Clinical Data Analyst Job | Remote Fortrea Jobs in Bangalore
A clinical data analyst job is a critical role in clinical research, supporting data quality, compliance, and the timely delivery of clinical trial results. This opportunity is ideal for professionals seeking remote jobs within global Fortrea jobs, offering exposure to early-phase studies while working full-time from Bangalore in a home-based environment.
Job Details:
- Job Title: Sr Clinical Data Analyst (Early Studies)
- Job type: Remote
- Locations: Bangalore
- Time type: Full-time
- Last Date: January 18, 2026
- Job requisition ID: 2671
About the Company
Fortrea is a global organization delivering clinical research and drug development solutions across early and late-phase studies. Among leading Fortrea jobs, the company supports high-quality clinical data management, regulatory compliance, and harmonized global SOPs while offering flexible remote jobs and strong career growth opportunities.
Qualifications
- University/college degree in health sciences or related subjects, or certification in allied health professions.
- Fluent in English, both written and verbal.
Experience Required
- 3 to 4 years of applicable experience in clinical research (Data Management preferred).
- Additional experience may be substituted for education requirements.
- Knowledge of medical terminology.
- Knowledge of the drug development process.
- Knowledge of effective clinical data management practices.
- Strong time management, organizational, communication, and collaboration skills.
Job Description
This clinical data analyst job is part of Fortrea jobs designed for professionals seeking long-term remote jobs while contributing to global clinical research programs.
Key Responsibilities
- Ensures that all allocated projects are carried out in strict accordance with relevant protocols, global harmonized SOPs, and GCP standards.
- Perform all data management tasks, including data review and query management, to meet quality standards within stipulated timelines.
- Assist with reviewing clinical trial data in accordance with Data Management Plans, Edit Check Specifications, and Data Review Guidelines.
- Generate, resolve, and track queries identified during aggregate data review activities.
- Run additional programs, special listings, and reconciliation discrepancy listings to support clinical trial data review.
- Interact with project team members to support the setup, maintenance, and closure of the project’s Data Management aspects.
- Assist with reviewing data listings for internal data review.
- Assist or create dummy data to test edit checks, database screen design, SAS reports, and data listings.
- Modify standard templates to create study-specific Data Management Plans and eCRF completion guidelines.
- Support documentation posting, data management, administrative tasks, and eTMF maintenance.
- Generate study status reports and perform database extracts.
- Assist in Investigator Meetings and Site Initiation Visit presentations.
- Assist with Database Lock activities.
- Support training of new staff on project-specific Data Management processes.
- Perform any other duties as assigned
