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  • Apply Online for Associate Data Manager at Medpace

    Bachelors degree with clinical Data Management experience, including managing multiple clinical projects and serving as the primary sponsor contact.
  • Require Associate Pharmacovigilance Manager at Novo Nordisk
    Require Associate Pharmacovigilance Manager at Novo Nordisk
    Responsible for leading and overseeing local pharmacovigilance activities, including adverse event case processing, safety reporting to Health Authorities, customer complaint handling, regulatory compliance, data quality, and stakeholder collaboration across clinical development and post-marketing activities.
  • Work as Safety Data Sheets Expert at Sanofi
    Work as Safety Data Sheets Expert at Sanofi
    Bachelors degree in Biological Science (biology, microbiology, Molecular Biology) or technical discipline at minimum.
  • GSK looking for Senior Scientist Pharmacovigilance
    GSK looking for Senior Scientist Pharmacovigilance
    Experience in Pharmacovigilance and Medical Information regulatory requirements, systems, and processes
  • Vacancy for MPharm, MSc in Analytical R&D Lab at FDC Limited
    Vacancy for MPharm, MSc in Analytical R&D Lab at FDC Limited
    Good knowledge in analytical instrumentation commonly used in pharmaceutical testing such as HPLC, UV, Dissolution, FTIR and Karl-Fisher.
  • Emcure Interview : Roles in Quality Control, Production, Packing
    Emcure Interview : Roles in Quality Control, Production, Packing
    QC -Reviewer Preference will be given to candidates having hands-on experience on Waters HPLC systems with Empower software. 
  • Apply Online for Regulatory Affairs Manager at IQVIA
    Apply Online for Regulatory Affairs Manager at IQVIA

    IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. 

    Post : Regulatory Affairs, Manager

  • Apply Online for Safety & PV Specialist post at Syneos Health
    Apply Online for Safety & PV Specialist post at Syneos Health
    Maintain safety tracking systems and ensure timely completion of assigned activities and deliverables. Conduct MedDRA coding, drug coding, and maintenance of drug dictionaries as required.
  • Require Team Lead at Astellas Pharma Inc
    Require Team Lead at Astellas Pharma Inc
    The Lead is expected to have extensive experience and provide thought leadership in Data Governance and Compliance, as well as on how the regulatory and pharmacovigilance (safety) systems, processes, and data interact and interface with other aspects of the Astellas information ecosystem.
  • Sun Pharma Openings in MS&T Department
    Sun Pharma Openings in MS&T Department
    Responsible for executing technology transfer activities for solid oral dosage forms, including planning and performing Scale-up, Exhibit and Process Validation batches with optimal utilization of manpower, materials and equipment.
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