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.

Valuable 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 Clinical Research & Development Bengaluru (India)
🏢 MyCareernet
📍 India