
201 - 500 employees
Founded 2016
🏥 Healthcare
🏭 Manufacturing
🧬 Biotechnology
Healthcare • Manufacturing • Biotechnology
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.
🔥 1 minute ago
🍂 Massachusetts – Remote
💵 $193k - $230k / year
⏰ Full Time
🟠 Senior
👨⚕️ Medical Director
🦅 H1B Visa Sponsor
👻 Ghost score 0%
Where this job comes from
Posted on Deciphera Pharmaceuticals's careers page, not through a job board
First seen by Remote Rocketship 1 minute ago

201 - 500 employees
Founded 2016
🏥 Healthcare
🏭 Manufacturing
🧬 Biotechnology
Healthcare • Manufacturing • Biotechnology
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.
• Lead ongoing clinical data review to support data quality, interpretation, and patient safety • Identify and escalate clinically relevant findings and partner with study teams to resolve data-related issues • Collaborate with Data Management and Clinical Operations on study implementation and EDC development • Contribute to and review clinical documents, including study protocols, investigator brochures, regulatory documents, and concept materials • Review and interpret clinical study data and outputs with Biostatistics, Pharmacovigilance, and other stakeholders • Represent Clinical Development on cross-functional study teams • Work closely with Medical Directors and functional partners • Prepare and present clinical data, study designs, and scientific information to study teams, investigator meetings, advisory boards, study committees, and other audiences • Perform other duties and responsibilities as assigned
• PhD or equivalent degree with 2+ years of relevant experience, or bachelor’s/master’s degree with 5+ years of relevant post-graduate experience • Pharmaceutical industry experience in clinical drug or biologics development • Experience as a Clinical Scientist or in a comparable clinical development role • Ability to work independently • Hands-on experience reviewing, analyzing, and interpreting clinical trial data • Strong cross-functional collaboration, organizational, communication, and presentation skills • Experience supporting Phase I–III clinical development programs preferred • Clinical development experience in oncology and/or neurology preferred • Rare disease experience preferred • Up to 20% business travel may be required
• Annual performance bonus • Long-term incentive plan • Comprehensive benefits package including medical, dental, and vision insurance • 401(k) retirement plan with company match • Generous parental leave and family planning benefits • Opportunities for personal and professional growth • Flexible hybrid or remote work arrangement within approved U.S. working locations
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