Biostatistician (Evening Shift)

Minerva, a leading clinical research organization based in Karachi, Pakistan, is seeking an experienced Biostatistician to join our team on a full-time, on-site basis. The successful candidate will play a crucial role in supporting clinical research projects by performing statistical analyses, interpreting data, and contributing to research reporting. This role requires a strong foundation in statistics and clinical research, with the ability to work effectively with clinical data and collaborate across various departments.

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 support the development of Statistical Analysis Plans (SAPs).
- Conduct statistical analyses and interpret study results accurately.
- Prepare statistical tables, graphs, and comprehensive reports.
- Review data to identify errors, trends, inconsistencies, and unusual results.
- Collaborate closely with Clinical Operations, Data Management, Regulatory, Quality Assurance, and other teams.
- Communicate statistical findings clearly to both clinical and non-statistical team members.
- Assist in 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.
- Support data reviews, quality checks, audits, and meet 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 Contract Research Organization (CRO) settings.
- 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 in work.
- Strong written and verbal communication skills.

Preferred Qualifications and Benefits

Previous experience working in a CRO, pharmaceutical company, or clinical research organization is highly desirable. Candidates with experience preparing or reviewing Statistical Analysis Plans (SAPs) and working with clinical trial datasets will have an advantage. Familiarity with ICH-GCP guidelines and clinical research standards is preferred. Knowledge of CDISC standards such as SDTM or ADaM, as well as proficiency in SAS or R, will be considered a plus.

Minerva offers the opportunity to work within a growing clinical research organization, gaining exposure to multidisciplinary clinical research projects. You will collaborate with experienced teams across Clinical Operations, Data Management, Regulatory, Quality Assurance, and Compliance. This position provides excellent potential for professional growth within the clinical research industry.

If you are a detail-oriented biostatistician passionate about clinical research and eager to contribute to impactful projects, Minerva welcomes your application.