Biostatistician (Evening Shift)

Minerva Research Solutions; Karachi Division; On-site; PKR 1,800,000 - 2,400,000; Full time

Job summary

Minerva Research Solutions in Karachi, Pakistan seeks an experienced Biostatistician to support clinical research projects through statistical analysis, data interpretation and reporting. You will collaborate with cross-functional teams and ensure adherence to ICH-GCP standards.

The role covers SAP preparation, study design input, sample size calculations, and preparation of CSR manuscripts, with on-site work and a focus on accuracy and clear communication.

Qualifications

• Minimum 3 years of relevant professional experience in biostatistics or clinical research.
• Strong understanding of statistical methods and data analysis.
• Hands-on experience with statistical software (R, SAS, SPSS, Python or Stata).
• Good written and verbal communication skills.
• Knowledge of clinical trials processes.

Responsibilities

• Analyze clinical research data using appropriate statistical methods.
• Provide statistical support during planning and design of studies.
• Perform sample size and power calculations as needed.
• Prepare and support SAPs and CSRs.
• Communicate statistical findings to non-statistical teams.
• Review data for errors, trends, inconsistencies.
• Maintain records and documentation of analyses.
• Collaborate with Clinical Operations, Data Management, Regulatory, QA, and Compliance teams.

Skills

Biostatistics

Clinical Research

Statistical Analysis

Data Analysis

Clinical Trials

Statistical Reporting

R/SAS

Excel

Data Interpretation

SAP

ICH-GCP

Education

Bachelor's or Master's degree in Biostatistics, Statistics, Mathematics, Epidemiology, or a related field

Tools

SAS

R

SPSS

Python

Stata

Job description

Company: Minerva
Location: Karachi, Pakistan
Employment Type: Full-Time
Department: Clinical Research / Biostatistics
Work Mode: On-Site

About The Role

Minerva is looking for an experienced Biostatistician to support our clinical research projects through statistical analysis, data interpretation, and research reporting. The ideal candidate should have strong knowledge of statistics and clinical research, with the ability to work with clinical data and collaborate with different teams.

Key Responsibilities

• Analyze clinical research and study data using appropriate statistical methods
• Provide statistical support during the planning and design of clinical studies
• Perform sample size and power calculations when required
• Prepare and support Statistical Analysis Plans (SAPs)
• Conduct statistical analysis and interpret study results
• Prepare statistical tables, graphs, and reports
• Review data to identify errors, trends, inconsistencies, and unusual results
• Work closely with Clinical Operations, Data Management, Regulatory, QA, and other teams
• Clearly communicate statistical findings to clinical and non-statistical team members
• Support preparation of Clinical Study Reports (CSRs) and research publications
• Ensure statistical activities follow approved protocols, SOPs, and applicable clinical research standards
• Maintain accurate records and documentation of statistical analyses
• Support data reviews, quality checks, audits, and regulatory requirements when needed

Requirements

• Bachelor's or Master's degree in Biostatistics, Statistics, Mathematics, Epidemiology, or a related field
• Minimum 3 years of relevant professional experience in biostatistics, clinical research, healthcare, pharmaceutical, or CRO environments
• Strong understanding of statistical methods and data analysis
• Good understanding of clinical trials and clinical research processes
• Hands-on experience with statistical software such as R, SAS, SPSS, Python, or Stata
• Strong Excel and data-handling skills
• Strong analytical and problem-solving abilities
• Excellent attention to detail and accuracy
• Good written and verbal communication skills

Preferred Qualifications

• Previous experience in a CRO, pharmaceutical, or clinical research organization
• Experience preparing or reviewing Statistical Analysis Plans (SAPs)
• Experience working with clinical trial datasets
• Knowledge of ICH-GCP and clinical research guidelines
• Familiarity with CDISC, SDTM, or ADaM is an advantage
• Experience with SAS or R will be preferred

Key Skills

Biostatistics | Clinical Research | Statistical Analysis | Data Analysis | Clinical Trials | Statistical Reporting | R/SAS | Excel | Data Interpretation | SAP | ICH-GCP

What We Offer

• Opportunity to work in a growing clinical research organization
• Exposure to multidisciplinary clinical research projects
• Collaboration with experienced Clinical Operations, Data Management, Regulatory, QA, and Compliance teams
• Professional growth within the clinical research industry