A Biostatistician in Clinical Research plays a critical role in the design, analysis, and interpretation of data in clinical trials and other research studies. Their main responsibility is to apply statistical methods to biomedical research data to draw meaningful conclusions and inform decision-making in the field of healthcare. A comprehensive job description for a biostatistician in clinical research

Key Responsibilities:

• Study Design: Collaborate with researchers, clinicians, and other stakeholders to design clinical trials and observational studies. Determine sample sizes, randomization methods, and statistical methodologies to ensure study objectives are met.
• Statistical Analysis: Perform data analysis using appropriate statistical techniques and software. Conduct exploratory data analysis, develop statistical models, and apply statistical inference methods to evaluate treatment effects, patient outcomes, and other relevant endpoints.
• Data Management: Oversee data collection, cleaning, and quality control procedures. Ensure accurate and reliable data entry, implement data validation checks, and resolve data discrepancies. Develop data management plans and standard operating procedures for data handling.
• Statistical Programming: Utilize statistical software (e.g., SP SAS, Python) to write and execute programs for data manipulation, analysis, and visualization. Develop and maintain analysis code, macros, and scripts for efficient data processing and statistical modeling.
• Statistical Reporting: Prepare statistical reports, summaries, and presentations for study investigators, regulatory agencies, and scientific publications. Communicate results effectively to both technical and non-technical audiences, providing clear interpretations and implications of the findings.
• Regulatory Compliance: Ensure compliance with relevant regulatory guidelines, such as Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. Participate in the development of study protocols, informed consent forms, and statistical analysis plans.
• Collaboration and Consultation: Collaborate with cross-functional teams including researchers, clinicians, data managers, and regulatory affairs personnel. Provide statistical expertise and guidance throughout the research process. Act as a consultant on statistical design and analysis for colleagues and stakeholders.
• Literature Review: Stay up to date with the latest statistical methodologies, clinical trial designs, and regulatory requirements. Conduct literature reviews and participate in professional development activities to enhance statistical knowledge and skills.
• Quality Assurance: Contribute to quality assurance activities to ensure data integrity, protocol adherence, and overall study quality. Perform quality control checks on statistical analyses and contribute to the development of quality improvement initiatives.
• Continuous Improvement: Identify opportunities to improve statistical methodologies, data analysis techniques, and research processes. Propose and implement innovative approaches to enhance efficiency, accuracy, and reproducibility in statistical analysis

Qualifications and Skills:

• A master's or doctoral degree in biostatistics, statistics, or a related field with 3 to 5 years of experience as biostatistician in clinical research organization (CRO), pharmaceutical, healthcare industries, Research Institution, and health department.
• Proficiency in statistical software such as SP SAS, or Python.
• Strong knowledge of statistical methodologies, including regression analysis, survival analysis, longitudinal data analysis, and clinical trial designs.
• Familiarity with regulatory guidelines and standards in clinical research.
• Excellent data management and programming skills.
• Strong analytical and problem-solving abilities.
• Effective communication skills, both written and verbal, to convey complex statistical concepts to diverse audiences.
• Attention to detail and ability to work with large and complex datasets.
• Ability to work independently and collaboratively in a team-oriented environment.

Patanjali Research Foundation is an equal opportunity employer and does not discriminate against any applicant because of race, colour, religion, gender, national origin, age and physical disability.

How to Apply

• Write to jobs@patanjali.res.in with your detailed CV and career aspirations.
• Mention Biostatistician, citing respective Job Code.
• List three professional references other than your friends and family.