hirly

VITELY CORP PVT LTD

Biostatistician Lead

Ahmedabad

See how you match this job — and similar ones. Free.

Upload your resume and hirly scores it against this role at VITELY CORP PVT LTD first, then against similar open jobs, and shows where you fit and why.

PDF or DOCX, up to 12MB. No sign-up to see your matches.

Get past the screening software and onto a recruiter's desk

hirly rewrites your resume for this job — matching the keywords and skills in the posting, moving your most relevant experience to the top, and writing a cover letter to fit. About 30 seconds.

  • Keywords matched to this posting
  • Fit score before you apply
  • Cover letter included

Matched against 2.3M live jobs from 200,000+ employers in 200+ countries.

Tailor my resume for this job →

hirly's read of this role

Seniority
Lead / management
Country
IN
Work mode
On-site / unstated
First seen by hirly
23 Sept 2026

Derived automatically from the posting. Upload your resume above to see how the role scores against it.

the posting

Job Summary

We are seeking a skilled In Vitro Statistician with 4+ years of experience to support our research and development teams in statistical analysis of in vitro studies. The ideal candidate will be responsible for designing experiments, analyzing data, and providing statistical insights to support decision-making in pharmaceutical, biotechnology, or life sciences research.

Key Responsibilities:

  • Design, develop, and analyze in vitro study experiments, ensuring statistical rigor and accuracy.
  • Apply appropriate statistical models and methodologies for data interpretation.
  • Work closely with scientists, biologists, and researchers to provide statistical guidance in study design and result evaluation.
  • Utilize statistical software (e.g., SAS, R, JMP, or Python) to conduct data analysis, visualization, and reporting.
  • Validate and verify data integrity, ensuring compliance with regulatory guidelines (FDA, ICH, GLP).
  • Develop and review statistical analysis plans (SAPs), study protocols, and technical reports.
  • Support regulatory submissions by preparing statistical documentation and reports.
  • Stay updated with the latest statistical methods and best practices in in vitro research.

Required Qualifications & Skills:

  • Master’s or Ph.D. in Statistics, Biostatistics, Bioinformatics, or a related field.
  • 2-7 years of experience in statistical analysis of in vitro studies, preferably in the pharmaceutical, biotechnology, or life sciences sector.
  • Strong knowledge of experimental design, regression models, ANOVA, DOE, and multivariate analysis.
  • Proficiency in statistical software (SAS, R, JMP, Python, or equivalent).
  • Experience with data visualization, trend analysis, and predictive modeling.
  • Understanding of regulatory requirements and compliance standards (FDA, ICH, GLP).
  • Excellent communication skills to present findings to cross-functional teams.
  • Strong problem-solving skills and attention to detail.

Preferred Qualifications:

  • Experience in bioassays, pharmacokinetics, biomarker analysis, or toxicology studies.
  • Familiarity with machine learning and AI-based statistical modeling.
  • Knowledge of clinical and preclinical statistical applications.
Original posting on VITELY CORP PVT LTD's site ↗

Want this one?

Upload your resume and hirly rewrites it for this job and writes the cover letter — in about thirty seconds, before you sign up.

Tailor my resume for this job