Mendine Pharmaceuticals Pvt. Ltd. has announced an exciting opportunity for aspiring biostatistics professionals by opening applications for a Biostatistics Intern position in Kolkata. This six-month internship offers hands-on exposure to clinical trial data analysis, statistical programming, regulatory documentation, and collaboration with clinical research teams.
Candidates with backgrounds in Biostatistics, Statistics, Mathematics, or related disciplines and an interest in pharmaceutical research and clinical data analytics are encouraged to apply.
Job Overview
- Position: Biostatistics Intern
- Company: Mendine Pharmaceuticals Pvt. Ltd.
- Location: Kolkata, West Bengal, India
- Internship Duration: 6 Months
- Stipend: ₹10,000 per month
- Start Date: July 20, 2026
- Application Deadline: July 15, 2026
- Openings: 1
Key Responsibilities
Study Design and Planning
- Collaborate with clinical research teams to define study objectives and endpoints.
- Assist in protocol development and sample size determination.
- Support statistical methodology selection for clinical studies.
Statistical Analysis and Reporting
- Perform statistical analyses using SAS and R programming.
- Prepare datasets and generate Tables, Listings, and Figures (TLFs).
- Assist in preparing Clinical Study Reports (CSRs).
Regulatory Compliance
- Ensure analyses comply with ICH-GCP guidelines and regulatory standards.
- Support documentation for WHO, CDSCO, and FDA submissions.
- Contribute to Statistical Analysis Plans (SAPs).
Data Integrity and Collaboration
- Coordinate with data management teams on Case Report Forms (CRFs).
- Review datasets for consistency and accuracy.
- Maintain documentation and statistical records.
Eligibility Criteria
Educational Qualifications
- Bachelor’s degree in Statistics or Mathematics preferred.
- Master’s degree (M.Sc./M.Stat.) in Statistics, Biostatistics, Mathematics, or related disciplines preferred.
- PhD candidates in Biostatistics or Statistics may also apply.
Preferred Skills
- Knowledge of Biostatistics and Clinical Trial Methodology
- Proficiency in SAS Programming
- Experience with R Programming and Statistical Modeling
- Understanding of ANOVA and Predictive Modeling
- Knowledge of Clinical Trial Phases I-IV
- Familiarity with ICH-GCP, WHO, CDSCO, and FDA guidelines
- Exposure to SPSS and Clinical SAS Programming is an added advantage
- Strong analytical and communication skills
Internship Benefits
Selected candidates will receive:
- Monthly stipend of ₹10,000
- Internship completion certificate
- Flexible working hours
- Letter of recommendation
- Potential job offer based on performance
- College credits, wherever applicable
- Hands-on experience in pharmaceutical and clinical research data analysis
Why This Internship Matters
The demand for professionals skilled in Biostatistics, SAS Programming, Clinical Data Analysis, and Regulatory Statistics continues to grow across pharmaceutical companies and Contract Research Organizations (CROs). This internship provides practical exposure to real-world clinical trial data and regulatory standards, making it an excellent opportunity for students and early-career professionals looking to build a career in clinical research and biostatistics.
How to Apply
