PVG QC Reviewer II - Contract - Plainsboro, NJ
Proclinical is seeking a dedicated Pharmacovigilance QC Reviewer II for a hybrid role focused on ensuring the quality and compliance of pharmacovigilance case handling.
Primary Responsibilities:
The successful candidate will play a pivotal role in ensuring the highest standards are upheld in the submission of Individual Case Safety Reports (ICSRs) within the diabetes therapy area.
Skills & Requirements:
- Bachelor's degree required; healthcare professional degree preferred (e.g., pharmacist or nurse).
- Strong analytical skills with experience in pharmacovigilance case processing.
- Proficiency in using safety databases and MS Office applications (Outlook, Excel, Word).
- Excellent written and verbal communication skills.
The PVG QC Reviewer II's responsibilities will be:
- Handle pharmacovigilance cases from intake to submission of ICSRs.
- Conduct thorough quality control of ICSRs to ensure adherence to internal and external health authority regulations, including 21 CFR FDA PostMarketing.
- Work with safety databases, such as Argus, to manage case data effectively.
- Identify nonconformances and communicate feedback or escalate issues as necessary.
Compensation:
If you are having difficulty in applying or if you have any questions, please contact Shannon Briggs at s.briggs@proclinical.com
If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.
Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy.
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