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Responsibilities:
- Lead the development of statistical sections of clinical study protocols.
- Provide strategic input to optimize trial designs.
- Oversee CRO statistical activities.
Competencies:
- Adaptability/Flexibility to changes in job demands.
- Communication and Teamwork with internal and external stakeholders.
- Effective Planning and discipline in approaches.
Qualifications:
- Minimum of MS required (Ph.D. preferred) in Statistics, Biostatistics, or other related fields.
- Oncology experience is strongly preferred: familiar with oncology drug development.
- Must have hands on experiences with SAS programming in clinical studies.
Additional Information:
- Nuvalent is committed to fair and equitable compensation practices.
- Offers a comprehensive benefit package.
- Including medical, dental, and vision insurance, 401(k) retirement savings plan, generous paid time off.
Nuvalent
Nuvalent is working to create selective medicines designed with the goal to address the needs of patients with cancer. Nuvalent is an early-stage company, bringing together experienced scientists and industry veterans with a proven track record in drug discovery, oncology drug development, and company building.