Statistical Programmer

The Lotus Group LLC; Massachusetts; Hybrid; USD 170,000 - 230,000; Full time

Job summary

The Lotus Group LLC seeks an Associate Director Statistical Programmer on a hybrid basis in Massachusetts. This leadership role will drive the statistical programming strategy across a late-stage, multi-study portfolio while staying hands-on with technical decisions and deliverables.

You will mentor programming resources, collaborating closely with Biostatistics, Data Management, Clinical Operations, and Regulatory to ensure high-quality outputs for submissions and regulatory packages.

Qualifications

• 8+ years of Pharma Clinical SAS experience.
• Experience leading programming for an entire clinical-development program.
• Prior programming leadership or management experience with internal staff, FSPs, and/or vendors.
• Expertise in SAS, including Base, Macro, STAT, Graph, and SQL.
• Strong experience with CDISC standards: SDTM, ADaM, and Define-XML.
• Hands-on R programming experience supporting clinical-trial analysis, reporting, and/or regulatory submissions.
• Experience supporting complex, global, late-stage, multi-study, high-volume, or submission-oriented programs.
• A collaborative leadership style with the ability to influence senior cross-functional stakeholders.

Responsibilities

• Lead program-level statistical programming strategy for a late-stage portfolio.
• Mentor and manage programming resources across internal staff and vendors.
• Partner with Biostatistics, Data Management, Clinical Operations, and Regulatory to ensure quality deliverables.
• Oversee hands-on programming work and technical decision-making for complex analyses.

Skills

Program leadership

SAS programming

R programming

Cross-functional collaboration

Mentoring

Regulatory submissions

Tools

SAS

R

Define-XML

Job description

Associate Director Statistical Programmer- hybrid in MA

Midsize biotech client is looking to hire an AD SAS Programmer for a highly visible, complex clinical-development program. Lead program-level statistical programming strategy while remaining hands-on with technical decisions, deliverables, and problem-solving. Will manage and mentor programming resources, partner closely with Biostatistics, Clinical Data Management, Clinical Operations, and Regulatory, and help drive high-quality outputs across a late-stage, multi-study development portfolio.

Requirements:

• 8+ years of Pharma Clinical SAS experience
• Experience leading programming for an entire clinical-development program
• Prior programming leadership or management experience with internal staff, FSPs, and/or vendors
• Expertise in SAS, including Base, Macro, STAT, Graph, and SQL.
• Strong experience with CDISC standards: SDTM, ADaM, and Define-XML.
• Hands-on R programming experience supporting clinical-trial analysis, reporting, and/or regulatory submissions.
• Experience supporting complex, global, late-stage, multi-study, high-volume, or submission-oriented programs.
• A collaborative leadership style with the ability to influence senior cross-functional stakeholders.