Remote opportunity at
AbbVieAuditor, RDQA Clinical Quality Audit - Remote
AbbVie is a healthcare company focused on creating innovative medicines and solutions for complex medical challenges across therapeutic areas like oncology, immunology, neuroscience, and aesthetics. The…
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About This Role
AbbVie is a healthcare company focused on creating innovative medicines and solutions for complex medical challenges across therapeutic areas like oncology, immunology, neuroscience, and aesthetics. The organization is currently hiring a remote Auditor, RDQA Clinical Quality Audit on a full-time basis to execute clinical audit programs and uphold regulatory standards. This position centers on carrying out audit scheduling, planning, reporting, and issue resolution aligned with Research and Development Quality Assurance…
Job Description
AbbVie is a healthcare company focused on creating innovative medicines and solutions for complex medical challenges across therapeutic areas like oncology, immunology, neuroscience, and aesthetics. The organization is currently hiring a remote Auditor, RDQA Clinical Quality Audit on a full-time basis to execute clinical audit programs and uphold regulatory standards.
This position centers on carrying out audit scheduling, planning, reporting, and issue resolution aligned with Research and Development Quality Assurance policies. The ideal candidate will provide guidance on Good Clinical Practice standards to business partners, review corrective action plans, and support health authority inspections. This role suits professionals experienced in quality assurance or clinical research who can navigate dynamic environments independently and adapt to shifting priorities.
Eligible employees receive a total rewards package that includes medical, dental, and vision insurance, paid time off for holidays, sick leave, and vacations, a 401(k) plan, and participation in short-term incentive programs.
Responsibilities
- Manage the clinical audit program through scheduling, planning, reporting, and resolution activities
- Evaluate clinical processes via audits and quality assurance oversight to ensure compliance with global regulations and company policies
- Conduct various types of clinical audits, including investigator sites, processes, systems, and affiliates
- Communicate audit findings orally and in writing within established deadlines
- Review and approve corrective action plans and track resolved actions to completion
- Contribute to the enhancement of the quality system and global quality assurance requirements
- Participate in GCP inspections and support consultations for business partners
- Promote continuous education regarding quality guidelines and clinical regulations
Requirements
- Possess 3 to 5 years of experience within the biopharmaceutical industry or working for a regulatory authority
- Bring 3 to 5 years of professional background in Quality Assurance or Clinical Research Development
- Demonstrate a strong understanding of clinical trial regulations such as ICH-GCP and the EU Clinical Trial Directive or Regulation
- Willingness and ability to undertake international travel
Qualifications
- Hold a Bachelor’s degree in a physical, life, or health science, a healthcare profession like nursing or pharmacy, or equivalent experience
Core Skills
Benefits
- Paid time off covering vacation, holidays, and sick leave
- Medical, dental, and vision insurance coverage
- Participation in a 401(k) retirement plan
- Eligibility for short-term incentive programs
Frequently Asked Questions
Answers are based only on the employer’s listing; where it doesn’t say, neither do we.
Is this position remote?
Yes, this is a remote job posting.
What is the employment type?
This is a full-time position.
What salary does this role offer?
The source posting does not specify the salary for this role.
What travel is required for this role?
The position requires a willingness and ability to perform international travel.
Sample Interview Questions
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