Senior Statistical Programmer (SDTM)

Redbock - an NES Fircroft company; Boston (MA); Remote; USD 83,000 - 165,000; Full time

Benefits offered by this job

Remote work

Contract position

Job summary

Redbock - an NES Fircroft company is seeking a Senior Statistical Programmer to join a growing biotech organization focused on advancing innovative therapies. This remote, contract role involves hands-on programming within a small, collaborative team, with opportunities to contribute across the full spectrum of SDTM data handling and regulatory submissions.

The ideal candidate will have extensive statistical programming experience in biotech/pharma/CRO settings, strong SDTM expertise, and the

Qualifications

• Significant experience in Statistical Programming within biotech/pharma/CRO industries.
• Strong expertise in SDTM and clinical data standards.
• Experience supporting clinical trials and regulatory submissions.
• Neuroscience experience strongly preferred.
• Demonstrated ability to work cross-functionally in small teams.

Responsibilities

• Lead and execute statistical programming activities supporting clinical development programs.
• Develop, validate, and maintain SDTM datasets and related study deliverables.
• Collaborate with Biostatistics, Data Management, Clinical Operations, and cross-functional teams.
• Support regulatory submission activities and ensure programming deliverables meet quality and compliance standards.
• Partner with stakeholders to troubleshoot issues and drive programming solutions.
• Contribute as an individual performer while supporting lean, dynamic team objectives.

Skills

Statistical programming

SDTM expertise

Regulatory submissions

Cross-functional collaboration

Neuroscience experience

Job description

Senior Statistical Programmer (SDTM) Remote | Contract Opportunity | Biotechnology/Neuroscience

We are seeking a Senior Statistical Programmer to join a growing biotech organization focused on advancing innovative therapies. This is a highly hands-on role within a small, collaborative team, making it an excellent opportunity for an experienced programmer who thrives in a fast-paced environment and can work independently with minimal oversight.

Key Responsibilities

• Lead and execute statistical programming activities supporting clinical development programs.
• Develop, validate, and maintain SDTM datasets and related clinical study deliverables.
• Collaborate closely with Biostatistics, Data Management, Clinical Operations, and other cross-functional teams.
• Support regulatory submission activities and ensure programming deliverables meet quality and compliance standards.
• Partner with technical and functional stakeholders to troubleshoot issues and drive programming solutions.
• Contribute as an individual performer while helping support the broader objectives of a lean and dynamic team.

Qualifications

• Significant experience in Statistical Programming within the biotech, pharmaceutical, or CRO industry.
• Strong expertise in SDTM and clinical data standards.
• Experience supporting clinical trials and regulatory submission activities.
• Neuroscience therapeutic area experience is strongly preferred.
• Demonstrated ability to work cross-functionally in smaller organizations or lean teams.
• Self-starter who can quickly assess priorities, take ownership, and deliver results with limited direction.
• Confident communicator with a proactive, problem-solving mindset.
• Experience working in highly technical and hands-on environments.

Ideal Candidate

We're looking for someone who is dedicated, hardworking, and comfortable wearing multiple hats. The successful candidate will be proactive, capable of hitting the ground running, and energized by working in a small team where collaboration and accountability are essential. Candidates located in or near the Eastern Time Zone are preferred.

If you're an experienced statistical programmer looking to make a meaningful impact within a growing biotech organization, we'd love to hear from you.