Pharmacovigilance Specialist

Job OverviewUnder moderate supervision, executes the feasibility, site identification regulatory, start-up, and maintenance activities in accordance with regulations, SOPs, and project requirements at the regional, or country level.Essential FunctionsPharmacovigilance processes applicable to RSU.Submission of safety reports (periodic and expedited).Submission of SAE / SUSAR to RA on time for the applicable studies according to regulatory timelines.Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and / or international regulations, standard operating procedures (SOPs), project requirements, and contractual / budgetary guidelines.May also include maintenance activities.QualificationsBachelor's Degree in Life Sciences or a related field.1 - 2 years of pharmacovigilance experience in clinical studies.Fluent conversational English.#J-18808-Ljbffr