A global clinical research organization is seeking a Senior Associate, Pharmacovigilance to oversee the collection, processing, and reporting of adverse event data. This role is essential for ensuring compliance with regulatory guidelines and leading safety evaluations in complex studies. Candidates must possess a Bachelor's degree and at least 5 years of pharmacovigilance experience. Strong organizational and communication skills are crucial. The position offers a remote work opportunity based in Mexico City.
#J-18808-Ljbffr