Senior Manager, Statistical Programming/SAS Programming – San Francisco

TANNER & ASSOC INC; San Francisco (CA); On-site; USD 120,000 - 160,000; Full time

Job summary

A recruiting agency is seeking a Senior Manager for Statistical Programming in San Francisco. This role involves leading a programming team, managing statistical programming activities, and ensuring adherence to regulatory standards. The ideal candidate will have extensive experience in clinical programming, particularly within pharmaceuticals or CROs. Proficiency in SAS and a Master’s degree in a related field are required. Full relocation services within the US are offered.

Qualifications

• 8+ years in clinical programming with experience managing statistical programming for clinical trials.
• In-depth knowledge of CDISC standards (SDTM and ADaM).
• Significant knowledge of regulatory requirements and SOPs.

Responsibilities

• Manage statistical programming activities and deliverables.
• Lead programming team for electronic submission preparations.
• Ensure quality goals and timelines are met.

Skills

Project management

Statistical programming

SAS

VB Scripts

JAVA

Education

MS degree in Statistics, Computer Science, or related field

Tools

SAS

Job description

Senior Manager, Statistical Programming/SAS Programming – San Francisco

Tanner and Associates is recruiting a Senior Manager, Statistical Programming/SAS Programming for a large biotech company based in San Francisco. Full Relocation services provided within the US. Send a CV to [e-mail] .

Summary:

• The Senior Manager, Statistical Programming will be responsible for providing project management of statistical programming activities.
• They will deliver against the overall protocol timeline, cost, and quality goals through matrix communication with the study team and will be accountable for the provision of standard and non-standard datasets, tables, listings, and figures that are required for the study reports, submissions or publications.
• The Senior Manager, Statistical Programming will enforce standard of programming approaches and provide continuous improvement of processes and communicate effectively not only within the teams and functional lines but also with the external resources.
• In addition, they will lead the programming team to prepare for electronic submission activities including project plans, specifications, resource allocation, and deliverables in timely fashion.
• They will provide filing, approval and regulatory programming support for all aspects of a submission and contribute technical expertise to team deliverables and coach/train new programmer or processes related to team deliverables.
• They will also assess the impact of procedural or system changes, and develop/implement strategies to maintain consistency of programming.

Qualifications:

• MS degree and a minimum of 8 or more years experience in Statistics, Computer Science, or related field within a clinical programming organization, preferably within medium-large pharmaceuticals or CRO, 3 or more years experience in managing statistical programming aspects of clinical trials and direct reports, and NDA/BLA experiences a plus.
• Significant knowledge and experience with SOPs/Guidelines/System Life Cycle methodologies, ICH-GCP and applicable regulations as well as proven knowledge of regulatory document and reporting systems.
• Experience must include in-depth knowledge of CDISC in SDTM and ADaM, Metadata, and controlled terminologies.
• Proficiency in SAS and at least one programming environment such as VB Scripts and JAVA.

Please send a CV and contact information to Jake Tanner at [e-mail] . US candidates only please.