Company:A Large Global Organization
Key Skills: Clinical Research, Ophthalmology, Optometry, Vision Science, Clinical Data Management, Clinical Study Documentation, Clinical Protocol Development, IRB Submissions, Clinical Trial Registration, Scientific Reporting
Roles & Responsibilities:
• Write clinical study protocols aligned to scientific objectives and study design requirements.
• Support study documentation including source forms and case report forms.
• Prepare and manage IRB submissions and clinical trial registration materials.
• Review, organize, and summarize clinical study data for analysis and reporting.
• Draft study reports and scientific summaries with attention to data integrity and regulatory compliance.

Experience:




• 8 to 13 years of relevant clinical research experience in ophthalmology, optometry, or vision science.
• Solid background in ophthalmology, optometry, and vision science clinical research.
• Experience writing clinical study protocols and supporting study documentation.
• Ability to manage clinical data review, analysis support, and study reporting workflows.
• Experience with clinical research submissions and regulated study environments.

Good to Have:
• Experience preparing manuscripts, abstracts, posters, or scientific presentations.

Education:
• B.Sc. in Optometry or related field; advanced degree preferred.

📌 Principal Clinical Project Lead (Bengaluru)
🏢 MyCareernet
📍 Bengaluru