Fortrea, a leading global Contract Research Organization (CRO), is hiring for the Regulatory and Start-Up role in Bangalore, India.
This is a great opportunity for professionals with 3–5 years of clinical research experience to grow in regulatory affairs, site start-up, and clinical trial operations.
About Fortrea
Fortrea is a globally recognized CRO delivering end-to-end clinical development solutions across multiple therapeutic areas.
The company offers:
- Global clinical trial exposure
- International project collaboration
- Strong regulatory and compliance framework
- Career growth in clinical research
Job Overview
| Particular | Details |
|---|---|
| Position | Regulatory and Start-Up |
| Company | Fortrea |
| Location | Bangalore, India |
| Experience | 3–5 Years |
| Qualification | Life Sciences / Pharmacy / Biotechnology / Clinical Research |
| Industry | Clinical Research (CRO) |
| Employment Type | Full-Time |
| Deadline | July 31, 2026 |
Eligibility Criteria
Candidates should have:
- Bachelor’s or Master’s degree in:
- Life Sciences
- Pharmacy
- Biotechnology
- Clinical Research
- Microbiology / Biochemistry
- 3–5 years of experience in clinical research or CRO
- Knowledge of:
- ICH-GCP guidelines
- Clinical trial agreements (CTAs)
- Regulatory processes
Key Skills Required
- Clinical Trial Agreements (CTA)
- Site Start-Up Activities
- Regulatory Affairs
- Protocol Amendments
- Contract Negotiation
- Clinical Documentation
- Stakeholder Management
- Compliance & Quality
Roles & Responsibilities
Clinical Trial Contract Management
- Draft and negotiate Clinical Trial Agreements (CTAs)
- Manage confidentiality agreements and amendments
- Coordinate with sponsors, legal, and study teams
- Track contract status and approvals
Protocol Amendment Management
- Handle protocol amendment submissions
- Support budget and contract revisions
- Track approvals and timelines
- Communicate updates to stakeholders
Compliance & Quality
- Ensure adherence to ICH-GCP and SOPs
- Maintain audit-ready documentation
- Support process improvements
- Deliver reports and study metrics
Experience Required
- 3–5 years in clinical research
- Experience in:
- Site start-up
- Contract management
- Regulatory activities
- Exposure to sponsor and cross-functional coordination
Benefits & Perks
- Competitive salary package
- Global project exposure
- Career advancement opportunities
- Cross-functional collaboration
- Professional development programs
- Inclusive and flexible work culture
Who Should Apply?
- Clinical Research Associates (CRAs)
- Site Start-Up Specialists
- Regulatory Affairs Associates
- Clinical Trial Coordinators
- Contract/CTA Specialists
- TMF professionals transitioning to start-up roles
How to Apply
👉 Apply through the official Fortrea careers portal (online application)
Why Join Fortrea?
- Work with a global CRO leader
- Exposure to international clinical trials
- Strong career growth in regulatory & start-up
- Opportunity to collaborate with global teams
- Enhance expertise in clinical trial operations
FAQs
1. What experience is required?
3–5 years in clinical research or CRO roles.
2. What is the job location?
Bangalore, India
3. What skills are important?
CTA, regulatory affairs, site start-up, ICH-GCP.
4. What is the application deadline?
July 31, 2026
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