What are the responsibilities and job description for the Sr. Manager, Clinical Site Operations position at Alcon?
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. Manager Clinical Site Operations supporting the U.S. Clinical Development Team, a typical day will include:
Key Responsibilities:
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.
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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.
We foster an inclusive culture and are looking for diverse, talented people to join Alcon. As a Sr. Manager Clinical Site Operations supporting the U.S. Clinical Development Team, a typical day will include:
Key Responsibilities:
- Team Leadership and Management:
- Recruit, train, mentor, and manage a team of associates and contractors within assigned region.
- Manage associate performance through workload balance and coaching by providing ongoing feedback and development opportunities.
- Foster a collaborative and supportive team environment.
- Operational Oversight:
- Oversee the execution and monitoring of clinical trials within the assigned region.
- Ensure that all clinical research activities are conducted in compliance with protocols, regulatory requirements, and company standard operating procedures (SOPs).
- Supports recruitment strategies in place to meet patient enrollment targets for their region.
- Provides oversight and supports site initiation, patient recruitment, data collection, and site close-out activities.
- Quality and Compliance:
- Ensure adherence to Good Clinical Practice (GCP) guidelines and other applicable regulations.
- Conduct observational site visits to ensure data integrity and compliance with study protocols.
- Address and resolve any issues or deviations promptly.
- Oversee activities related to internal and external audits/inspections in their region including preparation, defining CAPAs, and ensuring all CAPA targets are met.
- Stakeholder Collaboration:
- Collaborate with cross-functional teams, including trial management operations, clinical quality assurance, data operations, and regulatory affairs.
- Participate in clinical trial meetings and provide updates on site activities, as needed.
- Resource Management:
- Collaborate with other Regional Managers to balance workload.
- Ensure efficient allocation of CRAs to clinical sites based on study needs and priorities.
- Continuous Improvement:
- Identify opportunities for process improvements and implement best practices to enhance the efficiency and quality of clinical trials.
- Stay current with industry trends, regulatory changes, and advancements in clinical research methodologies.
- 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
- 5 Years of Demonstrated Leadership
- Work hours: 40
- Travel: 20-25%
- Relocation: no
- Sponsorship Assistance: no
- 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.
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 Employees
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.