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 Sr. Associate, Clinical Site Manager supporting the U.S. Clinical Development Team, in Remote TX, AL, AR, LA, MS, OK, a typical day will include:
Key Responsibilities
Site Oversight and Relationship Management
Serve as the primary liaison between Alcon and assigned clinical sites.
Build and maintain strong relationships with site staff, investigators, and key stakeholders.
Facilitate effective communication and address site-specific concerns or challenges promptly.
Actively engages with the Clinical Operations Lead (COL) and other Clinical Trial Team members to identify and resolve site quality or study execution issues.
Clinical Trial Management
Support site evaluation, and oversee site activation/initiation, monitoring, and close-out activities.
Ensure clinical trial protocols, study-specific procedures, and GCP standards are adhered to at all times.
Conduct site visits (both remote and on-site) to monitor study progress, identify issues, and ensure timely data collection in accordance with the study-specific monitoring plan and relevant SOPs/Job Aids.
Regulatory and Compliance Support
Ensure sites comply with regulatory requirements, including IRB/IEC submissions and approvals.
Assist in resolving compliance issues and ensure corrective and preventive actions are implemented effectively.
Training and Support
Provide ongoing training and guidance to site staff regarding protocol requirements, electronic data capture (EDC) systems, and other study tools.
Support sites in resolving operational challenges, such as patient recruitment and retention strategies.
Data Integrity and Quality
Review and monitor source documents and case report forms to ensure data accuracy and completeness.
Work with the data management team to resolve queries and discrepancies in a timely manner
WHAT YOU’LL 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: 40 hours
Travel: 50-75%
Relocation: No
Sponsorship Assistance: No
Preferred Experience:
Strong understanding of GCP, ICH guidelines, and applicable regulatory requirements.
Experience with ophthalmology or medical device trials is highly preferred.
Excellent interpersonal and communication skills to build and maintain site relationships.
Strong organizational and multitasking abilities to manage multiple sites and studies simultaneously.
Analytical and problem-solving skills to identify and address issues proactively.
Proficiency in clinical trial management systems (CTMS), eTMF, EDC platforms, and Microsoft Office Suite.
Ability to work independently and collaboratively in a fast-paced environment.
Physical Demands
Ability to sit, stand, and walk for extended periods of time during site visits and monitoring activities.
Must have the ability to lift and carry up to 25 pounds (e.g., clinical materials, equipment).
Prolonged periods of working on a computer and reviewing electronic and paper documents.
Ability to travel frequently via car, train, or air, which may include overnight and weekend travel.
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.
Find Jobs for Contingent Worker
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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