Position: Regulatory Document QC Specialist
Location: Hybrid in Warren, NJ (3 days onsite / 2 days remote)
Duration: 3 months with potential extension
Pay Rate: $29/Hr - $33/HrJob Description: Our client is seeking a detail-oriented Regulatory Document QC Specialist to provide temporary support for approximately 3 months, with potential for extension. This is a junior-level role focused on ensuring the accuracy and consistency of scientific and regulatory documentation.
Responsibilities: Perform QC reviews of regulatory and scientific documents.
Cross-check data within regulatory documents against source documentation for accuracy and consistency.
Review document formatting, tables, references, and data presentation.
Identify and communicate discrepancies or required corrections.
Support general regulatory documentation and publishing activities as needed.
Qualifications Bachelor's degree in a scientific or related discipline preferred.
Strong attention to detail and ability to work with scientific/technical documents.
Regulatory or pharmaceutical/biotech experience preferred but not required.
Veeva experience is a plus.
Strong organizational and written communication skills.
Benefits:
This a contract position does not include employer-provided benefits.
Equal Opportunity Employer:
We are an Equal Opportunity Employer. All qualified applicants will receive consideration without regard to
race, colour, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.
Background Check:
Background checks may be conducted in accordance with applicable law.
Work Authorization:
Applicants must be authorized to work in the United States