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  • AstraZeneca Hiring Regulatory Affair Manager

    experience in regulatory affairs or drug development within the pharmaceutical or related industry; Detailed knowledge of the global/regional drug regulatory approval process, submission standards, and health authority requirements
  • AstraZeneca Hiring International CMC Regulatory Affairs Manager
    AstraZeneca Hiring International CMC Regulatory Affairs Manager
    The role holders effectively manage the production of Chemistry, Manufacturing and Control (CMC) documentation for designated product ranges (synthetics/biologics) to deliver the needs of both the AZ business and the customer. AstraZeneca
  • Apply Online for Clinical Data Scientist at AstraZeneca
    Apply Online for Clinical Data Scientist at AstraZeneca

    AstraZeneca (AZ) has a bold aspiration to improve the lives of 200 million patients delivering 20 new medicines to patients by 2030. This role is critical in contributing to AZ’s long-term ambition. Global Business Services (GBS) is growing to support critical functions across the whole Enterprise. This role will be specifically focused on defining and delivering GBS opportunities within the R&D areas of the business. 

    Post : Clinical Data Scientist

  • AstraZeneca Hiring Commercial Pharma Analytics Associate
    AstraZeneca Hiring Commercial Pharma Analytics Associate
    Experience in brand or commercial analytics within pharmaceuticals, healthcare, or another highly regulated industry. AstraZeneca
  • Postdoctoral Fellowships at AstraZeneca
    Postdoctoral Fellowships at AstraZeneca
    Develop and implement advanced in vitro and ex vivo assays to characterize inflammasome-mediated signaling pathways and their impact on myeloid cell differentiation.
  • Work as Trials and Publication Project Manager at AstraZeneca
    Work as Trials and Publication Project Manager at AstraZeneca
    Works in close collaboration with the external service provider and Investigators to ensure quality and quantity commitments are achieved in a timely and efficient manner.
  • Work as Patient Safety QA Advisor at AstraZeneca
    Work as Patient Safety QA Advisor at AstraZeneca
    Knowledge of global and regional pharmacovigilance regulations. Experience in Pharmacovigilance, data management, and adverse event reporting and processing, with proficiency in relevant software tools.
  • Work as Trials and Publication Project Manager at AstraZeneca - Pharm.D Apply
    Work as Trials and Publication Project Manager at AstraZeneca - Pharm.D Apply
    Responsible for ensuring that the study is conducted in accordance with AZ Procedures / Applicable SOPs and Guidelines, such as ICH and GCP as well as relevant local regulations.
  • AstraZeneca Require TMF Team Lead - B.Pharm, BSc Apply
    AstraZeneca Require TMF Team Lead - B.Pharm, BSc Apply
    GBS TMF Team Lead is responsible for the strategic oversight, coordination, and leadership of the GBS TMF Services, ensuring high standards in Trial Master File management and inspection readiness for all assigned clinical trials.
  • Work as Literature Review Advisor at AstraZeneca
    Work as Literature Review Advisor at AstraZeneca
    Literature Review Advisor, you will be at the forefront of ensuring the quality and accuracy of comprehensive literature reviews within the pharmaceutical sector. Pharmacovigilance knowledge excellence. AstraZeneca
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