Looking to build a career in Regulatory Affairs, Clinical Trial Transparency, and Disclosure? Here’s a high-impact opportunity with Roche, a global leader in pharmaceuticals and diagnostics. This role sits at the intersection of clinical research, regulatory compliance, and global health authority reporting, making it ideal for professionals with experience in regulatory writing and clinical trial disclosure.

This position plays a critical role in ensuring compliance with global clinical trial transparency requirements, including registries like ClinicalTrials.gov and EU CTR, while supporting Roche’s mission of improving patient access to healthcare.

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📌 Job Overview

• Role: Clinical Trial Transparency and Disclosure Specialist
• Company: Roche India (Roche Services & Solutions)
• Location: Hyderabad / Chennai
• Experience: 4+ years
• Employment Type: Full-time
• Last Date to Apply: April 15, 2026

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💼 Key Responsibilities

As a Clinical Trial Disclosure Specialist, you will:

• Act as a Subject Matter Expert (SME) in regulatory and product development lifecycle
• Manage clinical trial disclosure and transparency activities
• Post clinical trial data on registries (e.g., ClinicalTrials.gov, EU CTR)
• Ensure compliance with GCP, ICH, and GxP guidelines
• Perform quality checks on protocol submissions and registry data
• Collaborate with cross-functional teams for data collection and approvals
• Track timelines and ensure on-time regulatory submissions
• Monitor workflows and manage regulatory documentation consistency
• Handle communication across global stakeholders and affiliates

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🎓 Qualifications & Skills

✅ Educational Requirements:

• Bachelor’s / Master’s / Pharm.D in:
  • Life Sciences
  • Pharmacy
  • Clinical Research

✅ Experience:

• Minimum 4+ years in Regulatory Affairs / Regulatory Writing
• Exposure to clinical trial disclosure & product development lifecycle

✅ Key Skills:

• Strong knowledge of:
  • GCP, ICH, GxP guidelines
  • Clinical trial registries & disclosure requirements
• Proficiency in:
  • Microsoft Office, Google Suite, Adobe Acrobat
• Excellent:
  • Communication & stakeholder management
  • Project planning & time management

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🎁 Benefits of Working at Roche

• 🌍 Work with a global healthcare leader
• 🤝 Collaborative and innovation-driven culture
• 📈 Strong career growth in Regulatory Affairs & Clinical Development
• 🧠 Exposure to global regulatory frameworks and compliance systems
• 💼 Opportunity to work in a matrix-based international environment

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📩 How to Apply

Application Link