AskBio

VP, GDNF Clinical Development

... CMC. They will be responsible for establishing and overseeing global clinical development ... The VP, GDNF Clinical Development will partner with AskBio's Safety and Pharmacovigilance teams to ...

City Therapeutics

VP, Controller

Cambridge, MA · On-site

$270K - $325K/yr

VP Controller Company Overview City Therapeutics is biopharmaceutical company leading the future of ... Partner with business colleagues including Clinical Operations, CMC, and Program Management to ...

AskBio

VP, GDNF Clinical Development

Durham, NC

... CMC. They will be responsible for establishing and overseeing global clinical development ... The VP, GDNF Clinical Development will partner with AskBio's Safety and Pharmacovigilance teams to ...

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Vp Cmc information

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How much do vp cmc jobs pay per year?

As of Sep 14, 2026, the average yearly pay for vp cmc in the United States is $157,532.00, according to ZipRecruiter salary data. Most workers in this role earn between $115,000.00 and $190,000.00 per year, depending on experience, location, and employer.

What is a VP CMC?

A VP CMC (Vice President of Chemistry, Manufacturing, and Controls) is a senior executive responsible for overseeing all aspects of drug development related to chemistry, manufacturing processes, and quality controls. This role typically exists in pharmaceutical or biotechnology companies and ensures that products are developed, manufactured, and controlled according to regulatory standards. The VP CMC collaborates with research, regulatory, and commercial teams to ensure efficient and compliant product development from early research through commercialization. They are also responsible for managing teams, budgets, and timelines to meet critical milestones.

What are the typical challenges a VP CMC faces when scaling up manufacturing for clinical trials and commercial launch?

A VP of CMC (Chemistry, Manufacturing, and Controls) often encounters challenges in scaling up manufacturing processes, including ensuring consistent product quality, meeting strict regulatory requirements, and managing timelines across multiple stakeholders. Coordinating between R&D, manufacturing, and quality teams is crucial to address technical hurdles and maintain compliance. Additionally, adapting to evolving regulations and managing supply chain complexities are key responsibilities, especially when progressing from clinical trials to commercial production.

What are the key skills and qualifications needed to thrive as a VP CMC, and why are they important?

To thrive as a VP CMC, you need deep expertise in pharmaceutical development, regulatory compliance, and process optimization, typically supported by an advanced degree in chemistry, chemical engineering, or a related field. Familiarity with regulatory submission systems, quality management platforms, and CMC documentation tools is essential. Leadership, strategic thinking, and excellent communication are critical soft skills for guiding cross-functional teams and aligning stakeholders. These skills ensure efficient drug development, regulatory approval, and successful product launches in a highly regulated industry.

What is the difference between Vp Cmc vs Regulatory Affairs Manager?

AspectVp CmcRegulatory Affairs Manager
CredentialsAdvanced degrees in life sciences, experience in CMC developmentBachelor's or Master's in life sciences, regulatory certifications
Work EnvironmentStrategic leadership in R&D and manufacturingRegulatory compliance, documentation, and submissions
Industry UsagePharmaceutical and biotech companies, overseeing CMC activitiesRegulatory agencies, pharmaceutical companies, ensuring compliance

The Vp Cmc focuses on overseeing chemistry, manufacturing, and controls (CMC) processes at a strategic level, ensuring product quality and compliance. Regulatory Affairs Managers handle regulatory submissions and compliance activities. While both roles require industry knowledge, Vp Cmc roles are more senior and strategic, whereas Regulatory Affairs Managers focus on regulatory documentation and compliance tasks.

What cities are hiring for Vp Cmc jobs?

Cities with the most Vp Cmc job openings:

What are the most commonly searched types of Cmc jobs?

The most popular types of Cmc jobs are:

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States with the most job openings for Vp Cmc jobs include:

What are popular job titles related to Vp Cmc jobs?

For Vp Cmc jobs, the most frequently searched job titles are:

Vp Cmc jobs near you
Infographic showing various Vp Cmc job openings in the United States as of September 2026, with employment types broken down into 97% Full Time, 2% Part Time, and 1% Contract. Highlights an 75% Physical, 4% Hybrid, and 21% Remote job distribution, with an average salary of $157,532 per year, or $75.7 per hour.

