Covance Senior Clinical Research Auditor , GCP in Chantilly, Virginia
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 willsupport 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 http://careers.covance.com/possibilities.html
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
Job Number 2018-20037
Job Category Quality Assurance
Position Type Full-Time
Covance is committed to diversity in the workplace and is an equal opportunity employer (Minority/Female/Individual with Disability/Veteran/Sexual Orientation/Gender Identity). Your confidentiality and privacy are important to us.