About Outpace BioOutpace Bio is pioneering the future of cell therapy for solid tumors by harnessing AI-powered protein design. Their mission is to program immune cells for enhanced function inside patients, overcoming key barriers such as poor tumor access, weak survival, antigen escape, and dose-related toxicity. The team works across computational protein design, synthetic biology, and immunology to develop programmed T cell therapies.About the roleOutpace Bio is seeking a highly motivated and experienced Clinical Scientist to lead cross-functional teams designing and advancing programmed T cell therapies into the clinic. Reporting to the Senior Medical Director, the Clinical Scientist will contribute to the scientific, clinical, and operational scope of clinical development programs with an emphasis on study and program-specific activities.Key Responsibilities (position responsibilities may include, but are not limited to):Serve as study clinical scientist on oncology cell therapy trials; partner closely with the Senior Medical Director in execution of the clinical development strategy for assigned asset(s).Actively participate in study start-up activities, asset team meetings, safety monitoring committees, and coordinate patient enrollment and dosing with product manufacturing/delivery managed by technical operations and clinical operations.Conduct review of emerging clinical and medical data to ensure quality data; review and query data; present and discuss relevant data to appropriate teams and stakeholders.Collaborate on preparation and review of clinical protocols and amendments; support development of study and regulatory documents including informed consent forms, investigator brochures, statistical analysis plans, regulatory documents, annual reports, and clinical study reports (CSRs).Support clinical development activities during implementation of the clinical database with a CRO.Review risks, query resolution, and protocol deviations; support development of publications, abstracts, and presentations.Develop effective collaborations with internal and external partners, including cross-functional team members, consultants, asset team leaders, and clinical trial site staff.Serve as technical resource for clinical issues raised by internal and external collaborators, investigators, consultants, and contractors.Participate in project teams to implement clinical development and contribute to key milestones (e.g., start-up and delivery of POC trials).Required Qualifications:Bachelor's degree or advanced degree (MSc, PharmD, MD, PhD) in Life Sciences, Pharmacology, or related field.Minimum of 3 years’ experience conducting/supporting oncology/hematology clinical studies; experience in early phase development and/or cell therapy preferred.Excellent written and verbal communication skills.Experience interpreting clinical research results including safety and efficacy; familiarity with statistical principles desirable.Ability to think strategically and tactically with interest in clinical research and drug development focused on delivering results and driving innovation.Ability to adapt and problem-solve in an agile, fast-paced, start-up, team-based matrix environment; able to function independently as appropriate; flexible to accommodate changes in team and project needs.Ability to handle multiple projects at a time with strong attention to detail while understanding the higher-level strategy.Passion for developing complex, innovative medicines for solid tumors.LocationRemote — candidates based in the following states will be considered to align with company operations: CA, OR, or WA.Total RewardsFull-time employees and their eligible dependents may enroll in medical, dental, vision, life insurance, disability, flexible spending account, health savings account, commuter benefits, legal benefits, and a 401k plan with an employer match. Employees may also receive stock option grants and a performance bonus. Benefits include flexible PTO, paid sick leave (per local requirements), fifteen paid holidays plus a winter shutdown, and a generous paid parental leave policy for all regular full-time employees.Diversity & Equal OpportunityOutpace Bio is committed to a diverse workforce and makes employment decisions without discrimination based on protected characteristics.Work AuthorizationApplicants must be authorized to work in the United States; if legally authorized now or in the future without sponsorship, they are encouraged to apply.
