Deciphera Pharmaceuticals
201 - 500 employees
Founded 2016
🧬 Biotechnology
💊 Pharmaceuticals
Biotechnology • Pharmaceuticals
Deciphera Pharmaceuticals is a biotechnology company dedicated to defeating cancer by developing innovative kinase inhibitors to improve patient outcomes. The company focuses on designing switch-control kinase inhibitors to address mechanisms of tumor and drug resistance, aiming to enhance treatment responses for patients with cancer. Deciphera has a diverse pipeline of drug candidates, including ripretinib and vimseltinib, and is committed to making a significant impact on the lives of cancer patients. As of June 2024, Deciphera is a wholly-owned subsidiary of ONO Pharma and continues to work on improving human health through its scientific innovations and patient-centric approach.
Clinical Project Manager
🕒 March 11
🍂 Massachusetts – Remote
💵 $129k - $194k / year
⏰ Full Time
🟡 Mid-level
🟠 Senior
🏥 Clinical Operations
🦅 H1B Visa Sponsor
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Deciphera Pharmaceuticals
201 - 500 employees
Founded 2016
🧬 Biotechnology
💊 Pharmaceuticals
Biotechnology • Pharmaceuticals
Deciphera Pharmaceuticals is a biotechnology company dedicated to defeating cancer by developing innovative kinase inhibitors to improve patient outcomes. The company focuses on designing switch-control kinase inhibitors to address mechanisms of tumor and drug resistance, aiming to enhance treatment responses for patients with cancer. Deciphera has a diverse pipeline of drug candidates, including ripretinib and vimseltinib, and is committed to making a significant impact on the lives of cancer patients. As of June 2024, Deciphera is a wholly-owned subsidiary of ONO Pharma and continues to work on improving human health through its scientific innovations and patient-centric approach.
📋 Description
• Support cross-functional study execution teams to drive successful clinical trial delivery • Provide strategic guidance and oversight to study teams, proactively resolving operational challenges and risks • Manage study timelines, resources, and deliverables to ensure trials meet quality, cost, and schedule expectations • Oversee CROs and external vendors to ensure performance aligns with contractual and operational requirements • Support study feasibility, including patient enrollment strategies, site selection, and data collection planning • Contribute to protocol development and ensure study execution aligns with program objectives • Implement risk mitigation strategies to support successful trial outcomes
🎯 Requirements
• Bachelor’s or Master’s degree with 5+ years of clinical research experience, including clinical trial management • Demonstrated experience managing and executing clinical studies • Strong knowledge of regulatory requirements, including ICH guidelines and GCP • Experience overseeing CROs and external vendors • Proven ability to lead matrixed, cross-functional teams • Excellent communication, presentation, and stakeholder management skills • Experience with late-phase clinical trials (Phase 2b or Phase 3) • Experience managing global clinical trials and supporting regional regulatory submissions.
🏖️ Benefits
• Competitive salary and annual bonus. • Comprehensive benefits package including medical, dental, vision insurance, 401(k) retirement plan with company match, and more. • Generous parental leave and family planning benefits. • Outstanding culture and opportunities for personal and professional growth.
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