Director, Clinical Scientist

🕒 October 14

🇺🇸 United States – Remote

💵 $192k - $239k / year

⏰ Full Time

🔴 Lead

👨‍⚕️ Medical Director

👻 Ghost score 23%

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Summit Therapeutics, Inc.

WebsiteLinkedInAll Job Openings

51 - 200 employees

Founded 2003

🏥 Healthcare

🧬 Biotechnology

💊 Pharmaceuticals

Healthcare • Biotechnology • Pharmaceuticals

Summit Therapeutics, Inc. is a biopharmaceutical oncology company focused on the discovery, development, and commercialization of innovative medicinal therapies aimed at improving quality of life for oncology patients. The company is particularly committed to addressing serious unmet medical needs through its lead investigational therapy, ivonescimab, a novel bispecific antibody designed to target both PD-1 and VEGF. Summit’s initiatives include ongoing Phase III clinical trials to evaluate ivonescimab's effectiveness in treating non-small cell lung cancer, highlighting their dedication to patient-centered care and technological advancement in the field of oncology.

📋 Description

• Lead or contribute to clinical study design and amendments with internal and external scientific stakeholders • Collaborate with MD, regulatory, clinical operations, data management, CRO, and other partners on protocols, regulatory filings, data quality, and safety analysis • Serve as point of contact for clinical inquiries from CRO medical monitors and stakeholders • Develop clinical presentation slides, study materials, training resources, and site communications • Partner on study start-up documents and resources including ICF, Lab Manual, EDC, and Safety Monitoring Plan • Participate in safety meetings and track, analyze, and review potential safety events • Develop and implement communications strategies including KOL interactions, advisory boards, meetings, congresses, publications, and other events • Write or review abstracts, posters, presentations, and scientific meeting materials • Coordinate submissions to scientific meetings and appropriate venues • Write clinical science sections of meeting packages and support regulatory documentation • Perform other duties as assigned

🎯 Requirements

• MS (or equivalent) required; PhD, PharmD, or MD preferred • Minimum of 5+ years overall related experience with PhD or like degree • Minimum of 2+ years’ experience in conducting / supporting oncology/hematology clinical studies • Excellent written and verbal communication skills • Expertise in interpreting immunology/immuno-oncology translational data in addition to clinical data

🏖️ Benefits

• Potential bonus • Stock • Benefits • Other applicable variable compensation

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