Business Services & Consulting • all cities, VT 47
Associate Director, Statistical Programming - Team Build (Remote) (47)
all cities, VT 47RemotePosted 2 hours ago
Business Services & Consulting
About the Role
A well-established, secure and commercially active biopharma is expanding its US statistical programming team. This is a project-level programming leadership role within a fully in-house function.
Responsibilities
Lead programming delivery across assigned oncology studies
Develop and validate SDTM, ADaM datasets and TFLs to submission standard
Support data delivery for CSR packages and regulatory submissions
Ensure alignment with CDISC standards and FDA/EMA requirements
Contribute to programming process development and standards
Experience Required
Bachelor's or Master's degree in a relevant discipline
Strong SAS programming experience within pharma or biopharma
Oncology experience required
Demonstrable experience working directly for a sponsor company
Solid working knowledge of CDISC standards (SDTM, ADaM)
East Coast based only
Compensation DOE - $170,000 - $220,000 base salary + benefits
A well-established, secure and commercially active biopharma is expanding its US statistical programming team. This is a project-level programming leadership role within a fully in-house function.
Responsibilities
Lead programming delivery across assigned oncology studies
Develop and validate SDTM, ADaM datasets and TFLs to submission standard
Support data delivery for CSR packages and regulatory submissions
Ensure alignment with CDISC standards and FDA/EMA requirements
Contribute to programming process development and standards
Experience Required
Bachelor's or Master's degree in a relevant discipline
Strong SAS programming experience within pharma or biopharma
Oncology experience required
Demonstrable experience working directly for a sponsor company
Solid working knowledge of CDISC standards (SDTM, ADaM)
East Coast based only
Compensation DOE - $170,000 - $220,000 base salary + benefits
What You'll Do
Lead programming delivery across assigned oncology studies
Develop and validate SDTM, ADaM datasets and TFLs to submission standard
Support data delivery for CSR packages and regulatory submissions
Ensure alignment with CDISC standards and FDA/EMA requirements
Contribute to programming process development and standards
Bachelor's or Master's degree in a relevant discipline
