Ann M.

An accomplished professional with over eight years of experience in the field of clinical research in Pharmaceuticals industry.
Broad Background of GCP, Pharmacovigilance and ICH guidelines including regulatory requirements.
Successfully managed FDA inspection conducted for the first time in BPO industry.
Proven track record of project management with the capacity to design, plan and implement ideas from conception through completion; able to manage multiple responsibilities without compromise to detail or quality.
Outstanding interpersonal skills; equally comfortable communicating one-on-one or addressing large audiences.
Proficient in Argus, Oracle, In Form, MS Office, Windows and Internet Applications.
Strong ability to translate technical information.
Exceptional in performing medical coding using Med DRA and WHO-Drug dictionaries and composes case narratives.