Associate Director, Clinical Science

🔥 0 minutes ago

🍂 Massachusetts – Remote

🍂 Massachusetts – Remote

💵 $171k - $236k / year

⏰ Full Time

🟠 Senior

👨‍⚕️ Medical Director

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

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Deciphera Pharmaceuticals

WebsiteLinkedInAll Job Openings

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.

📋 Description

• Contribute to execution of clinical development plans for candidate drug products with Project Leaders and Medical Directors • Operationalize clinical studies and monitor data in real time to ensure study integrity • Proactively identify and escalate issues in trial conduct • Perform high-level clinical data review for quality and patient safety • Collaborate with data management, clinical operations, and medical monitors on clinical data review • Communicate and escalate issues internally and to investigators • Collaborate on EDC builds according to protocol specifications • Author and review clinical documents, including concept sheets/decks, clinical study protocols, investigator brochures, and regulatory documents • Generate clinical outputs and provide initial interpretation for internal purposes and external interactions • Review Tables/Listings/Figures and SAP updates with Biostatistics, Pharmacovigilance, and other stakeholders • Participate in regular study team meetings representing clinical development • Organize and present data, study designs, and other information to advisory boards, investigator meetings, site interactions, study committees, and internal and external audiences • Perform other duties and responsibilities as assigned

🎯 Requirements

• PhD or equivalent plus 5+ years of experience, or bachelor/master’s degree plus 10+ years of postgraduation experience • Pharmaceutical industry experience in clinical drug/biologics development and associated regulatory processes • Strong organizational skills for data collection and documentation supporting clinical trial analysis and interpretation • Ability to interact effectively with internal team members and external partners • Experience with clinical data analysis • Ability to influence decision-making within a multidisciplinary team in areas of expertise • Excellent communication and presentation skills • Up to 20% business travel may be required • Experience across Phase I–III drug development trials preferred • Product development experience in Hematology-Oncology and/or rare disease preferred

🏖️ Benefits

• Equity-based compensation • Medical insurance • Dental insurance • Vision insurance • 401(k) retirement plan with company match • Life insurance • Flexible spending account for health care and/or dependent care • Annual performance bonus • Long-term incentive plan • Generous parental leave • Family planning benefits • Opportunities for personal and professional growth