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Expert Biostatistician

9-16 years
Not Disclosed
10 Dec. 27, 2024
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: Expert Biostatistician

Location: PAN India (Mumbai)

Job Function: Business Process Services

Role: Executive

Experience Range: 9 to 18 years


Job Description:

TCS is hiring for the Expert Biostatistician role!

Responsibilities:

  1. Develop protocol in alignment with development plans, offering statistical, scientific, and operational inputs for trial design, reporting, and statistical deliverables.
  2. Lead statistical/numerical/analytic research, providing solutions and advice on computational aspects.
  3. Guide trial statisticians to ensure consistency and compliance with company standards across all trial documents.
  4. Oversee the reporting and execution of statistical analysis for multiple studies, leading statistical deliverable meetings and exploratory analyses.
  5. Manage Biostatistics resources and deliverables for assigned trials, ensuring timely and quality results.
  6. Explain statistical methodology and analysis results, providing statistical expertise to support clinical trial activities.
  7. Collaborate with other functions to ensure smooth trial execution, translating complex statistical concepts into understandable language.
  8. Develop and comply with project/study standards and specifications, ensuring quality control of all deliverables.
  9. Mentor and provide support to junior statisticians and new hires.
  10. Contribute to scientific collaborations, publications, and professional presentations to promote innovative statistical methods.
  11. Assist with the preparation of Clinical Trial Reports (CTR) and electronic submissions.

Qualifications:

  • Educational Qualifications: Bachelor's in Statistics, Engineering (BTech), or Master's in Statistics, Engineering, or related fields.

Desired Skills:

  • Statistical expertise
  • Strong problem-solving and leadership abilities
  • Knowledge of clinical trials and regulatory guidelines