Manager, Good Clinical Practices

Alcon

$110K — $143K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's Degree or Equivalent experience
  • Fluency in English (reading, writing, communicating)
  • 5+ Years of Relevant Experience
  • Experience with GCP regulatory requirements
  • Willingness to travel domestically and internationally (up to 60%)

Responsibilities

  • Lead compliance activities to meet GCP standards
  • Manage individual projects for operational efficiency
  • Oversee daily operations to ensure departmental alignment
  • Implement quality management systems throughout processes
  • Conduct and support inspections and audits for compliance
  • Manage internal and external audits, ensuring site preparedness
  • Report and address quality issues and recommend corrective actions

Benefits

  • Health and life insurance
  • Retirement plans
  • Flexible time off
  • Opportunities for career growth and development
  • Robust benefits package supporting associates and families
Full Job Description
This role is part of Alcon's Quality & Regulatory Affairs function, a team that ensures our products are in compliance with global, local, and internal regulations and meet the strictest standards of quality as we help people see brilliantly.

The Manager, Good Clinical Practices (GCP) is primarily responsible for leading compliance activities, providing technical expertise, and driving quality improvement projects. You will manage external audits, ensure site preparedness, and coordinate Corrective and Preventive Action (CAPA) processes.

As a Manager, Good Clinical Practices supporting the QA Compliance Team in Fort Worth, TX, Durham, NC, Johns Creek, GA, or Lake Forest, CA, a typical day will include:

  • Manage individual projects, applying advanced knowledge to achieve objectives and impact project performance and operational efficiency.
  • Oversee day-to-day operations, ensuring productivity and alignment with departmental objectives.
  • Make operational decisions, managing programs, resources, and schedules.
  • Ensure implementation of quality management systems at every stage of process/operations.
  • Implement quality assurance regulations and write, revise, review and approve standard operating procedures.
  • Perform and support inspections/audits of processes and documents associated with studies/facilities/ equipment/suppliers/vendors to ensure that activities comply with applicable GCP/GLP regulatory requirements, standard operating procedures, and study protocols.
  • Manage, support, and facilitate internal and external audits/regulatory inspections, ensure site preparedness, and coordinate Corrective and Preventive Action (CAPA) processes.
  • Report potential issues with quality, compliance, ineffective processes/procedures, and deviations and recommend appropriate corrective & preventive actions.
  • Lead implementation of new regulations, regulatory guidance, and international standards.
  • Ensure adherence to Good Practice (GxP) regulations by following Standard Operating Procedures (SOPs), maintaining accurate documentation, ensuring rigorous quality, and completing required training.
  • Commitment to continuous improvement and compliance with regulatory requirements.


All associates must adhere to GxP regulations by strictly following Standard Operating Procedures (SOPs), maintaining accurate and complete documentation, ensuring rigorous quality control, and completing all required training. Associates are responsible for meeting their individual job requirements and contributing to the overall compliance of the organization. Compliance with regulatory requirements and a commitment to continuous improvement are essential to our operations.

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
  • Work Location: Onsite
  • Travel: Domestic and International - as required up to 60%
  • Relocation: No
  • Sponsorship Assistance: No


PREFERRED QUALIFICATIONS/SKILLS/EXPERIENCE:
  • Knowledge of ISO 14155, ICH E6, Medical Device EU, FDA regulatory requirements, and Declaration of Helsinki
  • Validated GCP audit track record
  • Good analytical skills and judgment
  • Advocate for outstanding quality and compliance standards - does not compromise on customer expectations and regulatory requirements


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 a 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.

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Compensation and Benefits

Alcon's Total Rewards programs are designed to align incentives with business objectives, support our values, and deliver long-term value. Our compensation approach includes a combination of fixed and variable pay, with short-term and long-term incentive opportunities for eligible roles. Our benefits offerings are designed to support associates and their families across key life events, including programs that promote health and well-being, provide financial security, and support retirement planning.

The salary range posted represents the anticipated hiring range for this role. Actual compensation may vary based on factors such as experience, skills, location, and internal equity, and may fall outside the posted range.

Pay Range
110,500.00 - 143,000.00

Pay Frequency
Annual

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