Senior Biostatistician: Pharma experience / Remote

Senior Biostatistician: Pharma experience / Remote

Posted 1 week ago by 1753349081

Negotiable
Outside
Remote
USA

Summary: Biogensys is seeking a Senior Biostatistician with extensive Pharma experience for a remote contract position lasting between 6 to 12 months. The role requires a seasoned professional to lead statistical aspects of clinical studies and mentor junior staff. Candidates must have a strong background in SAS and/or R, along with a commitment to compliance with industry standards. Sponsorship is not available for this position.

Key Responsibilities:

  • Lead statistical aspects of clinical studies from design to final reporting
  • Review and approve programming deliverables (ADaM datasets, tables, listings, and figures)
  • Proven expertise in SAS and/or R for statistical analysis
  • Mentor junior biostatisticians and support team development
  • Ensure compliance with industry standards (CDISC, ICH, FDA/EMA guidelines)
  • Draft SAP/shell independently
  • Work in detail and able to review the TLF
  • Excellent communication and leadership skills with cross-functional collaboration experience

Key Skills:

  • At least 9-10 years of experience
  • Bachelor's or master's in computer science or related field

Salary (Rate): undetermined

City: undetermined

Country: USA

Working Arrangements: remote

IR35 Status: outside IR35

Seniority Level: Senior

Industry: Other

Detailed Description From Employer:

Biogensys is currently hiring Senior Biostatistician with Pharma experience for 6 to 12 months contract on w2. This is a remote position, no corp to corp, or 1099. No sponsorship is available.

Senior Biostatistician: Pharma experience / Remote-

  • At least 9-10 years of experience
  • Lead statistical aspects of clinical studies from design to final reporting
  • Review and approve programming deliverables (ADaM datasets, tables, listings, and figures)
  • Proven expertise in SAS and/or R for statistical analysis
  • Mentor junior biostatisticians and support team development
  • Ensure compliance with industry standards (CDISC, ICH, FDA/EMA guidelines)
  • Draft SAP/shell independently.
  • Work in detail and able to review the TLF;
  • Excellent communication and leadership skills with cross-functional collaboration experience

Education:

  • Bachelor s or master s in computer science or Related Field