Pharmacovigilence Drug Safety PVG Scientists
Thursday, August 24, 2006
Clinical Pharmacovigilence Drug Safety PVG Scientists / clinicians to join a world-renowned organisation in clinical research / clinical trials projects. Do you have the organisational skills and qualifications to ensure your drug safety standards are being performed on a regular basis to avoid punitive measures being taken? Can you run an efficient compliant safety department? Be involved in the maintenance of standard operating procedures and working practice directives (SOPs and WPDs) in addition to ICH / local guidelines relating to clinical trials. Develop a strong understanding of safety requirements and prepare for pharmacovigilance inspections conducted by regulatory agencies. As a PVG Scientist / Pharmacovigilance manager or assistant, you will be responsible for the overall co-ordination of serious adverse event (SAE) processes, database / data management activities and the accurate collection of data relating to patient safety is essential. You should know ICH-GCP regulatory requirements and practice and depending upon your level of expertise and experience in nursing / healthcare or pharamcovigilence to be offered either a senior position or trainee assistant post. Team Managers are responsible for scientists clinical associates and administration staff. In return for your commitment to precision, attention to detail, excellent communication abilities, you will be offered exceptional long-term career prospects, training and attractive benefits.
Call Nicola Worthington on +44 (0)1628 418151 or email firstname.lastname@example.org