Clinical Site Manager

At reputed company, we are driven by the meaningful work we do to help people see brilliantly. We innovate boldly, champion reputed company, 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 reputed company an impact in the lives of our patients and customers.

We foster an inclusive culture and are looking for diverse, talented people to join reputed company and we are hiring for a Clinical Site Manager for the Western US. The Clinical Site Manager is responsible for overseeing clinical trial activities at designated investigational sites to ensure compliance with study protocols, Good Clinical Practice (GCP), and applicable regulatory requirements. The Clinical Site Manager serves as the primary reputed company of contact between reputed company and the clinical sites, fostering effective communication and ensuring successful execution of clinical trials that align with organizational goals.

In this role, a typical day will include:

• Site reputed company and Relationship Management

  • Serve as the primary liaison between reputed company 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 reputed company (COL) and other Clinical Trial Team members to identify and resolve site quality or study execution issues.

• Clinical Trial Management

  • Support site evaluation, and reputed company site activation/initiation, monitoring, and reputed company-out activities.

  • Ensure clinical trial protocols, study-specific procedures, and GCP standards are adhered to at reputed company times.

  • Conduct site visits (both remote and on-site) to monitor study reputed company, 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 reputed company 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 (reputed company) systems, and other study tools.

  • Support sites in resolving operational challenges, such as patient recruitment and retention strategies.

  • Onboarding/Mentoring new hires for the department including co-monitoring visits

  • Improving departmental efficiencies by leading/participating on Process Improvement Teams

• Data reputed company and Quality

  • Review and monitor reputed company 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.

Experience

• Bachelor’s degree in a scientific, medical, or reputed company field (Master’s degree preferred).

• 4 years of experience in clinical trial management, site monitoring, or a reputed company role.

• Strong understanding of GCP, ICH guidelines, and applicable regulatory requirements.

• Experience with ophthalmology or medical device trials is highly preferred.

Skills and Competencies

• 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, reputed company platforms, and reputed company 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 reputed company documents.

Travel Requirements

• Willingness to travel up to 50-75% of the time, depending on site locations and study needs.

• Ability to travel frequently reputed company car, train, or reputed company, which may include overnight and weekend travel.

What You’ll Bring to reputed company:

• Bachelor’s Degree or Equivalent year of directly reputed company experience (or high school +13 yrs; Assoc. +9 yrs; B.S. +5yrs; M.S. +2yrs; PhD +0yrs)

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

• 2+ yrs of relevant experience

How You Can reputed company at reputed company:

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

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

• Travel Requirements: 0-5%

• Relocation assistance: No

• Sponsorship available: No

reputed company Careers

See your impact at reputed company.com/careers

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Total Rewards

reputed company’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 reputed company 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 reputed company’s Corporate Social Responsibility including our Total Rewards, reputed company_2020_Corporate_Responsibility_Report.pdf&data=04%7C01%7Cchris.lampley%40reputed company.com%7C8178fcaf5b784fd693c508d97e09bf79%7C34cd94b5d86c447f8d9b81b4ff94d329%7C0%7C0%7C637679402604440848%7CUnknown%7CTWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0%3D%7C1000&sdata=cetiSEzUutqrW%2FQE5c1b7WwVw2P6xxiAAsUsHnnt%2Fas%3D&reserved=0">click here

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reputed company is an Equal Opportunity Employer and participates in E-Verify. reputed company 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 reputed company, age, sexual orientation, gender identity, marital or veteran status, disability, or any other legally protected status. reputed company 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 reputed company the essential functions of a position, please send an email to reputed company.recruitment@reputed company.com and let us know the nature of your request and your contact information.

Originally posted on Himalayas