Quality Control Specialist will provide support to the Regulatory Affairs for QC of Medical Writing and other documents as needed. Responsibilities will include QC of all documents written in Medical Writing to include protocols, protocol amendments, investigator brochures, clinical study reports, and regulatory documentation. The QC Specialist is responsible for performing accurate, precise proof- reading to include spelling, grammar, punctuation and verification of data.
Masters degree in English/Life Sciences. 2 years experience in pharmaceutical industry. Proficient in Microsoft Office, Documentum, Hyperlinking and Bookmarking.
Candidate must come onsite to NJ for Orientation, Interview and 1st week of project.
Company offers very competitive hourly rate for contract role and great working environment.