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Kindly reply me back for this particular requirement ASAP. if you do have any matching resume regarding this requirement. I will be highly obliged with your co-operation. if you do want to have any discussion you can call us at 412-499-3197. Please feel free to call us. Waiting for your reply ROLE: QC Specialist - Regulatory Affairs (Quality Control Specialist) Duration: 6 - 12 + Months LOCATION: Ridgefield park NJ Client : Direct Description of Services Required: 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 â€"reading to include spelling, grammar, punctuation and verification of data. Must have a working knowledge of AMA style guide, submissions and FDA QC guidelines. Hyperlinkling and bookmarking experience is required Qualifications: MUST HAVE: Masters degree in English/life Sciences. 2 years experience in pharmaceutical industry. Proficient in Microsoft Word, Excel, and Documentum. *Thanks,* ** *Puneet Tandon* *Sourcing Specialist* iBusiness Solution LLC (Certified 8(a), MBE, WBE Business in PA, MD,VA & NJ) 1121 Boyce Road, Suite 2100 A Pittsburgh, PA 15241 Phone: 412-499-3197 Fax: 412-202-8931 Email: [EMAIL PROTECTED] <[EMAIL PROTECTED]>* Visit us at www.ibusinesssolution.com --~--~---------~--~----~------------~-------~--~----~ You received this message because you are subscribed to the Google Groups "DIRECT CLIENT IT NEED" group. To post to this group, send email to [email protected] To unsubscribe from this group, send email to [EMAIL PROTECTED] For more options, visit this group at http://groups.google.com/group/direct-client-it-need?hl=en -~----------~----~----~----~------~----~------~--~---
