Fortrea is hiring for the position of Lead Safety Systems Specialist in Bangalore, India. This is a full-time opportunity for professionals with experience in drug safety systems, pharmacovigilance technology, system operations and validated safety platforms.
The role focuses on supporting the implementation, configuration, migration and ongoing operation of safety systems for internal and external clients. The position combines business understanding with technical expertise and involves working with systems such as Argus, ARISg and Veeva.
Candidates with at least 4 years of experience working with drug safety systems, along with experience in system operations support, validated systems and system integration, may be suitable for this opportunity.
Fortrea Recruitment 2026 – Job Highlights
| Job Details | Information |
|---|---|
| Company | Fortrea |
| Job Position | Lead Safety Systems Specialist |
| Job Requisition ID | 265203 |
| Job Location | Bangalore, India |
| Employment Type | Full-Time |
| Work Environment | Office or Remote |
| Qualification | Life Science or IT/Computing Degree |
| Drug Safety Systems Experience | At least 4 Years |
| Key Systems | Argus, ARISg, Veeva |
| Industry | Clinical Research / Pharmacovigilance |
| Application Mode | Online |
| Closing Date | 31 October 2026 |
About Fortrea
Fortrea is a global clinical research services organization supporting pharmaceutical, biotechnology and healthcare companies in clinical development.
The Lead Safety Systems Specialist position supports the technology and systems used for Pharmacovigilance and drug safety operations. The role works across technical, functional and business requirements to help maintain quality, compliance and efficiency in safety system processes.
Job Description
Lead Safety Systems Specialist
The Lead Safety Systems Specialist will support the implementation, configuration, migration and operation of safety systems used for Pharmacovigilance activities.
The professional will work as a subject matter expert by combining technical knowledge with an understanding of drug safety processes. Responsibilities include system configuration, reporting, data extraction, migration support, issue resolution, user support, training, testing and continuous process improvement.
The role also requires collaboration with business stakeholders, technology partners, vendors and internal teams to ensure system requirements are understood and delivered appropriately.
Eligibility Criteria
Educational Qualification
Candidates should have:
- A degree in Life Sciences, or
- A degree in IT / Computing.
Fortrea may consider relevant and equivalent professional experience in place of the stated educational requirements.
Experience Requirements
Candidates should have:
- Experience working in a systems operations support role.
- Experience with validated document management systems.
- At least 4 years of experience with drug safety systems, such as:
- Argus
- ARISg
- Veeva
- Experience with Microsoft Office tools.
- Knowledge of system integration.
Preferred Qualifications
The following experience can be advantageous:
- Clinical background involving clinical systems.
- Working knowledge of SQL.
- Experience with ticket management or ticket support applications.
- Experience supporting validated systems.
- Understanding of Pharmacovigilance technology and workflows.
Key Skills
- Pharmacovigilance Systems
- Drug Safety Systems
- Argus Safety
- ARISg
- Veeva
- Safety System Configuration
- System Implementation
- System Migration
- System Operations Support
- System Integration
- Data Extraction
- Safety Reporting
- MedDRA
- Standard MedDRA Queries (SMQ)
- SQL
- User Acceptance Testing
- Ticket Management
- Issue Resolution
- Vendor Management
- Change Management
- Technical Documentation
- SOP Management
- Microsoft Office
- Training and User Support
Key Responsibilities
The selected Lead Safety Systems Specialist will be responsible for a wide range of technical and functional activities.
Safety System Configuration
- Support implementation and configuration activities for Pharmacovigilance safety systems.
- Perform project-specific system configurations based on business requirements.
- Maintain documentation for system configuration and subsequent changes.
- Evaluate proposed software changes through technical impact assessments.
- Consider the potential business value of proposed system changes when supporting decision-making.
Reporting and Data Extraction
- Develop standard and ad hoc reports from safety systems.
- Support front-end reporting using standard safety system functionality.
- Provide guidance on advanced conditions and Standard MedDRA Queries (SMQs).
- Perform routine and ad hoc data extraction.
- Support data requirements for safety reports and listings, including activities related to PSURs, DSURs and six-monthly listings.
Business Requirements and System Delivery
- Work with business stakeholders to understand system requirements.
- Document user requirements accurately.
- Coordinate with technology partners to support timely delivery of requirements.
- Help ensure system solutions meet agreed business needs.
- Participate in technical and functional discussions related to system improvements.
Data Migration
- Participate actively in safety system data migration activities.
- Support migration planning and execution.
- Maintain appropriate documentation associated with migration activities.
- Assist with validation and related processes where required.
User Support and Training
- Provide support to end users and sponsors where applicable.
