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Clinical Research & Clinical Data Management CDM

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Clinical Research & Clinical Data Management CDM

by BioMed Informatics Medwin Hospitals » Mon Oct 10, 2011 2:33 pm

Clinical Research, Pharma Research & Clinical Data Management -CDM
(ICH -GCP Guidelines, Pharmacovigilance & CDM + Project)

Medwin Hospitals, a Multi Speciality Hospital with excellence in modern health care ventures BioMed Informatics in the field of Clinical Research by keeping in view of the tremendous applications in improving the quality of the health care.

Clinical Research comprises of Pharma Research, Drug Development Process, 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.

OPPORTUNITIES:

According to Mc Kinsey Report, more than 50,000 Clinical Trials professionals are needed shortly in successful completion of USFDA/DCGI Investigational New Drug Applications (INDs).

The report by Ernst & Young states that globalization of Clinical Trials to newer options for the Indian clinical research industry. Excellent Opportunities are available in Abroad / India in this emerging field. In India alone, the clinical trials market of $ 35 million is expected to grow to nearly $ 300 million shortly.

Leading Organizations like Satyam Computers, Accenture, Cognizant Technology Solutions (CTS), i-GATE Technologies, Patni Computers, Tata Consultancy Services (TCS), Global Hospitals, NIMS, Gandhi Hospitals, Indo American Cancer Research Institute, Bharat Biotech, Biocon, Wockhardt, Reliance Life Sciences, Nicholas Piramal India, Asian Clinical Trials, Synchron Research Services Pvt Ltd, SIRO Clinpharm, Lotus Labs, Clingene, Aurobindo Pharma, Cipla, Ranbaxy,Vimta Labs, Dr.Reddy’s Lab…etc have been extensively involved in Clinical Trials. Many of MNCs like Pfizer, GlaxoSmithkline, AstraZeneca, Aventis, Novartis, Abbott Laboratories, inVentivSIRO,Merck….etc initiated CRO activities in India. International Contract Research Organizations like Allied Clinical Research, Bioclin Health Research, Clinimetrics, Covance, Eli Lilly, ICON Clinical Research, InfoQuest, Novum Pharmaceutical Research Services, Quintiles, Scirex, Synergos, Synteract, Trialstar, XenoTechalso initiated CRO operations in India providing excellent job opportunities.

Our candidates employed in Satyam Computers, ICMR, 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, AstraZeneca-UK, Texas Woman’s University-USA and many more…

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

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


Thanking you,

G.V.L.P. Subba Rao
Mobile: 09989684450
BioMed Informatics
Medwin Hospitals B Block First Floor,
Nampally, Hyderabad-500 001
Phone: 040 - 40209750 / 66821025
Website: http://www.biomedlifesciences.com
BioMed Informatics Medwin Hospitals
Registered User
 
Posts: 5
Joined: Thu Apr 14, 2011 10:50 am

Re: Clinical Research & Clinical Data Management CDM

by Mayur » Wed Apr 07, 2021 3:34 pm

Thanks for the information.
Mayur
Registered User
 
Posts: 1
Joined: Wed Apr 07, 2021 3:31 pm



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