Vice President, Supply Chain

Remote

Enliven Therapeutics
Biotechnology Research and Development • 11 - 50 employees
Learn more about Enliven Therapeuticsexternal

Full-time

Posted 23 days ago

Job description

Job Type
Full-time
Description
Role Title: Vice President, Supply Chain
Location: Remote, USA
Status: Full-Time Exempt
Department: CMC
Enliven Therapeutics is a clinical-stage biopharmaceutical company focused on the discovery and development of small molecule inhibitors to help people with cancer not only live longer, but live better. The Company aims to address existing and emerging unmet needs with a precision medicine approach that improves survival and enhances overall well-being. Its discovery process combines deep insights in clinically validated biological targets and differentiated chemistry with the goal of designing therapies for unmet needs.
Role Summary
The Vice President, Supply Chain will own Enliven's global supply chain strategy while preparing the company for late-stage development, regulatory approval, and commercial supply.
This leader will ensure uninterrupted supply of investigational product across Enliven's clinical programs and coordinate closely with CMC, Clinical Operations, Quality, Regulatory, Commercial, Finance, and other functions. The role requires someone who can set strategy while remaining actively involved in forecasting, planning, logistics, vendor oversight, risk management, and issue resolution.
A key mandate is to anticipate potential supply gaps and ensure that manufacturing, packaging, labeling, release, inventory, or logistics issues do not disrupt clinical development or future commercial supply. The successful candidate will bring direct experience moving products from clinical development into commercial operations and supporting at least one pharmaceutical product launch.
Key Responsibilities
Clinical Supply Leadership
  • Lead global clinical supply strategy and execution across Enliven's portfolio, ensuring uninterrupted supply for current and future clinical trials.
  • Translate clinical protocols, enrollment assumptions, development plans, and manufacturing schedules into demand forecasts, supply plans, inventory strategies, and budgets.
  • Provide hands-on oversight of forecasting, production planning, packaging, labeling, distribution, inventory management, logistics, returns, reconciliation, and destruction.
  • Coordinate internally across Clinical Operations, CMC, Quality, and Regulatory to align manufacturing, release, packaging, and distribution activities with program and study timelines.
  • Oversee global logistics, including import/export activities, customs documentation, depot strategy, and country-specific labeling and distribution requirements.
  • Establish appropriate inventory and safety-stock strategies, balancing continuity of supply, shelf life, cost, and program risk.
  • Proactively identify potential supply gaps, capacity constraints, and logistics challenges; develop scenarios, contingencies, and mitigation plans.
  • Lead cross-functional resolution of supply disruptions and other unplanned events affecting clinical timelines or patient supply.
  • Oversee IRT-related supply strategy and execution and comparator sourcing, as applicable.
  • Support relevant clinical and regulatory documentation, submissions, inspections, and audit-readiness activities.

Late-Stage and Commercial Supply Readiness
  • Develop and execute the roadmap for transitioning Enliven from a clinical-stage supply model to a scalable commercial supply chain.
  • Establish fit-for-purpose processes, systems, governance, and external partnerships for late-stage development, launch, and ongoing commercial supply.
  • Lead commercial supply and launch-readiness planning, including demand and supply planning, inventory strategy, packaging and labeling, serialization, distribution, logistics, 3PL strategy, and product traceability.
  • Partner with Commercial and Finance on integrated forecasting, demand planning, and S&OP/IBP capabilities appropriate to the company's stage.
  • Ensure commercial supply requirements are incorporated early into manufacturing, packaging, regulatory, distribution, and lifecycle strategies.
  • Develop launch scenarios and contingency plans addressing regulatory timing, demand uncertainty, manufacturing capacity, release timing, inventory, and market uptake.
  • Help ensure a seamless transition from clinical to commercial supply without operational or logistical gaps.

External Supply Network and Operational Execution
  • Oversee Enliven's external supply network, including CMOs/CDMOs, packaging and labeling providers, depots, logistics providers, and 3PLs.
  • Lead vendor evaluation, selection, contracting, onboarding, governance, and performance management, including RFPs and SOWs.
  • Partner with CMC and Quality to ensure external partners can meet evolving clinical, registrational, and commercial requirements.
  • Develop sourcing, contracting, capacity-planning, and business-continuity strategies for critical supply activities.
  • Maintain clear visibility into inventory, supply status, assumptions, risks, budgets, and key decisions, providing timely updates to senior leadership.
  • Develop scalable SOPs, planning processes, systems, and performance metrics that improve supply visibility, reliability, and execution.
  • Serve as the supply-chain subject-matter expert during audits and inspections, as appropriate.

