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)

SEND YOUR CV TODAY
hrd@icbiocro.com

DEADLINE IS: 22nd Jul 2021