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Clinical Data Statistical Analyst Jobs – Life Sciences Apply on Biotecnika
If you’re looking to grow a career in clinical research, data analytics, and biostatistics, this opportunity stands out as a strong entry point. Clinical Data Statistical Analyst Jobs – Life Sciences Apply on Biotecnika offers a pathway for candidates skilled in statistics, programming, and clinical data handling to work directly on real-world healthcare studies and maternal health research. With hands-on exposure, structured learning, and publication-focused work environments, this role is ideal for fresh professionals ready to step into biostatistics and clinical analytics.
Job Title: Clinical Data Statistical Analyst
Location: On-site, AFMC Pune
Organization: Dōtō Health | CareMother
Salary: Up to ₹35,000 per month
Experience: 0 to 1 Year ( Should have expertise in Statistics)
About the Role
Dōtō Health | CareMother is seeking a Clinical Data Statistical Analyst to support data-driven insights across clinical studies and maternal health research initiatives. The role involves statistical analysis of clinical data, development of analysis plans, collaboration with clinical and technical teams, and contribution to study reports and publications.
Key Responsibilities
• Perform comprehensive statistical analyses on data collected from clinical trials and studies, including descriptive statistics, inferential testing, survival analysis, and regression modeling.
• Develop and validate Statistical Analysis Plans (SAPs) in accordance with study protocols and regulatory guidelines (FDA, ICH, GCP).
• Generate tables, listings, figures (TLFs), and ad-hoc reports using statistical software to effectively communicate results to clinicians, regulatory teams, and internal stakeholders.
• Collaborate with clinical data managers, biostatisticians, and programmers to ensure data quality from initial cleaning and imputation to final dataset preparation.
• Support interim analyses, sample size calculations, and power estimations to guide study design and decision-making.
• Contribute to clinical study reports (CSRs), publications, and presentations by interpreting statistical outputs and providing meaningful insights.
• Maintain thorough documentation of all analyses, including code, assumptions, and validation processes to ensure reproducibility and audit readiness.
• Stay up to date with evolving statistical methodologies and tools relevant to clinical research, including adaptive trial designs and machine learning applications in biostatistics.
Qualifications & Requirements
Education
• Master’s degree in Biostatistics, Statistics, Public Health, Lifesciences or a related quantitative field.
Experience
• 0–2 years of hands-on experience in statistical analysis for clinical trials or pharmaceutical/biotech environments.
• Proven experience working with data from diagnostic assays.
Technical Skills
• Proficiency in R, SAS, Python (pandas, statsmodels), and/or SPSS.
• Experience with EDC systems such as Medidata Rave or Oracle Clinical.
• Knowledge of CDISC standards (SDTM, ADaM).
• Strong understanding of statistical concepts including hypothesis testing, ANOVA, logistic regression, and mixed-effects models.
Soft Skills
• Excellent analytical and problem-solving skills with strong attention to detail and data integrity.
• Strong communication skills to explain statistical concepts to technical and non-technical teams.
• Ability to work independently and collaboratively in fast-paced, deadline-driven settings.
• Commitment to ethical standards and confidentiality while handling sensitive clinical data.
Preferred Qualifications
• SAS Programming or Biostatistics certification.
• Experience with regulatory submissions (e.g., IND, NDA) or communication with health authorities.
• Familiarity with integrating patient counseling data into diagnostic studies.
• Publication record in peer-reviewed clinical or biostatistics journals.
