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Pharmacovigilance

academics

 

Clinical research courses

  • Require SERM Scientific Director at GSK

    Leads Pharmacovigilance and Risk Management Planning and develops strategy for approach to evaluation of issues in the clinical matrix. Leads the safety component of global regulatory submissions.
  • Hiring Pharmacovigilance Associate & MICC Associate at Arcolab - B.Pharm, M.Pharm, Pharm.D Apply
    B.Pharm, M.Pharm, Pharm.D or BDS.; Working knowledge of literature case processing, drug safety regulations and adverse event reporting
  • Work as Pharmacovigilance Specialist at Baxter
    Ensure that the correct suspect drug was selected within the Pharmacovigilance Safety System; Code medical terms using standardized medical dictionaries i.e. MedDRA Using medical expertise, ensure that all data has been entered and coded correctly in the Global Safety Database
  • Pfizer Hiring Safety Surveillance Sr. Associate

    Pfizer is the world's premier biopharmaceutical company taking new approaches to better health.  We discover, develop, manufacture and deliver quality, safe and effective prescription medicines to treat and help prevent disease for both people and animals. We also partner with healthcare providers, governments and local communities around the world to expand access to our medicines and to provide better quality health care and health system support.  

    Post : Sr. Associate - Safety Surveillance

  • Work as Pharmacovigilance Manager at Teva
    Oversee and ensure all EMIA/APAC Regional PV Operations Hub Key Performance Indicators are completed in a timely manner, with high quality, and in compliance with worldwide regulatory and Global PV requirements.
  • Work as Pharmacovigilance Services Analyst at Accenture
    Your day to day interaction is with peers within Accenture before updating supervisors. In this role you may have limited exposure with clients and/or Accenture management.
  • Work as Pharmacovigilance Specialist at ICON plc

    ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life. Our people are our greatest strength, are at the core of our culture, and the driving force behind our success.

  • Require Pharmacovigilance Associate at Teva

    Teva is on a mission to make good  health more affordable and accessible, to help millions around the world enjoy healthier lives. It’s a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world’s leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization’s Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day.

  • Teva looking for Pharmacovigilance Associate - B.Pharm, M.Pharm, Pharm.D Apply
    Data retrieval for authoring and preparation of selected PSUR sections. Review, QC of the data retrieval procedure and selected PSUR sections.
  • Novotech looking for Drug Safety Associate
    Knowledge of clinical trials and pharmacovigilance requirements. Knowledge, experience in international drug safety-regulatory reporting obligations and compliance. 
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