Skip to main content
  • Multiple vacancies for posts of Clinical Data Analyst, Drug Safety Associate, Associate Medical Writer, Senior Associate - Regulatory Affairs in Parexel

    PAREXEL has supported the Bio-Tech and Pharmaceutical industries in helping the development of new drugs and treatments on a global basis. As a leading global biopharmaceutical service provider, they supply knowledge-based contract research, medical communications and consulting services across a broad range of therapeutic areas to the worldwide pharmaceutical, biotechnology and medical device industries.

  • Opening for Pharmacovigilance Data Manager in Novartis
    Opening for Pharmacovigilance Data Manager in Novartis

    A global healthcare leader, Novartis has one of the most exciting product pipelines in the industry today. A pipeline of innovative medicines brought to life by diverse, talented and performance driven people. All of which makes them one of the most rewarding employers in their field.

    Post: Pharmacovigilance Data Manager

  • Required for Drug Safety Associate / Senior Drug Safety Associate in Icon Clinical Research - degree in pharmacy, science
    Required for Drug Safety Associate / Senior Drug Safety Associate in Icon Clinical Research - degree in pharmacy, science

    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. We make it our mission to attract the most diverse and creative minds into the business and we continually strive to provide opportunities for our people to excel, grow and build a great career. We understand that our greatest asset is the skills and talents of our people and they are truly what set us apart.

    Post: Drug Safety Associate / Senior Drug Safety Associate - 008559

  • Career to work as Strategic Resourcing, Quality Lead / Coordinator @ inVentiv Health Clinical
    Career to work as Strategic Resourcing, Quality Lead / Coordinator @ inVentiv Health Clinical

    inVentiv Health Clinical, a leader in drug development services, has a global infrastructure, therapeutic expertise, and commitment to quality that is unmatched in the industry. For pharmaceutical, biotechnology, generic drug, and medical device companies of all sizes around the world, inVentiv Health Clinical can help you transform promising ideas into commercial reality.

    Post: Strategic Resourcing, Quality Lead / Coordinator

  • Career opportunity for Clinical Team Manager (Based in any APAC) in PPD Pharmaceuticals
    Career opportunity for Clinical Team Manager (Based in any APAC) in PPD Pharmaceuticals

    PPD is a leading global contract research organization providing discovery, development and post-approval services as well as compound partnering programs. Our clients and partners include pharmaceutical, biotechnology, medical device, academic and government organizations. With offices in 32 countries and more than 9,000 professionals worldwide, PPD applies innovative technologies, therapeutic expertise and a commitment to quality to help its clients and partners maximize returns on their R&D investments and accelerate the delivery of safe and effective therapeutics to patients

    Post: Clinical Team Manager (Based in any APAC)-114961

  • Apply Online for the post of Clinical Project Manager in Quintiles
    Apply Online for the post of Clinical Project Manager in Quintiles

    Quintiles is the only fully integrated biopharmaceutical services company offering clinical, commercial, consulting and capital solutions worldwide. Our network of 23,000 engaged professionals in 60 countries around the globe works with an unwavering commitment to patients, safety and ethics — ensuring a higher level of healthcare for people. For our biopharmaceutical customers, we help them navigate risk and seize opportunities in an environment where change is constant.

    Post: Clinical Project Manager-1307044

  • Opportunity to work as Compliance Specialist in Icon Clinical Research
    Opportunity to work as Compliance Specialist in Icon Clinical Research

    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. We make it our mission to attract the most diverse and creative minds into the business and we continually strive to provide opportunities for our people to excel, grow and build a great career. We understand that our greatest asset is the skills and talents of our people and they are truly what set us apart.

    Post: Compliance Specialist - 008156

  • Advanced Centre for Treatment, Research and Education in Cancer recruiting Clinical Trial Coordinator | Walk in interview
    Advanced Centre for Treatment, Research and Education in Cancer recruiting Clinical Trial Coordinator | Walk in interview

    The Advanced Centre for Treatment, Research and Education in Cancer (ACTREC, Kharghar, Navi Mumbai is the new state-of-the-art R&D satellite of the Tata Memorial Centre (TMC), which also includes under its umbrella the Tata Memorial Hospital (TMH), the largest cancer hospital in Asia. ACTREC has the mandate to function as a national centre for treatment, research and education in cancer. TMC is an autonomous grant-in-aid institution of the Department of Atomic Energy (DAE), Government of India. It is registered under the Societies Registration Act (1860) and the Bombay Public Trust Act (1950). Its Governing Council is headed by the Chairman, Atomic Energy Commission, Government of India.

    Post: Clinical Trial Coordinator

  • Vacancy for Clinical Data Analyst II in Parexel
    Vacancy for Clinical Data Analyst II in Parexel

    PAREXEL has supported the Bio-Tech and Pharmaceutical industries in helping the development of new drugs and treatments on a global basis. As a leading global biopharmaceutical service provider, they supply knowledge-based contract research, medical communications and consulting services across a broad range of therapeutic areas to the worldwide pharmaceutical, biotechnology and medical device industries. They have helped over 800 clients to develop and launch some of the most important drugs and devices of our time-helping people live better and healthier lives everywhere in the world. Headquartered near Boston, Massachusetts, PAREXEL operates in more than 50 countries around the world.

    Post: Clinical Data Analyst II

  • Job for Document Management Associate/Assistant in Icon Clinical Research
    Job for Document Management Associate/Assistant in Icon Clinical Research

    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. We make it our mission to attract the most diverse and creative minds into the business and we continually strive to provide opportunities for our people to excel, grow and build a great career. We understand that our greatest asset is the skills and talents of our people and they are truly what set us apart.

    Post: Document Management Associate/Assistant - 008035

Subscribe to CR