Evening Biostatistician — Clinical Trials Analyst

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

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.