Principal I, Clinical Project Lead

Alcon; Bengaluru; On-site; INR 1,500,000 - 2,100,000; Full time

Benefits offered by this job

Relocation assistance

Job summary

Alcon is seeking a Principal I, Clinical Project Lead to join the Clinical Research & Development CoE in Bengaluru. You will drive innovation in vision science and translate bench findings into clinically meaningful outcomes across portfolios, coordinating study design, data collection, analysis, and publication efforts.

The role requires a foundation in visual optics/vision science and experience in planning, conducting, and reporting clinical studies in ophthalmic devices.

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.

Responsibilities

• Write clinical research study protocols and ensure the study design meets objectives with a suitable statistical analysis plan.
• Design or support study source forms and case report forms for projects.
• Assist with Clinical Trial Registrations and IRB submissions.
• Process, review, and organize clinical data for analysis and reporting.
• Review and critically analyze scientific data from clinical studies.
• Write study reports ensuring data integrity and regulatory compliance.
• Support/contribute to peer-reviewed publications, abstracts, posters, and presentations.
• Compile competitive intelligence (CI) from ophthalmology and vision science sources.
• Critically review and summarize scientific literature.
• Prepare narrative summaries and literature reviews and scientific slides on topics of interest.
• Adhere to GxP requirements by following SOPs and maintaining documentation.

Skills

Clinical research

Ophthalmology/Optometry

Data analysis

Education

Bachelor’s Degree in relevant field

Advanced Degree in Vision Science/Optometry/Ophthalmology

Job description

Summary of Position

At Alcon, we are driven by the meaningful work we do to help people see brilliantly. We innovate boldly, champion progress, and act with speed as the global leader in eye care. Here, you’ll be recognized for your commitment and contributions and see your career like never before. Together, we go above and beyond to make an impact in the lives of our patients and customers.

The role of Principal I, Clinical Project Lead will be part of the Clinical Research & Development Center of Excellence (CoE), driving innovation and excellence in vision science and optometry/ophthalmology to advance the company’s pipeline. The projects in this role will support expansion of our vision science capabilities by focusing on novel endpoints and translation of bench-based innovations into clinically meaningful outcomes that will drive product differentiation and patient impact that will span across many portfolios within Alcon. The ideal candidate will have foundational knowledge in visual optics/vision science and clinical research. They will be responsible for document creation, planning, analyzing, reporting on clinical studies and collating results for impactful peer reviewed publications/presentations aimed at increasing share of voice for Alcon.

Key Responsibilities

• 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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