Senior Manager, Biostatistics

Scorpion Therapeutics; Parsippany-Troy Hills (NJ); On-site; USD 120,000 - 170,000; Full time

Job summary

Scorpion Therapeutics is seeking a Biostatistics lead to support clinical studies within our biopharma pipeline, focusing on trial design, analysis, and regulatory submissions.

The role involves overseeing statistical analyses, developing analysis plans, and providing statistical input in cross-functional discussions while leading technical activities for complex trials.

Qualifications

• PhD in biostatistics or related field with 4+ years industry experience (PhD)
• Expertise in biomedical data analysis using SAS
• Experience managing projects or small teams

Responsibilities

• Oversee statistical analysis and review data for NDA submissions
• Develop analysis plans and provide statistical input in cross-functional teams
• Lead technical activities for complex clinical trials and contribute to regulatory documentation

Skills

Project management

Statistical analysis

Leadership

Cross-functional collaboration

Education

PhD in biostatistics

MS in biostatistics or related field

BA/BS in related field

Tools

SAS

Job description

Role

Biostatistics lead supporting clinical studies within Gilead's biopharma pipeline, focusing on trial design, analysis, and regulatory submissions.

Responsibilities

Oversee statistical analysis, review data for NDA submissions, develop analysis plans, provide statistical input in cross-functional team discussions, and lead technical activities for complex clinical trials. May manage projects or teams, contribute to methodology improvements, and support regulatory documentation.

Requirements

PhD in biostatistics or related field with 4+ years (PhD) or 6+ years (MS) or 8+ years (BA/BS) relevant industry experience, expertise in biomedical data analysis using SAS, and experience managing projects or small teams.

Preferred

Proven leadership, advanced statistical knowledge, and experience with clinical trial data, safety analysis, and biomarker studies.

High-Value

Supporting clinical development, regulatory submissions, and data analysis for therapies addressing infectious diseases and oncology, with involvement in multiple study phases.

Collaboration

Internal cross-functional teams, external partners, and regulatory authorities.

Work setup

Not specified, but the role involves technical leadership and project oversight.