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Principal Biostatistician Fsp

9+ years
Not Disclosed
10 Feb. 17, 2025
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences 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

Job Title: Principal Biostatistician FSP
Location: Remote, Pune, Maharashtra, India
Job Type: Full-time
Posted: Dec. 17, 2024
Job ID: 286

Job Overview:

As a Principal Biostatistician, you will lead Phase I-IV clinical studies across the region and be dedicated to one of Cytel's global pharmaceutical clients. This is an exciting opportunity to work on innovative clinical development programs while collaborating closely with cross-functional teams. You will play a pivotal role in providing statistical expertise and leading analysis using advanced statistical methods, including machine learning algorithms, to enhance clinical development processes and patient treatment.

Responsibilities:

  • Work with the senior data science team to design and analyze A/B and multivariate hypothesis tests aimed at optimizing clinical outcomes.

  • Develop automation processes to streamline the analysis and insights generation.

  • Collaborate with global teams to solve critical business problems and deliver strategic initiatives.

  • Manage your own tasks and lead project management efforts to meet deadlines, anticipate changes, and align with stakeholders' expectations.

  • Utilize statistical methods, machine learning, and deep learning to mine data sources and create actionable insights.

  • Independently apply research methodologies to solve clinical development challenges.

Qualifications:

  • Education: Master's degree in Statistics or a related field (PhD is strongly preferred).

  • Experience: 9+ years in clinical trials within the pharmaceutical or biotechnology industry.

  • Skills:

    • Strong SAS programming skills for quality control, efficacy/safety tables, and working with programmers.

    • Knowledge of R programming (R Shiny, Python).

    • Ability to work independently, lead teams, and demonstrate initiative and flexibility.

    • Strong attention to detail, excellent interpersonal and communication skills, and innovative problem-solving abilities.

About Cytel:

Cytel is a leader in the clinical trial design and analytics space, offering statistical software and advanced analytics solutions. As a Principal Biostatistician at Cytel, you will contribute to the success of clinical trials and work alongside industry leaders in a dynamic and collaborative environment.