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Online Resumes with "Drug Safety Associate"
Summary: Over 16 years of Drug Safety experience that includes Global Drug Safety project management in Clinical Research Organization and Sponsor (Pharmaceutical) environments. Experienced clinical trial and post-marketing studies. Participated in stand-alone and full service studies as Global Drug Safety/Pharmacovigilance Lead in addition to mentoring and managing a team of junior drug safety associates.
COVER LETTER: To whom it may concern: I am a Pharmacist with an equal combination of hospital and retail experience. I have seen many changes in healthcare over the past fifteen years of practice as well as the many pitfalls of a currently flailing economy. The aforementioned dynamics have affected the efficiency and safety of pharmacy. Of my prominent abilities are adapting to differing work environments and the staffing c...
To obtain a position as a Drug Safety Associate.
Tags for this Online Resume: Distribution, Training, Data General Nova, Chemistry, High Performance Liquid Chromatography (HPLC), PEDIATRIC, Inventory, Inventory Control, Cancer, Chemotherapy, oncology, clinical, pharmaceutical, gcp, ich, protocol, phase, sas
SUMMARY OF QUALIFICATIONS More than 9 years' experience as licensed pharmacist in Maryland the fields of Retail Pharmacy (chain, independent and LTC), Hospital (outpatient and inpatient). More than 5 years in Government (State Medicaid and Federal) settings, as well as Drug Safety Associate.
Interested in a drug safety associate position in biotechnology/pharmaceutical industry.
SUMMARY * Pharmacovigilance Associate with over 2+ years of experience in Drug Safety and Clinical practice fields with clear understanding of EDC (Electronic Data Capture) * Experience in performing successful data management, triage, case entry, MedDRA, WHOdrug dictionaries, narrative writing, peer review, case follow-up, case review and report preparation * Performing Data entry and Quality check adverse event reports fr...
I would like to begin a career in drug safety/pharmacovigilance.
I have extensive experience in writing clinical and regulatory documents in the Pharmaceutical industry which include regulatory and safety I have completed medical encoding (MeDRA), data and quality review management. My past experience included responsibilities for preparing safety sections within key documents such as Investigations Brochure, clinical study reports, writing safety narratives to be included in final stud...