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Fortrea Hiring Regulatory and Start-Up | Clinical Research & Site Start-Up Careers
🏢 Fortrea
📍 Bangalore
📄 Regulatory and Start-Up
💼 3–5 Years Experience
Fortrea, a leading global Contract Research Organization (CRO), is hiring experienced professionals for its Regulatory and Start-Up team in Bangalore. This role is ideal for candidates with experience in Clinical Trial Agreements (CTA), Site Start-Up Activities, Regulatory Affairs, Contract Negotiation, and Clinical Operations.
Professionals seeking career growth in Regulatory Affairs, Clinical Research Operations, Study Start-Up, Contract Management, and CRO environments are encouraged to apply.
📋 Job Overview
| Details | Information |
|---|---|
| Position | Regulatory and Start-Up |
| Company | Fortrea |
| Location | Bangalore, Karnataka |
| Experience | 3–5 Years |
| Qualification | Life Sciences / Pharmacy / Clinical Research |
| Industry | Clinical Research (CRO) |
| Employment Type | Full-Time |
| Application Deadline | 31 July 2026 |
💰 Expected Salary Range: ₹6 LPA – ₹12 LPA
🏢 About Fortrea
Fortrea is a globally recognized Clinical Research Organization delivering clinical development and patient access solutions across multiple therapeutic areas. The company partners with pharmaceutical, biotechnology, and medical device organizations worldwide.
📌 Clinical Trial Contract Management Responsibilities
- Draft, review, negotiate, and finalize Clinical Trial Agreements (CTAs).
- Prepare confidentiality agreements, amendments, and related contracts.
- Coordinate with sponsors, legal teams, and study teams.
- Ensure timely contract execution aligned with study milestones.
- Manage contract approval workflows and documentation.
- Track contract status and maintain regulatory records.
- Identify contracting risks and escalate issues when required.
📌 Protocol Amendment & Start-Up Responsibilities
- Coordinate protocol amendment submissions.
- Support amendment-related budget and contract revisions.
- Communicate timelines and requirements to study teams.
- Track amendment progress and approvals.
- Collaborate with Regulatory, Legal, Clinical Operations, and Finance teams.
- Maintain study trackers and amendment documentation.
- Support site activation and start-up activities.
🎓 Eligibility Criteria
- B.Pharm
- M.Pharm
- Life Sciences
- Biotechnology
- Clinical Research
- Microbiology
- Biochemistry
- Nursing
- Medical Technology
- Laboratory Technology
- Related Allied Health Disciplines
Experience Required:
- Minimum 3–5 Years Clinical Research Experience.
- Clinical Trial Agreements (CTA) Experience Preferred.
- Site Start-Up & Regulatory Activities Experience.
- CRO Industry Experience Preferred.
💡 Required Skills
- Clinical Trial Agreements (CTA)
- Site Start-Up Activities
- Regulatory Affairs
- Protocol Amendments
- Contract Negotiation
- Clinical Operations
- ICH-GCP Compliance
- Clinical Research Documentation
- Stakeholder Management
- Microsoft Office Suite
- Cross-Functional Collaboration
- Regulatory Submissions
🎁 Why Join Fortrea?
- Global clinical research exposure.
- Career advancement opportunities.
- Cross-functional collaboration with global teams.
- International project experience.
- Competitive compensation packages.
- Professional development programs.
- Flexible and inclusive work culture.
- Opportunity to work on large-scale global clinical trials.
👨🔬 Who Should Apply?
- Clinical Research Associates (CRAs)
- Site Start-Up Specialists
- Regulatory Affairs Associates
- Clinical Trial Coordinators
- Contract Specialists
- TMF Professionals
- Clinical Operations Professionals
- Life Sciences Graduates with Relevant CRO Experience
📄 Resume & Interview Preparation Tips
- Highlight CTA drafting, review, and negotiation experience.
- Mention Site Start-Up, Regulatory Affairs, and Protocol Amendment activities.
- Showcase ICH-GCP knowledge and Clinical Operations experience.
- Include sponsor interaction, contract management, and CRO exposure.
- Keep your resume ATS-friendly and achievement-focused.
📚 Clinical Research Resources
👉 Clinical Research Coordinator Career Guide
👉 CRA Knowledge Quiz
👉 Clinical Trial Assistant Quiz
📝 How to Apply
- Read the complete job description carefully.
- Prepare an updated ATS-friendly resume.
- Highlight CTA, Site Start-Up, Regulatory Affairs, and Clinical Operations experience.
- Complete the 15-second countdown timer to unlock the application button.
- Apply before the application deadline.
⏰ Application Deadline: 31 July 2026
🚀 Job Application Link
📌 Last Date to Apply: 31 July 2026
Please make sure to read the complete job description, eligibility criteria, and skills required carefully before submitting your application. Aligning your resume with the specific role requirements significantly increases your chances of getting shortlisted by recruiters.
Please make sure to read the complete job description, eligibility criteria, and skills required carefully before submitting your application. Aligning your resume with the specific role requirements significantly increases your chances of getting shortlisted by recruiters.
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