Job Reference: 115-21
Job Duration:
Start date: ASAP
Description:
Your main responsibilities will include the following;
Medical review of serious adverse events and non-serious adverse events from spontaneous reports and reports derived from regulatory authorities and the medical literature during postmarketing surveillance.
* Preparation and Medical review of Aggregate Reports (Periodic Safety Update Reports - PSURs, Periodic Adverse Drug Experience Reports - PADERs) required by global regulatory agencies for review of safety information for assigned products, when authorized to perform this function on behalf of a client.
* Reviewing laboratory values, adverse events, coding dictionaries and data tables, listings and figures as needed to identify drug safety issues in collaboration with the project physician
* Providing pharmacovigilance support toproject physicians, as appropriate
Industry: Pharmaceuticals
Salary:
Salary Benefits:
Vacancy Type: Permanent
Job Skills: Drug Safety, Pharmacovigilance, Physician, Doctor,Medical review, Senior Medical Director
Contact Name: Kiran Sahota
Website: -
Direct Application URL: -