documentation and utilisation of the signal management system, PV processes and projects and PV or other audits and inspections... industry, at a regulatory agency, clinical research or related medical / healthcare environment. Extensive experience in drug...
Gileadsafety / PV or a related field in the biopharma industry, clinical research, health administration, health policy... development process, Good Clinical Practices (GCP) and Good Pharmacovigilance (GVP), including worldwide PV regulations...
Gileadpossible, together. Job Description FUNCTION: Medical Safety Science (MSS) / Global Therapeutic Area (TA) Safety Scientists... submissions, responses to regulatory agency inquiries, pharmacovigilance (PV) processes and projects, and PV or other audits...
Gileadcollaboration with the Director of Drug Safety, participate in monitoring, review, analyses, interpretation and evaluation... and contribute to the risk evaluation and benefit-risk assessment for the product. In collaboration with the Director of Drug Safety...
MoonLake Immunotherapeutics