Senior Biostatistician - India

Planet Pharma

Thiruvananthapuram

On-site

INR 3,000,000 - 4,200,000

Full time

11 days ago
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Job summary

Planet Pharma is seeking a Senior Biostatistician in India to drive statistical excellence in clinical trials. You will collaborate with cross-functional teams to shape analyses, review SAPs, and ensure adherence to regulatory standards across multiple trial phases.

The role requires strong SAS and R skills, experience with SDTM/ADAM, and excellent communication to liaise with clients and teams. Remote work is welcomed, with preference for India-based candidates.

Qualifications

  • 5+ years of hands-on biostatistics experience in pharma/biotech.
  • Proven track record in statistical reviews and analysis across Phase 1–4.
  • Proficient in SAS and R, including ADAM/SDTM/CRF specs.
  • Skilled in ANCOVA, MMRM, chi-square, Fisher exact, logistic reg, KM curves.
  • Experience authoring SAP and mock TLF shells; review deliverables.

Skills

5+ years experience
Biostatistics
SAS
R programming
Statistical methods (ANCOVA, MMRM, etc
SAP & SAP review
Randomization & sample size
Communication skills
TMF filing & publications

Education

Bachelor’s or Master’s in Biostatistics/Statistics

Tools

SAS
R

Job description

Senior Biostatistician – India

Join a dynamic team at the forefront of clinical research and biostatistics, where your expertise will drive impactful health solutions across global markets. This strategic hire offers a unique opportunity to collaborate with our client, a Global CRO. You will play a pivotal role in advancing innovative clinical trials. If you’re passionate about statistical excellence, cross-functional collaboration, and making a difference in healthcare, this is your chance to shine.

What You’ll Need
  • Over 5 years of hands-on experience in biostatistics within the pharmaceutical or biotech industry
  • Proven track record in statistical reviews, methodological development, and analysis across clinical phases 1-4
  • Strong proficiency in SAS and R programming, including ADAMS, datasets, CRF, SDTM, and ADAM specifications
  • Expertise in statistical methods such as ANCOVA, MMRM, Chi-square, Fisher exact, Logistic regression, Kaplan-Meier, and Log Rank
  • Experience authoring Statistical Analysis Plans (SAP), mock TLF shells, and reviewing deliverables
  • Knowledge of randomization, sample size calculation, and validation
  • Excellent communication skills with the ability to liaise effectively with cross-functional teams and clients
  • Familiarity with TMF filing and scientific publication review
Nice To Have Skills
  • Co-lead experience and client negotiation skills
  • Knowledge of complex statistical methods including Bayesian approaches, missing data/sensitivity analyses with Multiple Imputation, and Negative Binomial regression
  • Experience in co-study leadership and exposure to complex efficacy analyses
Preferred Education & Experience
  • Bachelor’s or Master’s degree in Biostatistics, Statistics, or a related field
  • 5+ years of industry experience with a focus on clinical trial data analysis
  • Prior experience working remotely is welcomed; flexibility in work location preferred

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