Posted: 1 month ago

ICBio Clinical Research Pvt Ltd - Yelahanka

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+91 99011 11228
+91-2364 1033

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  • Specialized in: Medical & Health Care / Sales
  • Company name: ICBio Clinical Research Pvt Ltd
  • Locality: Yelahanka
  • Address: We have urgent requirement for Assistant Manager- Sales in CRO company,
    1)To identify potential new business contacts, market and coordinate with them for requirement of clinical trials.
    2) Designing the budget for the required clinical trial.
    3) Coordinating with the client for the payment and maintain the accounts for the same on project to project basis.
    4) Establish and maintain a computerized customer and prospect database.
    5) Identify and attend trade shows and other business functions to keep abreast of developments in the market place
    6) Managing the BDE team
    ICBio Clinical Research. Pvt. Ltd

    # 16, ICBio Tower, Chikkabetahalli,
    Yelahanka Main Road, Vidyaranyapura,
    Bangalore 5600971
Description for "ICBio Clinical Research Pvt Ltd - Yelahanka"

ICBio is a leading Contract Research Organization (CRO) based in Bangalore, INDIA, with a focus on offering End to End Research Services / Functional Service Providers (FSP) to the Global Pharmaceuticals, Biotech, Nutraceuticals, Herbals and Cosmetics Industries in India and the Emerging Markets across globe.

ICBio Clinical Research (ICBio CRO) specializes in conducting Clinical Research; Phase II - IV Clinical trials and Bioavailability / Bioequivalence studies (BA / BE studies) in Healthy volunteers as well as Patients, Bio-analytical, Safety & Pharmacovigilance

ICBio has a well-designed, State of art infrastructure to conduct various activities with independent operational areas for Clinical Trials, BA/BE studies, Medical Writing, Clinical Data Management and spread over a floor area of 20,000 sq.ft,

Our facility is approved by Drug Controller General of India (DCGI), ISO 9001:2012, ISO 15189:2012 / NABL Accredited Clinical Laboratory, Inspected and approved by Ministry of Health-Kazakhstan and other relevant regulatory authority requirements.

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