Title: Quality Control (QC) Consultant Location: Edison, NJ
Length: 1 Year+ *Need consultants who have worked for Pharma and specifically in Clinical Trials* Responsibilities and requirements for QC Consultant Candidates should have worked with direct GCP Document QC (Protocols, Investigator Brochures, Clinical Study Reports) and/or QA experience 1. Ability to conduct an independent QC review on a variety of GCP related study documents (eg, CSRs, protocols, and IB updates) according to Daiichi Sankyo processes and Health Authority requirements/conventions, and document the QC results 2. Ability to provide input into QC plans and processes relating to Trial Master File management; 3. Ability to adapt easily to new circumstances and be flexible in a work environment that makes frequent changes in its demands; 4. Project management skills and the ability to work as part of a team; 5. Ability to influence and maintain open and frequent communications with external and internal (DS) stakeholders; 6. Solid GCP knowledge and understanding of clinical trials 7. Strong working knowledge of Microsoft Office Suite (PowerPoint, Excel); 8. Light administrative tasks including meeting planning & scheduling Thanks & Regards, Ramesh Kumar *Global **Associates Inc/ **VCarve Inc* *||* 7106 Corporate Way* ||* Dayton, OH 45459 *||* *||*Phone: 937-877-5870 * ||* Fax: 937-312-1205 *||* ram...@gassociates.com* or* ram...@vcarve.com *||* www.gassociates.com*||* <http://www.gassociates.com||/> -- You received this message because you are subscribed to the Google Groups "REQSRESUMES" group. To unsubscribe from this group and stop receiving emails from it, send an email to reqsresumes+unsubscr...@googlegroups.com. To post to this group, send email to email@example.com. Visit this group at http://groups.google.com/group/reqsresumes. For more options, visit https://groups.google.com/d/optout.