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Position Overview:
- Provide planning and execution of SAS programming for clinical trial analysis and reporting.
- Ensure submission-ready data packages per CDISC standards and regulatory guidance.
Responsibilities:
- Lead statistical programming for 1-2 assigned studies, developing specifications and overseeing CDISC datasets.
- Provide hands-on SAS support for key analyses and ad hoc requests.
- Manage CRO activities and mentor junior team members.
Qualifications:
- Master's degree in Statistics, Computer Science, or related field with 6+ years pharma experience.
- Solid knowledge of clinical trials, regulatory requirements, and CDISC standards.
- Strong SAS programming skills and prior NDA submission experience preferred.
Why Join Us:
- Opportunity to develop best-in-class targeted cancer therapies.
- Collaborative environment with experienced leadership.
- Comprehensive benefits including medical, 401(k), and paid parental leave.
Immunome
Immunome is a clinical-stage targeted oncology company developing first-in-class and best-in-class cancer therapies. The company offers an innovative, collaborative environment where employees are empowered to do their best work.