Global Clinical Submissions Lead — SAS Programming

Scorpion Therapeutics; New Jersey; On-site; USD 151,000 - 246,000; Full time

Job summary

Scorpion Therapeutics seeks an experienced lead SAS programmer to drive programming in clinical data for multiple studies. You will guide standards, collaborate across global teams, and deliver submission-ready programming for regulatory filings.

The role requires strong mentoring skills, hands-on programming, and the ability to influence project direction while maintaining high-quality outputs. A strategic mindset and cross-functional partnership are essential.

Qualifications

• Advanced SAS programming in a clinical data environment.
• Strong understanding of clinical trial principles and regulatory submission requirements.
• Experience leading global, cross-functional teams.
• Mentoring/coaching experience with junior programmers.
• Excellent collaboration and communication across study teams.

Responsibilities

• Lead programming support across multiple studies, ensuring timely, high-quality deliverables.
• Coordinate programming documentation and specifications, following established standards.
• Communicate proactively with study and project teams to clarify requirements and guide programmers.
• Lead submission-ready programming deliverables for global regulatory authority filings.
• Guide the development of direct reports through goal-setting, coaching, and mentoring.
• Contribute to hiring by screening and interviewing programming candidates.

Job description

Scorpion Therapeutics seeks an experienced lead SAS programmer to drive programming in clinical data for multiple studies. You will guide standards, collaborate across global teams, and deliver submission-ready programming for regulatory filings.

The role requires strong mentoring skills, hands-on programming, and the ability to influence project direction while maintaining high-quality outputs. A strategic mindset and cross-functional partnership are essential.