Auditor, RDQA Clinical Quality Audit - Remote
Cherry Hill, Camden County, New Jersey, 08034, USA
Listed on 2026-10-02
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Healthcare
Medical Science
About Abb Vie
Abb Vie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about Abb Vie, please visit us at Follow @abbvie on Linked In, Facebook, Instagram, X and You Tube.
Job DescriptionPrimarily responsible for the execution of the Clinical audit program, including scheduling, planning, reporting and resolution of Clinical audits. Ensuring alignment with RDQA policies and procedures wherever possible and contributing to the development and implementation of the Clinical QA quality system. Provision of advice and support on GCP and quality topics to business partners to ensure compliance with worldwide requirements and expectations.
Responsibilities:
- Assure quality and compliance in a regulated environment that includes worldwide regulations, country specific and other applicable standards and Abb Vie policies and procedures by continuous evaluation of Clinical processes through audit and QA oversight activities.
- Lead and participate in Clinical Audit scheduling, planning and conduct activities to assess compliance with regulations, guidelines, Abb Vie policies and procedures and sponsor requirements. Clinical audit types include investigator clinical site, process, system and Affiliate audits.
- Effectively communicate audit results, both orally and in writing, within target time frames.
- Review and approve Corrective Action Plans submitted in response to audit observations within target time frames and tracking of actions to completion.
- Advance the Abb Vie Quality System through contribution to the development and implementation of systems and processes required to support global quality assurance requirements. Supports maintenance or development of Quality standards relating to Clinical audit.
- Contribute to continuous improvement initiatives/projects to help assure compliance to regulations and corporate policies.
- Participate in and support GCP inspections, as required.
- Provide support and consultation to RDQA and business partners with regards to GCP regulations.
- Promote continuous education on quality and clinical guidelines and regulations for self and other Abb Vie staff.
- Bachelor’s degree in science (physical, life, health), a health care profession (e.g., nursing or pharmacy) or equivalent experience
- 3-5 years of experience in the biopharmaceutical industry or with a regulatory authority
- 3-5 years of experience in Quality Assurance and/or Clinical Research Development
- Strong analytical skills and the ability to draw conclusions from presented data
- Ability to work effectively and efficiently in a dynamic environment with minimal supervision
- High level of awareness and understanding of clinical trial regulations (e.g. ICH-GCP, EU Clinical Trial Directive/Regulation) and industry best practices
- Flexibility to adapt to changing assignments and ability to effectively prioritize
- Good project management, interpersonal, and communication skills with ability to work independently and as part of a team
- Willingness and ability to perform international travel
- Travel up to 40%
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state orlocal law:
- The compensation range described below is the range of possible base pay compensation that the Company believes ingood faith it will pay for this role at thetimeofthis posting based on the job grade for this position.
Individual compensation paid within this range will depend on many factors including geographic location,andwemayultimatelypaymore or less than the posted range. This range may bemodifiedin thefuture. - We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),medical/dental/vision insurance and 401(k) to eligible employees.
- This job is eligible toparticipatein our short-term incentive programs.
Note:
No amount of payis considered to bewages or compensation until such amount is earned, vested, and determinable.
Theamountandavailabilityof anybonus,commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employeeremainsin the Company'ssoleandabsolutediscretion unless and…
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