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CRO

  • Require Study Start Up Associate at ICON

    ICON is a global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. We specialize in the strategic development, management and analysis of programs that support Clinical Development – from compound selection to Phase I - IV clinical studies ICON enjoys a strong reputation for quality and is focused on staff development.

    Post : Study Start Up Associate I

  • Work as Synthesis Chemist / Associate at Chemveda Life Sciences | 20 posts

    Chemveda Life Sciences is a rapid-growing contract research organization based out of Hyderabad, providing customized services to global partners across the pharmaceutical, biotechnology, and agro industry. Founded in the year 2008, Chemveda has made significant investments in terms of building a strong scientific team, able infrastructure and client specific business models, enabling us to provide quality R&D services across the drug discovery and development value chain.

    Post : Synthesis Chemist / Associate (CRO)

  • Job for Clinical Research Coordinator at Nomad Life Sciences Pvt Ltd

    Nomad Life Sciences Pvt Ltd is a Clinical Trial Management Organization with extended clinical research capabilities having a distinguished investigator network throughout India. We offer effective clinical trial management services with solutions to the Pharmaceutical and Biotechnology companies.

    Post : Clinical Research Coordinator - 02 posts

  • Job for Clinical Research Associate at PRA Health Sciences

    PRA Health Sciences, providing innovative solutions for our clients is what we do. Side-by-side with our clients, we strive to move drug discovery forward, helping them to develop life-saving and life-improving drugs. With our unique blend of expertise, we provide comprehensive clinical development services across all phases. From full service clinical development to the pioneering Embedded SolutionsTM model, PRA provides a broad spectrum of solutions that meet the demands of a diverse marketplace.

    Post : Clinical Research Associate

  • Work as Clinical System Tester at PRA Health Sciences

    PRA Health Sciences, providing innovative solutions for our clients is what we do. Side-by-side with our clients, we strive to move drug discovery forward, helping them to develop life-saving and life-improving drugs. With our unique blend of expertise, we provide comprehensive clinical development services across all phases. From full service clinical development to the pioneering Embedded SolutionsTM model, PRA provides a broad spectrum of solutions that meet the demands of a diverse marketplace.

    Post : Clinical System Tester

  • Job for Clinical Process Associate at QREC Clinical Research LLP

    QREC is an CRO based at Hyderabad and Jaipur offering services to the healthcare Industry from past 8 years in field of Medical Sciences research.

    Post : Clinical Process Associate

  • Vacancy for Medical Writer at QREC Clinical Research LLP

    QREC is an CRO based at Hyderabad and Jaipur offering services to the healthcare Industry from past 8 years in field of Medical Sciences research.

    Post : Medical Writer

  • Opportunity as Head in Analytical Research & Development at Syngene International

    Syngene International is one of India’s premier contract research and manufacturing organizations in providing customized service. Our services encompasses all across discovery chain: early stage discovery, process development, cGMP manufacturing and formulation development both in the small molecule and novel biologics area. Based in Bangalore, Karnataka, the Company is situated in a 90 acre Special Economic Zone with over 100000 sq. mt of built up facilities. The state-of-the-art research facilities have been qualified by various pharmaceutical majors & regulatory agencies and has received various certifications including ISO 9001: 2008, ISO 14001:2004, OHSAS 18001:2007, GLP and AAALAC.

    Post : Head - Analytical Research & Development

  • Career for Clinical Research Associate at Medpace

    Medpace is a scientifically-driven, global, full-service clinical contract research organization (CRO) providing Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Medpace’s mission is to accelerate the global development of safe and effective medical therapeutics through its high-science and disciplined operating approach. We leverage local regulatory and deep therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, Medpace employs approximately 2,500 people across 35 countries

    Post : Clinical Research Associate

  • Require Regulatory Submissions Coordinator at Medpace

    Medpace is a scientifically-driven, global, full-service clinical contract research organization (CRO) providing Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Medpace’s mission is to accelerate the global development of safe and effective medical therapeutics through its high-science and disciplined operating approach. We leverage local regulatory and deep therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, Medpace employs approximately 2,500 people across 35 countries.

    Post : Regulatory Submissions Coordinator

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