A recruitment firm for a multinational company seeks a remote Pharmacovigilance Associate responsible for managing safety cases from clinical trials. The role requires accurate documentation, evaluation, and compliance with global regulations. Candidates should have a Bachelor's in Life Sciences and at least 1 year in pharmacovigilance case processing. Familiarity with safety reporting and clinical documentation is essential, along with strong attention to detail and regulatory awareness.
#J-18808-Ljbffr