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Director, Clinical Projects, Vision Care

Alcon
flex time
Mar 27, 2025

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.

We foster an inclusive culture and are looking for diverse, talented people to join Alcon. As a Director, Clinical Projects, Vision Care supporting the U.S. Clinical Research Development Team, in Duluth, GA, a typical day will include:

  • Lead and manage R&D Clinical Project Leads to develop high quality global medical evidence plans, pre & post registration (Phase I - IV) in all stages of the medical device development, for the specific product area(s) in the device pipeline in full alignment with the Franchise imperatives

  • Accountable for ensuring high-quality, scientifically-sound clinical protocols and related documents that produce clear, decisive results.

  • Lead and matrix manage the clinical trial aspect for project/program teams to ensure all trial deliverables are met according to timelines, budget, quality standards and operational procedures, report study progress and issues with their resolution plan.

  • Accountable for medical/scientific review of clinical trial data, final analysis, and interpretation within clinical trial reports, publications, and internal/external oral and written presentations.

  • Accountable for developing realistic trial budget forecasts and for timely execution of clinical studies and for the reallocation of resources as required to meet targets.

  • Forecast trial resource needs (headcount and external costs): accountable for the development, management and tracking of trial budget. Accountable for accuracy of trial information in all trial databases and tracking systems. Assess resource needs with program to ensure appropriate line function allocation.

  • Contribute to the development of clinical sections of regulatory documents like Investigators' Brochures, briefing books, safety updates, regulatory submission documents, and responses to Health Authorities questions.

  • Participate in the on-boarding and training of new Clinical R&D staff and for mentoring new project/program team members as needed.

  • Responsible for post marketing studies, and training of customer facing medical affairs associates worldwide

  • Stay abreast of relevant literature and clinical practice norms for the project/program area(s)

  • Contribute as SME to life cycle Management, Clinical evaluation, development of post market clinical studies, surveys to support OUS submissions and registrations

WHAT YOU'LL BRING TO ALCON:

  • Bachelor's Degree or Equivalent years of directly related experience (or high school +18 yrs; Assoc.+14 yrs; M.S.+7 yrs; PhD+6 yrs)

  • The ability to fluently read, write, understand and communicate in English

  • 10 Years of Relevant Experience

  • Work hours:40 hours

  • Travel: 20%

  • Relocation: Yes

  • Sponsorship Assistance: Yes

HOW YOU CAN THRIVE:

  • Collaborate with teammates to share standard processes and findings as work evolves

  • See your career like never before with focused growth and development opportunities

  • Join Alcon's mission to provide outstanding, innovative products and solutions to improve sight, improve lives, and grow your career!

  • Alcon provides robust benefits package including health, life, retirement, flexible time off and much more.

Alcon Careers

See your impact at alcon.com/careers

ATTENTION: Current Alcon Employee/Contingent Worker

If you are currently an active employee/contingent worker at Alcon, please click the appropriate link below to apply on the Internal Career site.

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Alcon is an Equal Opportunity Employer and participates in E-Verify. Alcon takes pride in maintaining a diverse environment and our policies are not to discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, gender identity, marital or veteran status, disability, or any other legally protected status. Alcon is also committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please send an email to alcon.recruitment@alcon.com and let us know the nature of your request and your contact information.

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