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  • 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

  • Work as Sr. Manager/ AGM in Business Development at Panacea Biotec | Ph.D, B.Pharm, M.Sc, MBA

    Panacea Biotec is a leading research based Health Management Company, with an annual turnover of approx. Rs. 830 Crores. We are engaged in research, development, manufacture & marketing of Vaccines, Bio-Pharmaceuticals and Pharmaceuticals (Rx & OTC) of international quality and Health Services. All Panacea Biotec plants are accredited by international agencies and they follow current Good Manufacturing Practices, as per WHO guidelines.

    Post : Sr. Manager/ AGM – Business Development – Contract Research(CRO)

  • Job for M.Pharm, M.Sc in R&D at Piramal Enterprises

    Piramal Enterprises Limited is the flagship company of the Piramal Group.  Starting from the mid-1980s, PEL has shifted its focus from the textiles industry, and established its entrepreneurial credentials in Pharma, Information Management, and Financial Services. It has grown organically and inorganically and often made contrarian business calls.  When Indian pharmaceutical industry was focused on international generics, we invested in domestic formulation businesses.

    Post : Sr. Research Associate/ Research Scientist

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  • Job for Research Associate at Syngene International | M.Pharm, M.Sc

    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 : Research Associate

  • Career for Clinical Research Associate at PRA International

    A leading global CRO, PRA is transforming clinical trials through our people, innovation and transparency. We serve clients across all phases of pharmaceutical and biotech drug development by combining therapeutic and operational expertise with local knowledge PRA’s commitment to excellent in research begins with our people.  Our workforce has grown by over 25% since 2010 and now comprises over 4,700 employees spanning more than 13 time zones and speaking more than 15 languages. It is our philosophy that the way in which we grow our business is to focus on our employees and as such, we recognize that successful careers are found within organisations that provide the support that employees need at work, as well as the benefits they require outside the office.

    Post : Clinical Research Associate

  • Job as Trainee / Internship(30 posts) at Clinwave Research - CRO

    Clinwave Research (CW-India)  is a Contract Research Organization (CRO), head quartered in the heart of India's healthcare services and IT hub, Hyderabad. Since then CW-India has been providing exceptional site management and project management and monitoring of phase II, III and IV clinical trials involving pharmaceutical products to its Clients/Sponsors. We maintain High retention of our clients due to our commitment, responsiveness, flexibility, performance, cost effectiveness and unmatched quality. We complement each client's working culture and management style and are flexible to their requirements.

    Post : Industrial Training /  Trainee / Internship

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