Pharmacovigilance (PV) is the science and activities relating to the detection, assessment, understanding and prevention of adverse effects or any other drug-related problem. The aims of PV are to enhance patient care and patient safety in relation to the use of medicines; and to support public health program by providing reliable, balanced information for the effective assessment of the risk-benefit profile of medicines.
An accurate and comprehensive Pharmacovigilence system throughout the clinical and post-marketing phases is essential for the protection of patients and public health. New directives and regulations that have been implemented to enhance patient safety monitoring can require significant additional resource, time and expertise.
Clinron solutions encompass the full product lifecycle, from initial clinical trials through post-market surveillance and risk management and minimization plans – including signal detection and trend analysis to identify and address safety across studies and integrated total safety management.
Clinron LLC offers competitive projects for eligible candidates in the field of Pharmacovigilence with varying positions like the Drug Safety Associate, Regulatory Affairs Specialist, Clinical Research Associate, Clinical Data Manager and Medical Writer. (hyperlinks)