New · posted Nov 1
Alcon · Medical Devices
Sr. Principal I, Clinical Project Management
- Fort Worth, TX
- On-site
- Full-time
- Senior & Principal
The role
This is an onsite position based out of our Fort Worth, TX Main Campus Or Lake Forest, CA Main Campus
At Alcon, we're passionate about enhancing sight and helping people see brilliantly. With more than 25,000 associates, we innovate fearlessly, champion progress, and act swiftly to impact global eye health. We foster an inclusive culture, recognizing your contributions and offering opportunities to grow your career like never before. Together, we make a difference in the lives of our patients and customers. Are you ready to join us?
This role is part of Alcon's Project Management function, a team that ensures all regular and one-off projects are planned, organized, and executed effectively to help our people and the world see brilliantly. The Sr. Principal II, Clinical Project Management, is primarily responsible for serving as a global/regional clinical expert throughout the product lifecycle, from development to post-market monitoring. You will build effective relationships across teams, implement clinical strategies, and ensure compliance with protocols.
What you need
WHAT YOU’LL BRING TO ALCON
· Bachelor’s Degree or Equivalent years of directly related experience (or high school+15 yrs. Assoc.+11 yrs.; M.S.+4 yrs.; PhD+3 yrs.)
· The ability to fluently read, write, understand, and communicate in English
· 7 Years of Relevant Experience
Preferrednice to have
·Ophthalmology experience (Glaucoma Preferred)
What you'll do
In this role, a typical day will include
·Leading projects leveraging clinical data and developing clinical content
·Implementing and preparing the clinical development strategy as outlined by the clinical sub-teams or workstreams
·Gathering input from cross-functional teams and creating plans that help the team produce deliverables on schedule
·Planning, directing, creating, and communicating clinical study timelines
·Ensuring consistency of clinical study and processes across clinical trials
·Ensuring study is conducted within clinical trial protocols
·Monitoring progress and following up with team members and line managers when issues develop
·Overseeing and resolving operational aspects of clinical trials in conjunction with project teams and in accordance with standard operating procedures (SOP), good clinical practice (GCP) and specific country regulations
·Participating in data analysis, interpretation and synthesis, instruction in order to develop Clinical study report and /or support development of scientific publications including peer reviewed manuscripts in partnership with external key opinion leaders (KOLs)
Pay
Alcon didn't publish pay for this role
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· 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 a robust benefits package including health, life, retirement, flexible time off and much more.
Where you'll work
Fort Worth, TXOn-siteOpen in Maps (opens in a new tab)
More jobs in Fort Worth, TXWorking conditions
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.
From the posting
About Alcon
Other
·Travel Requirements: up to 20% International and/or Domestic
Equal opportunity, accessibility and legal noticesAlcon's statements, word for word
ALCON IS AN EQUAL OPPORTUNITY EMPLOYER AND PARTICIPATES IN E-VERIFY
Alcon takes pride in maintaining an inclusive environment that values different perspectives and our policies are non-discriminatory in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, 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 [email protected] and let us know the nature of your request and your contact information.
Job intelligence
The context around this role
Live data · November 1, 2026
Career trajectory
Where this role sits in Clinical Project Management
The general path across 37 open Clinical Project Management roles on Regulatory Jobs, with the titles they carry most. Not Alcon's own promotion track.
Skills DNA
What this role leans on
How many of the posting's 15 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- Clinical trial conduct7
- Collaboration and leadership7
- GMP and compliance2
- Documentation and SOPs2
Regulatory intelligence
The rules behind this role
Frameworks and standards this posting's work falls under, matched from its own words, each linked to the official source.
Company hiring pulse
Alcon on Regulatory Jobs
- 16
- Open roles
- 15
- Distinct roles
- 5
- Locations
By discipline
- Quality13 81%
- Regulatory2 13%
- Clinical1 6%
By level
- Associate & Specialist6 38%
- Senior & Principal4 25%
- Director3 19%
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Sr. Principal I, Clinical Project Management at Alcon
Applications close December 7.