What you will be doing:

- Contribute to the design of case report forms with a focus on statistical aspects.
- Review study database structures, edit checks, and data management coding conventions to ensure data integrity.
- Prepare comprehensive statistical analysis plans, defining derived data and crafting statistical tables, figures, and data listings for clinical summary reports.
- Conduct statistical analyses to extract meaningful insights from research data.
- Interpret data and effectively communicate findings through result reporting.
- Collaborate on writing the statistical methods sections of integrated study reports.

Your Profile:

- A Masters degree or higher in statistics or related field
- Demonstrated experience of 2+ years in statistics, biostatistics, or a related field within the pharmaceutical industry is required.




- Robust kNwledge of study designs and statistical analysis conventions in one or more therapeutic areas.
- Exceptional verbal and written communication skills and proficient computer skills.
- Strong familiarity with clinical trials methodology, regulatory requirements, statistics, and proficiency in statistical software packages, including SAS.

Ability to translate clients needs into statistical practices and educate clients in the utilization of statistical methods, coupled with solid interpersonal and project management skills.

#LI-KT

Skills: biostatistics , Statistical Analyst, Pharmaceutics, Project Management

Experience: 3.00-8.00 Years

📌 Biostatistician I & II (Thiruvananthapuram)
🏢 ICON
📍 Thiruvananthapuram