Clinical Applications Specialist - Chicago at Alcon
Illinois, Illinois, USA -
Full Time


Start Date

Immediate

Expiry Date

22 Oct, 25

Salary

0.0

Posted On

23 Jul, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Patient Outcomes, Research, Clinical Support, Adverse Events, Knowledge Sharing, Operational Excellence, Continuous Process Improvement

Industry

Pharmaceuticals

Description

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 Sales & Sales Support function, a team that helps provide access to products across all channels in an effort to drive customer satisfaction with eye care professionals to help people see brilliantly.

The Sr. Associate I, Clinical Applications Services & Support (Professional Path) is primarily responsible for training customers on the safe and effective use of Alcon products to ensure optimal patient outcomes. You will drive operational excellence through process improvement and knowledge sharing, ensuring all trial deliverables meet timelines, budgets, and quality standards. Specifics include:

  • Train operating room staff on Alcon products
  • Provide on-site and remote clinical support and technical information
  • Implement equipment and software upgrades at clinical sites
  • Respond to customer inquiries per standard operating procedures and guidelines
  • Attend and support medical events and demonstrations
  • Collaborate with Field Service Engineers and Sales Representatives for installations and support
  • Provide constant feedback to Research and Development on clinical performance of products via an approved communication plan
  • Document site visits within 48 hours
  • Report and address adverse events and device deficiencies, and refer unapproved use inquiries
  • Achieve required clinical certifications
  • Promote and advocate for continuous process improvement and operational excellence through knowledge sharing

All associates must adhere to GxP regulations by strictly following Standard Operating Procedures (SOPs), maintaining accurate and complete documentation, ensuring rigorous quality control, and completing all required training. Associates are responsible for meeting their individual job requirements and contributing to the overall compliance of the organization. Compliance with regulatory requirements and a commitment to continuous improvement are essential to our operations.

What you will bring to Alcon:

  • Bachelor’s Degree or Equivalent years of directly related experience (or high school +10 yrs; Assoc.+6 yrs; M.S.+0 yrs)
  • The ability to fluently read, write, understand, and communicate in English.
  • 2 Years of Relevant Experience
  • Work hours: Full time
  • Travel Requirements: 85%%

JCAHPO certification and experience in an ophthalmic environment is required
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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Responsibilities
  • Train operating room staff on Alcon products
  • Provide on-site and remote clinical support and technical information
  • Implement equipment and software upgrades at clinical sites
  • Respond to customer inquiries per standard operating procedures and guidelines
  • Attend and support medical events and demonstrations
  • Collaborate with Field Service Engineers and Sales Representatives for installations and support
  • Provide constant feedback to Research and Development on clinical performance of products via an approved communication plan
  • Document site visits within 48 hours
  • Report and address adverse events and device deficiencies, and refer unapproved use inquiries
  • Achieve required clinical certifications
  • Promote and advocate for continuous process improvement and operational excellence through knowledge sharin
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