Pharmacovigilance, CDM, Medical Writing And SAS Programmer Jobs - PHARMA STUFF

Pharmacovigilance, CDM, Medical Writing and SAS programmer Jobs

ICBio as a Biometric Service provider, is expanding its wings as an International Clinical Research Service Provider.

Apply today for the below Positions

1) Clinical data management (CDM)

2) SAS Programmers minimum 5 Years Experience in CRO

3) PV & Medical Writers Experience of 3 to 5 years in CRO

All 3 roles play a crucial role in clinical trials and in the drug development process – from trial design to protocol development.

While CDM helps in generating rials: high-quality, reliable, and statistically sound data from giv clinical trials, statistics can help improve protocol development, data analysis and clinical trial reporting.

Pharmacovigilance represents all methods of detection, assessment, information and prevention of adverse drug reactions (ADRs)


DEADLINE IS: 22nd Jul 2021

image 8841a03c 2b8a 4156 b11a f45938940ab520210716 1338044611044889767269579 Pharmacovigilance, CDM, Medical Writing and SAS programmer Jobs

Leave a Comment

Scroll to Top