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 Research & Development function, a team that innovates boldly and delivers new products and services to help revolutionize the eye care industry, advance optimal patient outcomes and help people see brilliantly.

For the Principal Medical Writer position, you will be able to work remotely and you will be accountable for all clinical writing aspects of assigned clinical trials and projects, author robust reports, summaries, and regulatory documents with scientific rigor and quality, including device and/or pharma CSRs, plain language and other summaries, and submission modules (i.e., NDA), manage and author relevant sections of any IB with scientific rigor and quality and ensure that all writing is completed with quality and timeliness

In this role, a typical day will include:

Each Medical Writer Lead will represent Clinical Writing on up to 8 CTTs at one time for studies of medium to high complexity.

Responsible for the timely review of the protocol, MOP, and TFL shells and dry runs for studies of all levels of complexity

Responsible for the timely delivery of IBs (regardless of complexity)

Responsible for independently authoring various summaries, CSRs, and other reports

Manages the authoring, review, and approval of IBs (authoring sections, as appropriate)

Accountable for the accuracy of content created by the Medical Writer (specifically for IBs, summaries, CSRs, reports and other regulatory content)

Responsible for implementation of best practices and standards for Clinical Writing

Trains new Medical Writers for all aspects within a franchise

Provides critical feedback on templates as they relate to medical writing best practices and consistency

Notices trends and patterns in medical writing and initiates training program/communication/steps to improve input quality

For outsourced studies/deliverables, defines clinical outsourcing specifications and scope of work for clinical trial vendors. Oversees conduct of tasks.

Contributes to the development of clinical sections of regulatory documents like briefing packets, safety updates, regulatory submission documents, and responses to Health Authorities questions.

Writing and editing of pre-clinical and/or clinical reports.

Ensures timely development and completion of investigator brochure, clinical reports, summary documents, lay summaries, package inserts and other documents for submission to regulatory agencies.

Provides recommendations for the development of formats and guidelines for documentation.

What You'll Bring to Alcon:

Bachelor’s Degree or Equivalent years of directly related experience (or high school +13 yrs; Assoc.+9 yrs; M.S.+2 yrs; PhD+0 yrs) 

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

5 Years of Relevant Experience

How You Can Thrive at Alcon:

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!

Travel Requirements: 5-10%

Relocation assistance: Yes

Sponsorship available: No

Alcon Careers

See your impact at alcon.com/careers

#LI-DNI

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.

Find Jobs for Employees

Find Jobs for Contingent Worker

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 alcon.recruitment@alcon.com and let us know the nature of your request and your contact information.