Biostatistician (Evening Shift)

Minerva, based in Karachi, Pakistan, is seeking an experienced Biostatistician to join their Clinical Research and Biostatistics department on a full-time, on-site basis. The successful candidate will play a vital role in supporting clinical research projects through comprehensive statistical analysis, data interpretation, and research reporting. This position requires a strong foundation in statistics and clinical research, with the ability to handle clinical data effectively and collaborate across multiple teams.

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

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

Preferred Qualifications and Benefits
- Previous experience working in a CRO, pharmaceutical, or clinical research organization.
- Experience preparing or reviewing Statistical Analysis Plans (SAPs).
- Familiarity with clinical trial datasets.
- Knowledge of ICH-GCP guidelines and clinical research standards.
- Understanding of CDISC standards such as SDTM or ADaM is advantageous.
- Preference given to candidates with experience in SAS or R programming.

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