Director, Clinical Scientist

🔥 6 minutes ago

🇺🇸 United States – Remote

💵 $192k - $239k / year

⏰ Full Time

🔴 Lead

👨‍⚕️ Medical Director

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Summit Therapeutics, Inc.

WebsiteLinkedInAll Job Openings

201 - 500 employees

Founded 2003

🏥 Healthcare

💼 Consulting

📣 Marketing

🔥 Funding within the last year

💰 $500M Post-IPO Equity - Summit Therapeutics on 2025-10

Healthcare • Consulting • Marketing

Summit Therapeutics, Inc. is a biopharmaceutical oncology company focused on the discovery, development, and commercialization of novel medicinal therapies to improve quality and duration of life for patients with serious unmet medical needs. The company is advancing ivonescimab (SMT112), a novel bispecific antibody targeting PD-1 and VEGF, through multiple Phase 3 clinical trials for non-small cell lung cancer and other solid tumors under license from Akeso. Summit emphasizes clinical development, regulatory filing strategies, and potential commercialization in its licensed territories while promoting patient- and caregiver-friendly treatment options.

📋 Description

• Lead/contribute to study design and amendments with internal and external scientific stakeholders • Collaborate with MD, regulatory, and internal partners on protocols, amendments, regulatory filings, and documentation • Develop and implement data quality plans and lead medical data review and safety trend analysis • Serve as point of contact for clinical inquiries from CRO medical monitors and stakeholders • Develop clinical presentation slides and communications for meetings, site visits, training, newsletters, and study sites • Develop and maintain study startup documents and resources, including ICF, Lab Manual, EDC, and Safety Monitoring Plan • Participate in safety meetings and review potential safety events • Develop communications strategies for studies, including KOL interactions, advisory boards, medical meetings, publications, and events • Write or review abstracts, posters, scientific meeting content, presentations, and publicly distributed materials • Coordinate submissions to scientific meetings and appropriate venues • Write clinical science sections of meeting packages and support clinical documentation for regulatory submissions • 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 • Variable compensation may be included in the total compensation package • Equal Opportunity Employer