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Assistant Manager/Deputy Manager - Biostatistician

Hetero
Hetero
5-8 years
Not Disclosed
10 Jan. 15, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

ssistant Manager / Deputy Manager – Biostatistician

Location: Sanathnagar, Hyderabad, Telangana, India
Employment Type: Permanent
Experience Required: 5–8 Years
Functional Area: Biostatistics / Clinical Data Analysis


Job Overview

We are seeking an experienced Assistant Manager / Deputy Manager – Biostatistician to provide advanced statistical expertise in clinical research and data analysis. The role involves designing clinical studies, developing statistical analysis plans, performing complex data analyses, and ensuring compliance with regulatory and industry standards.

The ideal candidate will collaborate with cross-functional teams, including clinical researchers, medical experts, and data scientists, to ensure robust statistical methodologies are applied across clinical trials, epidemiological studies, and observational research.


Key Responsibilities

1. Study Design & Statistical Planning

  • Collaborate with clinical and medical teams to design clinical studies and research protocols.

  • Develop Statistical Analysis Plans (SAPs), defining primary/secondary endpoints, sample size calculations, and statistical methodologies.

  • Advise on randomization techniques, adaptive designs, and emerging statistical approaches.

  • Ensure statistical methods comply with regulatory requirements and industry standards, including GCP and GSP.

2. Data Analysis & Interpretation

  • Lead analysis of complex datasets from clinical trials, observational, and epidemiological studies.

  • Perform data cleaning, transformation, and validation to ensure integrity.

  • Apply advanced statistical software (R, SAS, STATA) and techniques, including regression models, survival analysis, and mixed models.

  • Analyze results, ensuring scientifically sound conclusions, and communicate findings clearly to technical and non-technical stakeholders.

3. Advanced Methodologies & Quality Control

  • Develop and apply advanced statistical methodologies (e.g., longitudinal analysis, Bayesian methods) tailored to study requirements.

  • Assess and adapt statistical methods based on emerging data or evolving study designs.

  • Conduct quality control on statistical analyses to ensure accuracy and validity.

4. Reporting & Communication

  • Prepare statistical reports, manuscripts, presentations, and posters for scientific journals, conferences, and internal stakeholders.

  • Present complex statistical results to non-statistical audiences, ensuring clarity and actionable insights.

5. Collaboration & Strategic Input

  • Work closely with clinical researchers, project managers, and data scientists to align analyses with research objectives.

  • Participate in regulatory meetings and scientific strategy sessions, providing statistical justification and insights to guide study design.

  • Translate statistical findings into actionable recommendations for decision-making.

6. Mentoring & Training

  • Mentor junior biostatisticians and team members on statistical methodologies, software, and best practices.

  • Develop and conduct training workshops on statistical topics for internal teams and collaborators.

7. Compliance & Ethics

  • Ensure all statistical analyses adhere to ethical standards, patient safety, and data confidentiality.

  • Support the development of ethical guidelines for statistical methodologies in clinical research.


Required Qualifications and Experience

  • Education: M.Sc. / M.Stat / M.Tech in Biostatistics, Statistics, Mathematics, or related field.

  • Experience: 5–8 years in clinical biostatistics, clinical trial data analysis, or research analytics.

  • Hands-on experience with R, SAS, STATA, or similar statistical software.

  • Strong knowledge of regulatory standards, GCP, GSP, and clinical trial methodologies.

  • Proven ability to analyze complex datasets, develop SAPs, and communicate statistical insights effectively.


Key Skills & Competencies

  • Clinical Study Design & Statistical Planning

  • Advanced Data Analysis & Modeling

  • Statistical Software (R, SAS, STATA)

  • SAP Development & Regulatory Compliance

  • Signal Detection & Data Interpretation

  • Quality Control & Method Validation

  • Scientific Reporting & Presentation

  • Mentoring & Cross-Functional Collaboration


Why Join

  • Lead advanced biostatistical analyses in a growing clinical research environment.

  • Work with cross-functional global teams on clinical trials and research studies.

  • Opportunity to apply innovative statistical methodologies and contribute to high-impact publications.

  • Develop as a key biostatistics professional with exposure to regulatory and industry best practices.


Explore more global biostatistics, clinical research, and data analytics roles at
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