Clinical Research comprises of ICH-GCP Regulatory Affairs, Pharmacovigilance & Clinical Data Management-CDM for the effective management of clinical data related to the domains of investigational product and market available drug, Multicentrical data manipulation, tracking of Adverse events, Placebo, Active and Control Group Pharmacovigilance reports in accordance with 21 CFR USFDA Guidelines with Project.

You can be a part of Clinical Research as Clinical Research Associate, Clinical Research Coordinator, Principal Investigator, Co-investigator, Medical Writer, SOP Writer, Clinical Data Management Associate, Clinical Data Coordinator, Clinical Data Monitor, Clinical Data Auditor, Clinical Pharmacovigilance Associate, Regulatory Affairs Associate, Clinical Drug Safety Associate, Clinical CRF Designer, Clinical Data Design Analyst, Clinical Data Coder, Clinical Data Validator.

Our candidates employed in Satyam Computers, Global Hospitals, Apollo Hospitals, NIMS, Quintiles, Novartis, Glenmark Pharmaceuticals Ltd, Parexel International (India) Pvt Ltd, SMO Clinical Research (I) Pvt Ltd, Pioneer Corporate Services Inc-USA, Texas Woman’s University-USA and many more…

Interested candidates are kindly requested to fill the enquiry form in the website www.biomedlifesciences.com for further information.

Please note that we also provide separate hostel facility assistance for ladies as well as gents.

Thanking you,

Mr.Subba Rao

Mobile: 09989684450

BioMed Informatics

Medwin Hospitals B Block First Floor,

Nampally, Hyderabad-500 001

Phone: 040 - 40209750 / 66821025

Website: www.biomedlifesciences.com