Biostatistician (Evening Shift)

Minerva is seeking a skilled Biostatistician to join its clinical research team in Karachi on a full-time, on-site basis. The successful candidate will play a vital role in supporting clinical research projects through rigorous statistical analysis, data interpretation, and comprehensive research reporting. This position demands a strong foundation in statistics and clinical research, with the ability to handle clinical data effectively and collaborate across various departments.

Key Responsibilities

- Analyze clinical research and study data using appropriate statistical methodologies.
- Provide statistical input during the planning and design phases of clinical studies.
- Perform sample size and power calculations as needed.
- Prepare and contribute to the development of Statistical Analysis Plans (SAPs).
- Conduct detailed statistical analyses and interpret study outcomes.
- Generate statistical tables, graphs, and reports to support findings.
- Review datasets to identify errors, trends, inconsistencies, and anomalies.
- Collaborate closely with Clinical Operations, Data Management, Regulatory, Quality Assurance, and other relevant teams.
- Communicate statistical results clearly to both clinical and non-statistical stakeholders.
- Assist in the preparation of Clinical Study Reports (CSRs) and scientific publications.
- Ensure all statistical activities comply with approved protocols, Standard Operating Procedures (SOPs), and applicable clinical research standards.
- Maintain accurate documentation and records of all statistical analyses performed.
- Support data reviews, quality checks, audits, and regulatory submissions as required.

Required Qualifications

- Bachelor’s or Master’s degree in Biostatistics, Statistics, Mathematics, Epidemiology, or a related discipline.
- Minimum of 3 years of relevant professional experience in biostatistics, clinical research, healthcare, pharmaceutical, or Contract Research Organization (CRO) settings.
- Strong knowledge of statistical methods and data analysis techniques.
- Good understanding of clinical trials and clinical research processes.
- Proficiency with statistical software such as R, SAS, SPSS, Python, or Stata.
- Advanced skills in Excel and data management.
- Excellent analytical and problem-solving capabilities.
- High attention to detail and accuracy in work.
- Effective written and verbal communication skills.

Preferred Qualifications and Benefits

Previous experience working within a CRO, pharmaceutical company, or clinical research organization is highly desirable. Familiarity with preparing or reviewing Statistical Analysis Plans (SAPs) and working with clinical trial datasets will be advantageous. Knowledge of ICH-GCP guidelines and clinical research standards is preferred. Experience with CDISC standards such as SDTM or ADaM is a plus. Proficiency in SAS or R software is especially valued.

Minerva offers the opportunity to work in a dynamic and growing clinical research organization. The role provides exposure to multidisciplinary clinical research projects and collaboration with experienced teams across Clinical Operations, Data Management, Regulatory Affairs, Quality Assurance, and Compliance. This position supports professional development and growth within the clinical research industry.