As a Safety Specialist, you’ll perform day-to-day Pharmacovigilance (PV) activities within a highly regulated environment driven by strict timelines. Your responsibilities will include the collection, monitoring, assessment, evaluation, research, and tracking of safety information. You will coordinate and perform PV activities such as data entry, coding, assessment of adverse events, case review, follow-up, tracking of reports, and regulatory reporting activities. You will effectively collaborate with various parties such as project team members, client contacts, investigators, adverse event reporters, and third-party vendors. You may assist in the preparation of departmental and project-specific procedures and processes, and prepare for and attend audits, kick-off, and investigator meetings.<\/p>\n","protected":false},"author":2334,"featured_media":0,"comment_status":"closed","ping_status":"closed","template":"","job_listing_type":[66],"job_listing_category":[],"job_listing_location":[531],"job_listing_tag":[],"job_listing_employer_type":[371],"job_listing_specialization":[528],"class_list":["post-45261","job_listing","type-job_listing","status-publish","hentry","job_listing_type-full-time","job_listing_location-taguig","job_listing_employer_type-others","job_listing_specialization-pharmacist"],"yoast_head":"\n