Fortrea is inviting applications for the Biostatistician I position in Bangalore. The role involves statistical analysis for clinical studies, preparation of Statistical Analysis Plans (SAPs), Table, Figure, and Listing (TFL) reviews, and generation of randomization schedules.
Candidates with a bachelor’s degree, knowledge of statistical programming, and 0–2+ years of clinical trial experience can apply.
Fortrea Biostatistician I Recruitment – Job Details
| Job Detail | Information |
|---|---|
| Company | Fortrea |
| Job Title | Biostatistician I |
| Job Location | Bangalore |
| Employment Type | Full-time |
| Experience | 0–2+ years of clinical trial experience |
| Qualification | Bachelor’s degree |
| Preferred Qualification | Master’s degree or higher in Biostatistics or a related field |
| Job Requisition ID | 266121 |
| Application Deadline | October 20, 2026 |
Position
Fortrea is recruiting for the Biostatistician I position, which includes responsibilities related to clinical pharmacology studies and statistical support for clinical trials.
Roles and Responsibilities
Selected candidates will be responsible for:
- Performing the Lead Biostatistician role for clinical pharmacology studies.
- Monitoring project budgets and tasks for assigned studies.
- Assisting in the preparation of Statistical Analysis Plans, including mock TFL shells, under senior statistical staff supervision.
- Performing statistical analyses for simple and medium-complexity studies under senior staff direction.
- Conducting TFL reviews under supervision.
- Generating randomization schedules based on provided specifications.
- Performing other duties as assigned.
Eligibility and Qualifications
Candidates applying for the Fortrea Biostatistician I job must meet the following requirements:
- Educational Qualification: Bachelor’s degree.
- Experience: Minimum of 0–2+ years of clinical trial experience, or an equivalent combination of education and experience.
- Preferred Qualification: Master’s degree, equivalent, or higher in Biostatistics or a related field.
- Relevant and equivalent experience may be considered in place of educational requirements.
Required Skills
- Statistical programming using one or more statistical software packages, with SAS preferred.
- Ability to perform statistical analyses.
- Understanding of clinical trial statistics.
- Ability to prepare Statistical Analysis Plans and mock TFL shells.
- Knowledge of TFL review and randomization schedule generation.
- Effective communication of statistical concepts.
- Ability to work under the direction of senior statistical staff.
Work Environment and Travel
- Work setting: Office or home-based, as requested by the line manager.
- Travel requirement: 2–3% of working time.
- Overnight travel: Up to 50% of the travel time.
- Travel purpose: Client meetings and training.
