Are you looking to grow your career in clinical research and regulatory documentation? ICON plc — a global leader in healthcare intelligence and clinical development — is hiring a Clinical Document Specialist in India (Remote).
This role is an excellent opportunity for candidates with experience in clinical documentation, ICH-GCP compliance, regulatory submission processes, and document lifecycle management.
If you want to build a strong career in the pharmaceutical, biotechnology, or CRO industry, this opening may be the right next step.
🧪 Role: Clinical Document Specialist
📍 Location: Remote (India)
🕒 Job Type: Full-Time
📌 Key Responsibilities
As a Clinical Document Specialist at ICON, you will:
- Manage, collect, review, and maintain essential trial documentation
- Ensure compliance with ICH-GCP, FDA, and regulatory standards
- Coordinate and track documentation across study lifecycle
- Support internal and external audits with documentation accuracy
- Collaborate cross-functionally to solve document gaps or compliance issues
- Assist in improving SOPs and document management workflows
🎓 Qualifications Required
To qualify, you should have:
✔ Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, or relevant field
✔ Experience in clinical research, regulatory affairs, or clinical document management
✔ Strong knowledge of clinical trial documentation guidelines and quality systems
✔ Excellent communication, time management, and organizational skills
Candidates with CRO or pharmaceutical documentation experience are preferred.
🎯 Why Join ICON?
ICON offers:
- Competitive salary and career progression
- Remote flexibility and global exposure
- Health insurance and employee wellbeing benefits
- Annual leave, retirement benefits, and professional support programs
- Inclusive culture with equal growth opportunities
📝 How to Apply
