At , 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 . As a Clinical Site Manager supporting the U.S. Clinical Development Team, (U.S. Remote-AZ, CA, CO, ID, NM, OR, UT, WA, NC) a typical day will include:

Site Selection and Initiation:

• Assist in the selection of investigative sites for clinical trials.

• Conduct site initiation visits to verify that site staff are properly trained and delegated to perform protocol assessments, are familiar with regulatory requirements, and understand proper handling and storage of ophthalmic drugs / devices.

• Ensure recruitment strategies are in place to meet enrollment targets.

• Confirm that site meets requirements to begin screening subjects.

Monitoring and Site Management:

• Conduct on-site and remote monitoring visits according to the protocol monitoring plan to ensure data quality and regulatory compliance.

• Review source documents, case report forms, and patient records.

• Verify the informed consent process is properly executed and adherence to the study protocol.

• Ensure that instruments / equipment used in the clinical trials are correctly calibrated, maintained, and utilized according to the study protocol and regulatory standards.

• Collaborate with Clinical Operations Lead and Clinical Trial Team (CTT) to identify and resolve site quality or study execution issues.

Regulatory Compliance:

• Ensure that the clinical trial sites are compliant with applicable regulatory requirements (e.g., FDA, ICH, GCP, ISO) regarding ophthalmic drugs / devices.

• Ensure that study sponsor and Investigator Site File is maintained and audit ready.

• Assists sites and CTT with internal and external audit / inspection-related activities including preparation, defining CAPAs, and ensuring CAPA targets are met.

Investigational Product (IP) and Clinical Supplies Oversight:

• Verify subject qualification and correct IP was dispensed / implanted.

• Ensure masking has been maintained, if applicable.

• Confirm full reconciliation of IP at the site level.

• Monitor drug / device-related safety and performance concerns and report them to the study sponsor.

• Ensure proper handling, storage, and accountability of investigational drugs and/or devices.

• Ensures appropriate clinical supplies are available, within expiry date and adequate for clinical trial.

• Data Management:

• Verify data accuracy and completeness, including instrument / equipment-generated data. Ensure data is securely stored.

• Collaborate with data management team to resolve data-related issues.

Safety Reporting:

• Ensure all safety issues are communicated and managed by the Principal Investigator according to regulatory and protocol requirements.

Close-Out Visits:

• Conduct close-out visits to ensure study documentation is complete, finalize data collection, and ensure all study-related activities are completed in accordance with the study protocol and regulatory requirements.

• Review Investigator obligations.

Documentation and Reporting:

• Complete comprehensive and accurate monitoring reports, including site follow-up letters.

• Ensure CTMS and eTMF are up to date and audit ready.

WHAT YOU’LL BRING TO ALCON:

• Bachelor’s Degree or equivalent years of directly related experience

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

• 2 Years of Relevant Experience

• 1 Years of Demonstrated Leadership

• Work hours: 40 hours

• Travel: 70%

• Company vehicle: Yes

• Relocation: No

• Sponsorship Assistance: No

Preferred Experience:

• Previous experience as a Clinical Research Associate, preferably in ophthalmology or a related therapeutic area.

• Knowledge of ophthalmic diseases, treatments, and related medical terminology, including ophthalmic devices.

• Strong understanding of clinical research regulations and Good Clinical Practice (GCP) guidelines.

• Excellent communication and interpersonal skills.

• Attention to detail and the ability to work independently and as part of a team.

• Willingness to travel as needed for on-site monitoring visits.

• Certification as a Certified Clinical Research Associate / Professional (CCRA / CCRP) or similar credential is a plus.

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 ’s mission to provide outstanding, innovative products and solutions to improve sight, improve lives, and grow your career!

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

Careers

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Total Rewards

’s Total Rewards programs are designed to align to incentives with business goals, encourage the right values and behaviors, and deliver long-term value. The first layer of our rewards program is compensation. We offer a combination of fixed pay and variable pay, which includes short-term incentives, and long-term incentives for eligible population. Our benefits program provides security for life events through life and disability insurance, supports savings for retirement, promotes good health and well-being and supports associates and their families during times of illness. To learn more about ’s Corporate Social Responsibility including our Total Rewards, <a rel="noopener noreferrer" href="https://nam12.safelinks.protection.outlook.com/?url=https%3A%2F%2Fs1.q4cdn.com%2F963204942%2Ffiles%2Fdoc_downloads%2F2021%2F09%2FAlcon_2020_Corporate_Responsibility_Report.pdf&data=04%7C01%7Cchris.lampley%40Alcon.com%7C8178fcaf5b784fd693c508d97e09bf79%7C34cd94b5d86c447f8d9b81b4ff94d329%7C0%7C0%7C637679402604440848%7CUnknown%7CTWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0%3D%7C1000&sdata=cetiSEzUutqrW%2FQE5c1b7WwVw2P6xxiAAsUsHnnt%2Fas%3D&reserved=0″>click here

Pay Range

$103,680.00 – $155,520.00

Pay Frequency

Annual

is an Equal Opportunity Employer and participates in E-Verify. 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. 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.