Manager, Statistical Programming

Scorpion Therapeutics; California (MO); On-site; USD 140,000 - 190,000; Full time

Job summary

Scorpion Therapeutics is seeking a Manager of Statistical Programming to lead the generation of analysis datasets and outputs that support regulatory and scientific submissions. You will partner with clinical teams and vendors to ensure high-quality tables, figures, and listings and to drive timely, compliant deliverables.

The role requires extensive SAS and CDISC experience in regulated environments, a strong foundation in trial design and regulatory processes, and the ability to coordinate

Qualifications

• 7+ years in pharma/biotech statistics programming or equivalent.
• Extensive experience with SAS and CDISC standards in regulated environments.
• Strong knowledge of clinical trial design and regulatory submissions.
• Experience with oncology, hematology, virology, or inflammation is a plus.

Responsibilities

• Generating study report tables, figures, and listings.
• Ensuring documentation compliance with departmental procedures.
• Supporting strategic initiatives within the programming function.
• Interacting with cross-functional teams to meet project timelines.

Skills

Communication

Analytical thinking

Problem solving

Education

Bachelor's degree in Biostatistics, Computer Science, or related field

MS in Biostatistics, Statistics, or related field

PhD in Biostatistics or related field

Tools

SAS

CDISC standards

Job description

Role

Manager of Statistical Programming responsible for collaboration with clinical teams and vendors to produce high-quality analysis datasets and statistical outputs supporting regulatory and scientific submissions.

Responsibilities

• generating study report tables, figures, listings
• ensuring documentation compliance with departmental procedures
• supporting strategic initiatives
• interacting with cross-functional teams to meet project timelines

Qualifications

• BS in Biostatistics, Computer Science, or related field with 7+ years in pharma/biotech, or MS with 3+ years, or PhD with 2+ years
• extensive experience with statistical programming (SAS, CDISC standards) in regulated environments
• strong knowledge of clinical trial design, regulatory reporting (FDA, EMA, PMDA), and regulatory submission processes, especially in oncology, hematology, virology, or inflammation

Skills

• excellent communication, problem-solving, and analytical capabilities
• proven ability to manage complex, time-sensitive projects and implement strategic initiatives

HighValue

• experience with pivotal studies, regulatory submissions (NDA, BLA, MAA), and integrated analysis activities
• knowledge of GxP, ICH standards, and electronic data submissions

WorkSetup

not specified.