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  • Fortrea Hiring Proposals Apprentice

    The Apprentice participates in and executes the entry level department functions (Designation of Apprentice) in accordance with Fortrea and/or sponsor Standard Operating Procedures (SOPs)
  • ICON plc Hiring Graduate Pharmacovigilance Associate
    Bachelors degree in pharmacy, life sciences, or a related field. Basic understanding of pharmacovigilance principles and regulatory guidelines is desirable but not required; relevant training will be provided. ICON plc
  • ProPharma Hiring Medical Information Specialist
    The Medical Information Specialist (MIS) position is part of the ProPharma Medical Information Contact Center and follows all corresponding regulations, industry standards, and client/internal policies regarding medical information and the collection and documentation of adverse events, special situation events, and product complaints.
  • Research Recruitment at BITS Hyderabad - Pharma candidates Apply

    Applications are invited for the position of one Project Research Scientist I in the Department of Biological Sciences at BITS Pilani, Hyderabad Campus, Hyderabad, for an ICMR-sponsored research project titled "A target-guided approach for design, synthesis, and screening of host-directed therapies for TB and associated metabolic disorders (PCOS) in women."

    Post : Project Research Scientist I

  • Work as Senior Regulatory Affairs Associate at PAREXEL
    Contribute to the preparation (including authoring, where relevant) and delivery of simple regulatory maintenance submissions and, with experience, increasingly complex submissions from a global and/or regional perspective.
  • Apply Online for initiation Clinical Research Associate at PAREXEL
    Seeking an Initiation Clinical Research Associate II (Site Start Up EUCTR II) to join our team in a Hybrid capacity at our Hyderabad office. As an Initiation Clinical Research Associate II, you will support complex clinical trial initiation activities that advance new treatments for patients.
  • Safety Science Specialist Require at Fortrea
    Data entry of safety data onto adverse event database and tracking systems.Review of adverse events for completeness, accuracy and appropriateness for expedited reporting.
  • Sun Pharma Hiring Clinical Quality & Process Manager
    Reviews, develops, and supports implementation of SOPs, controlled documents, and training programs relevant to Sponsor Oversight and RBQM.
  • Apply Online for Drug Safety Specialist at Medpace
    Office-based Clinical Safety Coordinator to join our Clinical Safety department in India. This position will be focused on the handling and processing of adverse events from all sources, including clinical trials and post marketing surveillance.
  • Require Manager Regulatory Affairs at Boehringer Ingelheim
    Bachelors degree in pharmacy or similar medical education. Pharma experience with regulatory focus in a multi-national
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