- Respond to system-related queries received through designated mailboxes.
- Monitor system-related mailbox requests and failures.
- Work with training teams to develop safety system-specific training modules.
- Train team members on technical and functional aspects of safety systems.
- Support change management and user training activities.
Issue and Ticket Management
- Manage tickets related to safety system issues.
- Investigate and support resolution of system problems.
- Escalate issues to appropriate teams when required.
- Monitor system failure notifications and work toward timely resolution.
- Maintain communication with relevant stakeholders during issue resolution.
Testing and Quality
- Perform User Acceptance Testing (UAT).
- Complete required testing documentation.
- Ensure work is completed according to relevant SOPs and quality standards.
- Support compliance, data quality and operational efficiency.
- Keep knowledge current regarding applicable Pharmacovigilance regulations.
SOPs and Process Improvement
- Update departmental SOPs when required.
- Contribute to Working Practices and Guidelines.
- Identify opportunities to improve compliance, quality and efficiency.
- Act as a subject matter expert for relevant safety system processes.
Project and Team Leadership
- Lead critical team projects when assigned.
- Help manage and prioritize team workload.
- Provide peer support and technical guidance.
- Coordinate with internal teams, vendors and other business partners.
Pharmacovigilance Systems Expertise
A major component of this position is expertise in drug safety technology. Candidates should have hands-on experience with at least one major safety system, with the vacancy specifically identifying Argus, ARISg and Veeva.
Experience with validated systems, system integration, configuration, reporting, migration and user support is particularly relevant to the role.
Work Location and Environment
The position is based in Bangalore, India.
The provided vacancy describes the work environment as:
- Office environment, or
- Remote
The specific working arrangement for an individual candidate should be confirmed during the recruitment process.
Salary / CTC
The salary or CTC for the Lead Safety Systems Specialist position has not been disclosed in the provided vacancy information.
Candidates should confirm compensation and other employment terms directly through the Fortrea recruitment process.
Selection Process
The detailed selection process has not been specified in the provided job description.
Candidates whose qualifications and experience match the requirements may be contacted by Fortrea for subsequent recruitment stages.
How to Apply
Interested and eligible candidates can apply online through the official Fortrea careers portal.
Application Details
- Job Title: Lead Safety Systems Specialist
- Job Requisition ID: 265203
- Location: Bangalore, India
- Employment: Full-Time
- Closing Date: 31 October 2026
Candidates should ensure that their resume clearly highlights relevant drug safety systems, Pharmacovigilance technology, system operations, configuration, migration, integration and technical support experience.
Important Details Before Applying
- Company: Fortrea
- Position: Lead Safety Systems Specialist
- Job ID: 265203
- Location: Bangalore, India
- Employment: Full-Time
- Work Environment: Office or Remote
- Qualification: Life Science or IT/Computing Degree
- Drug Safety Systems Experience: At least 4 years
- Systems: Argus, ARISg, Veeva
- Preferred: SQL and ticket support application experience
- Core Area: Pharmacovigilance Safety Systems
- Salary: Not disclosed
- Application: Online
- Last Date: 31 October 2026
Frequently Asked Questions
1. What position is Fortrea hiring for?
Fortrea is hiring for a Lead Safety Systems Specialist.
2. Where is this Fortrea job located?
The position is based in Bangalore, India.
3. What qualification is required?
A degree in Life Sciences or IT/Computing is required. Fortrea may consider relevant equivalent experience in place of educational requirements.
4. How much experience is required with drug safety systems?
The vacancy requires at least 4 years of experience with drug safety systems such as Argus, ARISg or Veeva.
5. Is Argus experience relevant to this position?
Yes. Argus is specifically listed among the drug safety systems relevant to the role.
6. Is SQL knowledge required?
SQL is listed under preferred qualifications, so working knowledge of SQL can be advantageous.
7. What are the main responsibilities of this role?
The role covers safety system configuration, implementation, migration, reporting, data extraction, user support, issue resolution, training, UAT, documentation, vendor coordination and process improvement.
8. Can this role be remote?
The provided job description lists the work environment as office or remote. The applicable arrangement should be confirmed during recruitment.
9. Is salary mentioned?
No. The salary or CTC has not been disclosed in the provided vacancy information.
10. What is the last date to apply?
The vacancy lists 31 October 2026 as the closing date.
Important Note
Recruitment requirements, vacancy status, application deadlines, work arrangements, compensation and other employment conditions may be updated by Fortrea. Candidates should verify the latest information on the official Fortrea careers portal before applying. Meeting the stated requirements does not guarantee selection.