Fortrea, a leading global contract research organization (CRO), has announced exciting career opportunities for experienced professionals in Clinical Data Management and Clinical Operations. The company is currently hiring for Programmer and Clinical Research Associate (CRA) positions in Bangalore, India.
If you have experience in SAS Programming, Medidata Rave, Oracle InForm, Clinical Data Management, EDC Systems, Clinical Monitoring, or ICH-GCP, these Fortrea jobs offer an excellent opportunity to grow your career with one of the world’s leading clinical research organizations.
1. Programmer โ Clinical Data Management
Company: Fortrea
Job Location: Bangalore, India
Employment Type: Full-Time
Experience Required: 3โ5 Years
Application Deadline: August 7, 2026
Key Responsibilities
- Develop and maintain SAS programs for clinical datasets.
- Design and support databases using Medidata Rave and Oracle InForm.
- Create CRF annotations and mapping specifications.
- Perform EDC programming and edit check development.
- Generate reports, listings, and data visualizations.
- Import and reconcile external clinical data.
- Ensure compliance with CDISC standards.
- Support clinical database maintenance throughout studies.
- Work according to GCP, SOPs, and regulatory guidelines.
- Collaborate with Data Management and Biostatistics teams.
Required Qualifications
Applicants should possess one of the following:
- B.Pharm
- M.Pharm
- Pharm.D
- B.Sc Life Sciences
- M.Sc Life Sciences
- Biotechnology
- Clinical Research
- Health Sciences
- Information Technology
- Related Life Science Degree
Preferred Skills
- SAS Programming
- Medidata Rave
- Oracle InForm
- Clinical Data Management
- CDISC Standards
- CRF Design
- Database Programming
- Clinical Trial Data
- Excel
- Spotfire
- R Programming
- Data Reconciliation
2. Clinical Research Associate (CRA)
Company: Fortrea
Job Location: Bangalore, India
Employment Type: Full-Time
Experience Required: Minimum 2 Years Clinical Monitoring
Key Responsibilities
- Conduct Site Selection, Initiation, Monitoring, and Close-Out Visits.
- Perform Source Data Verification (SDV).
- Review informed consent documentation.
- Generate and resolve study queries.
- Monitor protocol compliance.
- Review Serious Adverse Events (SAEs).
- Maintain Trial Master File (TMF/eTMF) documentation.
- Ensure audit readiness at clinical sites.
- Coordinate with investigators and sponsor teams.
- Prepare monitoring reports.
- Track Investigational Product accountability.
- Support investigator meetings and site training.
- Travel to study sites (approximately 60%).
Required Qualifications
Eligible candidates may have:
- B.Pharm
- M.Pharm
- Pharm.D
- B.Sc Nursing
- M.Sc Nursing
- MBBS
- BDS
- Life Sciences
- Allied Health Sciences
Preferred Skills
- Clinical Monitoring
- ICH-GCP
- Clinical Operations
- Site Management
- CTMS
- SAE Reporting
- Clinical Trial Monitoring
- SDV
- eCRF Review
- Regulatory Documentation
- TMF/eTMF
- Clinical Research
Why Join Fortrea?
Fortrea is recognized globally for delivering clinical development services across multiple therapeutic areas. Employees benefit from:
- Global CRO exposure
- International clinical trials
- Career advancement opportunities
- Exposure to leading pharmaceutical sponsors
- Structured learning and development
- Collaborative work culture
- Competitive compensation
- Modern clinical technology platforms
Who Should Apply?
These Fortrea opportunities are ideal for professionals with experience in:
- Clinical Data Management
- SAS Programming
- Clinical Database Programming
- Medidata Rave
- Oracle InForm
- Clinical Monitoring
- Clinical Research
- CRO Operations
- Pharmacovigilance professionals transitioning into Clinical Research
How to Apply
Application Link For Programmer
Application Link For Clinical Research Associate II
