Principal I, Clinical Project Lead

Key Responsibilities:

This position would be on-site in Bangalore, India and a typical day would include:

• Writing clinical research study protocols and ensuring the study design meets the scientific objectives and includes an appropriate statistical analysis plan.
• Creating or supporting design of study source forms and case report forms as required by each project.
• Assisting with Clinical Trial Registrations and IRB submissions.
• Processing, reviewing, and organizing clinical data and records, ensuring accuracy, consistency, and timely availability for analysis and reporting.
• Reviewing and critically analyzing scientific data from clinical studies.
• Writing study reports ensuring data integrity, scientific rigor, and regulatory compliance.
• Supporting/contributing to peer‑reviewed publications, abstracts, posters, and presentations.
• Compiling competitive intelligence (CI) from optometry, ophthalmology and vision science conferences, scientific literature, ophthalmology journals, and internal CI sources.
• Critically reviewing, analyzing, and summarizing scientific data from published literature.
• Preparing narrative summaries, literature reviews, and scientific slide decks on topics of interest.
• Adhering to all GxP requirements by following SOPs, maintaining complete documentation, performing quality-controlled work, and completing all required training.

Key Requirements/Minimum Qualifications:

• Bachelor’s Degree or Equivalent years of directly related experience in clinical research in Ophthalmology/Optometry/Vision Science.
• Experience in planning, conducting, and reporting of clinical studies in medical ophthalmic devices.
• The ability to fluently read, write, understand, and communicate in English.

Preferred Qualifications:

• Advanced Degree in Optometry/Ophthalmology/Vision Science (OD, MD, Masters, PhD in Vision Science) or related field.
• Experience in conducting prior research with industry and/or developing novel clinical endpoints in vision science/physiological optics.
• Experience in writing clinical study protocols.
• Experience in planning, conducting, and reporting clinical research in vision science.
• Experience in clinical trials regulations such as GCP and ISO standards.
• Experience in the field of vision science, physiological optics, binocular vision/accommodation, intraocular lenses, contact lenses.

Work hours: 1 PM to 10 PM IST

Relocation assistance: Yes

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