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Biostatistician

10+ years
Not Disclosed
10 Jan. 31, 2025
Job Description
Job Type: Full Time Education: MSc/PhD Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

📌 Biostatistician | Service Delivery - Warsaw, Poland (Remote)
📍 Location: Remote, Poland
💼 Company: Sitero
🕒 Experience: 10+ years in Biostatistics

Role Overview

The Biostatistician will provide advanced statistical support for clinical studies, including study design, statistical analysis, and regulatory engagement. This position requires expertise in CDISC standards, SAS programming, and experience supporting regulatory submissions. The Biostatistician will also collaborate with clients and contribute to sales efforts by offering statistical solutions.

Key Responsibilities

Statistical Expertise: Strong understanding of statistical principles and robust skills to provide support throughout clinical studies.
Statistical Analysis: Conduct analyses of clinical data, interpreting results for drug efficiency and safety, and study goals.
Study Design & Reporting: Calculate sample sizes, develop concepts and protocols, create SAPs, and prepare clinical study reports for regulatory submissions.
Regulatory Engagement: Engage with FDA and EMEA regulators, preparing statistical documentation and communicating plans and results.
DMC/DSMB Support: Provide support for Data Monitoring Committees (DMC), including charter development, SAP, and mock tables, listings, and figures (TLFs) for DSMB support.
CDISC Compliance: Ensure adherence to CDISC standards, especially SDTM and ADaM specifications, for regulatory submissions.
SAS Proficiency: Extensive experience in SAS for statistical analysis, creating and validating TLFs for NDA and BLA submissions.
Client Interaction & Sales Support: Engage with clients to understand their statistical needs, providing expert advice and solutions.
SOP Development: Create and update Standard Operating Procedures (SOPs) for statistical processes and regulatory submissions.

Qualifications

🎓 Education:

  • MSc or PhD in Biostatistics or Statistics.

💼 Experience:

  • 10+ years of experience as a Biostatistician in CRO/Pharma/Biotech.
  • 3+ years of experience leading a team of biostatisticians and statistical programmers.

Desired Skills

  • Proficiency in SAS, R, or Python.
  • Experience with BASE, STAT, MACRO, GRAPH, and TLFs.
  • Strong knowledge of regulatory guidelines and statistical methodologies for clinical development.
  • Excellent written and verbal communication skills.
  • Ability to mentor new team members and support their onboarding.
  • Strong knowledge of ICH guidelines.

Benefits

  • Competitive salary and variable pay.
  • Healthcare and retirement benefits.
  • Paid time off.

Work Environment

  • Full-Time, Permanent position, remote work option.

📩 Apply Now