Hiring.Camp

Manager, Quality Assurance

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·

Yesterday

Location
US, Blue Bell (ICON), United States of America
Workplace
Remote
Type
Full-time
Department
IT
Seniority
Manager
Experience
5+ years
Education
Bachelor
Visa
Not sponsored
Source
Workday

Description

Manager, Quality Assurance

At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.


As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.


As a Process, Training and Execution Lead at ICON, you will ensure the quality and compliance of clinical trials, interpreting regulatory requirements, and contribute to the advancement of innovative treatments and therapies.


What You Will Do:

Your focus will be on coordinating quality assurance and compliance delivery, resolving issues, and developing team capability.

Key responsibilities include:

  • Developing and implementing quality assurance strategies and processes to support clinical trial activities.
  • Conducting quality assessments and audits to ensure compliance with regulatory standards and guidelines.
  • Collaborating with project teams to identify and address quality issues and implement corrective actions as needed.
  • Providing guidance and support to staff regarding quality assurance policies, procedures, and best practices.
  • Contributing to the development and maintenance of quality management systems and documentation.

Your Profile:

You will have solid quality assurance and compliance experience, with the ability to manage competing priorities and develop your team.

Required qualifications and experience:

  • Bachelor's degree in a relevant discipline
  • Minimum of 5 years of experience in quality assurance within the pharmaceutical, biotechnology, or CRO industry.
  • Knowledge of regulatory requirements and guidelines governing clinical trials (e.g., ICH-GCP, FDA regulations).
  • Strong analytical and problem-solving skills, with the ability to identify and resolve quality issues effectively.
  • Excellent communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams and stakeholders.
  • Willingness to travel as required (approximately 35%)

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.


Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.


Benefits may include:

  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.


Visit our careers site to read more about the benefits ICON offers.


Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.


If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.


Are you a current ICON Employee? Please click here to apply

Skills

GCPClinical TrialsFDACompliance

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