Designation: Drug Safety Associate/ Pharmacovigilance Department
Good understanding and experience of adverse event cases processing (ISCRs) from various sources such as Spontaneous, Post marketing surveillance Studies, Published Medical Literature, Health Authority/ Legal notification & Clinical Trials etc.
Experience 0.6 Months – 1 Year
M.Pharma/ B.Pharma/ BDS– Pharmacy
Please share your resume Rajavasudev.A@clinivigil.com