• Senior Clinical Research Auditor , GCP

    Job Location(s) US-TX-Dallas | US-FL-Daytona Beach | US-WI-Madison | US-Nationwide
    Job Number
    Job Category
    Quality Assurance
    Position Type
  • Job Overview

    Senior GCP QA Auditor

    Advance your career with a global leader


    Do you appreciate the importance of paying attention to details? Can you maintain flexibility in a changing environment?



    If you are looking to grow your career, you should consider joining Covance as a Senior GCP Quality Assurance (QA) Auditor. In this position, you will support Senior Management in maintaining robust quality systems while assuring regulatory compliance within Clinical Pharmacology (CPS) as you:


    • Audit clinical trials across multiple disciplines in compliance with appropriate SOPs, GCPs and all relevant industry regulations and guidance 
    • Perform external audits of investigator sites and service providers
    • Initiate and facilitate quality improvement objectives throughout the organization
    • Provide interpretation of external requirements and develop practical solutions to attain full compliance
    • Represent the company in direct interactions with client auditors and Health Authority inspectors
    • Collaborate with staff members of other functional groups to resolve issues
    • Mentor less experienced staff


    An office based candidate is highly preferred out of our offices in Dallas, TX; Madison, WI; or Daytona Beach, FL.


    Internal candidates may be considered in other US locations with home-based option.


    Working and growing at Covance



    At Covance, you’ll work in our energizing environment and support our client-centric solutions as one the world's largest and most comprehensive drug development services companies.



    You will receive a competitive compensation package with medical and dental insurance, tuition reimbursement, a 401(k) plan with a generous company match, along with short and long-term disability and life insurance.




    Why Senior QA Auditors choose to work at Covance


    • Join a global company for career development and growth opportunities
    • Identify unique solutions to make a direct impact in healthcare
    • Partner with and learn from compassionate colleagues and industry leaders



    Get to know Covance


    Beyond excellent compensation and benefits as a Senior QA Auditor, joining Covance opens the door to many career opportunities. Learn about what’s possible for your career when a company truly invests in you at



    Why Covance


    Bringing new medicines to market requires bold ideas. That’s why we empower our exceptional people with mentoring, in-depth training and tailored career planning. You’ll have the opportunity to own your career journey and develop alongside supportive, industry leaders who are passionate about your individual success. At Covance, you’ll discover your own extraordinary potential as you explore diverse projects and unique career paths across the drug development spectrum.



    Join us and discover your energized purpose as we transform possibilities into reality for our clients—and your career.


    Ready to join us? Let’s get started.





    • BA/BS four-year degree (science-related field desirable)



    A minimum of 5 years of experience working in the Pharma or CRO industries with at least 1 year of experience in clinical QA is required (GCP preferred). Experience in early phase clinical trials (Phase I – IIa) is highly desired and preferable. 


    Other essential requirements for this position include:

    • Demonstrated competencies in quality assurance practices and knowledge of regulatory compliance
    • Proficiency in Microsoft Office applications
    • Demonstrated negotiation skills with the ability to effectively provide constructive feedback and a proven track record of driving continuous improvement
    • Excellent communication and interpersonal skills with the ability to positively influence others



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