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Job description:Participates in applicable safety surveillance activities for assigned products; and in planning and completion of AdHoc Safety Reports as needed.Timely assessment of adverse event coding for consistency and accuracy of coding and ; accurate and effective medical review of safety related CRFs and labs, including communication with Study Designated Physicians by interfacing with study manager, Clinical Research Organizations, Clinical Research Associates, Data Management, Pharmacovigilance and others to assure query resolution.Supervise tracking of safety related queries to Investigators and assists in handling safety questions from IRB/IEC.Assist with Study Safety Review Plan development and implementation in collaboration with Study Designated Physicians and provides Safety overview to Clinical team members, Clinical Research Organizations, Investigators and investigator sites as needed and review study protocols, IND reports, annual reports, Investigator Brochures, Safety sections of the Clinical Reports, Monitoring Plans, IDMC data and other ad hoc reports which include safety data.Create narratives of serious adverse events and other identified events of interest in accordance with accepted standards and with high degree of competency.Apply knowledge of ICH, FDA, EMA regulations and guidelines affecting drug and disease state, understanding issues to assigned responsibilities with an in depth understanding of product labeling/literature, including safety profile. Understand, implements and improves department SOPs. Clinical knowledge to apply to adverse event data collection and assessment.May serve as a representative for Safety Management on cross functional projects, but does not assume decision makingresponsibilities in the representative role; Contacts may include Clinical Safety Manager and a variety of multidisciplinary representatives (e.g. Regulatory Affairs, Quality Assurance, Compliance).