Director – Program Management

🕒 August 21

🇺🇸 United States – Remote

💵 $250k - $295k / year

⏰ Full Time

🟠 Senior

📋 Program Manager

👻 Ghost score 2%

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Enliven Therapeutics

WebsiteLinkedInAll Job Openings

11 - 50 employees

🏥 Healthcare

💼 Consulting

🧬 Biotechnology

Healthcare • Consulting • Biotechnology

Enliven Therapeutics is a company dedicated to developing innovative solutions for cancer treatment. They focus on creating small molecule kinase inhibitors designed to improve efficacy, safety, and patient convenience. With programs targeting BCR-ABL, HER2, and additional pathways, Enliven Therapeutics aims to enhance the precision and selectivity of cancer therapeutics, combat resistance, and address brain metastases. The company prides itself on a team of experienced drug developers and aims to help cancer patients live longer and better lives.

📋 Description

• Serve as the operational leader of the cross-functional program team • Ensure alignment of strategy, timelines, resources, risks, and governance across Clinical Development, Regulatory, CMC, Biometrics, Medical Affairs, Commercial, Quality, and Corporate functions • Foster cross-functional alignment and facilitate operational excellence across Clinical Development, Regulatory Affairs, and CMC • Ensure timely delivery of program milestones • Develop and maintain integrated timelines mapping critical paths, regulatory filings, and clinical milestones • Drive accountability and communicate with the larger organization to support timely decision-making, risk management, and mitigations • Balance strategic thinking with disciplined execution to advance programs through development and regulatory approval • Implement program management best practices, tools, and governance processes • Drive continuous improvement initiatives across development operations • Standardize planning methodologies, reporting, and metrics • Champion operational discipline across cross-functional teams • Report to the Vice President, Program Management

🎯 Requirements

• Bachelor’s degree in Biological Sciences, Chemistry, or a related field required; Ph.D., MS, or MBA preferred • 12+ years in the biotech or pharmaceutical industry • Minimum 7+ years of experience in oncology or hematology drug development • Minimum 7+ years specifically in dedicated program or project management • Familiarity with tyrosine kinase inhibitors (TKIs) or hematologic malignancies highly desirable • Experience supporting NDA/BLA/MAA regulatory submissions strongly preferred • Experience within a clinical-stage biotechnology company preferred • Strong understanding of FDA/EMA regulations, CMC, and clinical trial phases • Advanced proficiency in Smartsheet or identical enterprise planning tools • PMP certification is a strong plus • Demonstrated ability to align cross-functional teams, resolve conflicts, and drive decision-making • Ability to work 40 hours per week; occasional evening, weekend, holiday, and on-call work may be required • Travel of around 30% may be expected • Successful completion of a background screen required for employment

🏖️ Benefits

• Bonus and equity may be provided • Full-time remote work • Equal opportunity employment • Background screen process for employment offers