Cross-Functional and Hands-On Leadership
  • Serve as Enliven's senior supply-chain leader while remaining actively engaged in day-to-day planning, execution, problem-solving, and decision-making.
  • Coordinate closely with CMC, Clinical Operations, Quality, Regulatory, Commercial, Finance, Legal, and other departments to maintain alignment and resolve dependencies.
  • Represent Supply Chain and, when appropriate, CMC or Technical Operations in program teams, governance forums, and leadership discussions.
  • Clearly communicate supply strategy, readiness, risks, tradeoffs, and investment requirements to executive leadership.
  • Provide practical direction and support to supply-chain team members while fostering accountability, collaboration, and proactive risk management.

Requirements
Required
  • Bachelor's degree in supply chain, engineering, life sciences, business, or a related field; advanced degree preferred.
  • Approximately 15 or more years of progressively responsible pharmaceutical or biotechnology supply-chain experience.
  • Deep, hands-on experience leading global clinical supply, including forecasting, inventory management, packaging and labeling, distribution, logistics, and external-partner oversight.
  • Experience leading supply chain for pivotal/Phase 3 clinical development and transitioning products from clinical-stage operations through commercial readiness.
  • Firsthand experience establishing commercial supply-chain capabilities and playing a supply chain leadership role in at least one pharmaceutical product launch, including supporting NDA readiness and pre-approval inspections.
  • Strong knowledge of clinical and commercial supply requirements, including demand planning, inventory strategy, packaging and labeling, serialization, distribution, 3PL management, and product traceability.
  • Experience managing CMOs/CDMOs and other outsourced supply partners within a virtual or highly outsourced biotechnology model.
  • Experience building and leading supply chain organizations, including planning internal staffing, consultant support and outsourced capabilities.
  • Strong understanding of GMP, GDP, and applicable global clinical-supply requirements.
  • Experience leading or materially participating in ERP/planning/inventory management/supply visibility systems implementation.
  • Demonstrated ability to anticipate supply gaps, build practical contingency plans, and resolve disruptions quickly.
  • Ability to work effectively at both strategic and tactical levels in a small or mid-sized biotechnology company.
  • Strong cross-functional leadership, communication, financial judgment, negotiation, and problem-solving skills.
  • Ability to manage multiple priorities and make sound decisions in a fast-paced, evolving environment.

Preferred
  • Experience building the clinical and commercial supply capabilities for an emerging biotechnology company's first commercial product.
  • Experience with small-molecule pharmaceutical products and outsourced global manufacturing and distribution networks.
  • Experience supporting global, multi-region clinical trials.
  • Experience supporting U.S. and international product launches.
  • Working knowledge of IRT systems.

This is a full-time remote position (40 hours/week). Occasional evening, weekend, holiday, and on-call work may be required as job duties demand. Travel of around 15% may be expected for this role.
The annual salary range Enliven reasonably and in good faith expects to pay for this position at the time of this posting is $300k - $340k. The actual salary offered will be determined based on factors such as experience, qualifications, skills and expertise, geographic location, and other job-related factors permitted by law. Benefits are included and other incentives such as bonus and equity may be provided. This range is subject to change based on business needs, job scope changes, market conditions, and individual qualifications. Employees and applicants may request the pay range for their position or for a position to which they are applying.
Enliven Therapeutics is proud to be an equal opportunity employer. All employment offers are contingent upon the applicant successfully completing a background screen.
Notice to agencies: Our in-house Talent Acquisition Team manages all employment opportunities at Enliven. Agencies and independent recruiters must be approved as a vendor by our HR team. To protect the interests of all parties, Enliven will not accept unsolicited resumes, profiles, or biographies. Any unsolicited submissions will be considered referrals and become the property of Enliven. Contacting hiring managers, executives, or any member of the HR team will not influence vendor approval and is strongly discouraged. Repeated outreach may impact future consideration.

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