Spyre Therapeutics - Director, Drug Safety Physician

• Perform triage and medical review of ICSRs (in and/or outside the global safety database), and oversight of cases/AOSE for expedited safety reporting • Lead cross-functional medical review discussions pertaining to Individual Case Safety Report (ICSR) review • Participate in the preparation, writing, and/or review of aggregate safety review documents (DSUR) and safety sections of relevant clinical trial documents and regulatory filings • Participates in and/or leads review of scientific literature, including preparation of written summaries to support aggregate safety analyses • Participate in safety data review including safety surveillance activities and the evaluation & management of safety signals emerging from any data source • Participate and co-present cases at safety management team (SMT) and safety review team (SRT) meetings and co-lead safety surveillance and signal management meetings • Participate in process improvement projects related to medical review and assessment, safety surveillance, and relevant aspects of PV compliance • Assist the DSPV department head in developing and maintaining state-of-the-art Pharmacovigilance (PV) processes and procedures including SOPs, WI, safety management plans, and safety surveillance plans • Participate in safety presentation development for independent Data Monitoring Committee (iDMC) meetings • Collaborate closely and assists the Medical Review Lead and other physicians on the team on the ongoing review of cases and in developing a unified approach for medical review of ICSRs, safety presentations (relevant to medical review of ICSRs and/or safety surveillance aspects), and provides ongoing input into study protocols, periodic safety reports (DSURs), safety management plans etc.  Lead epidemiology projects with relevance for safety and pharmacovigilance (natural history of disease, comorbidities, class effects, population health data, real-world drug safety monitoring, literature searches, signal detection and data mining, comparative effectiveness and safety research) • Ensure that all assigned activities are executed efficiently commensurate with quality, accuracy, and timeliness and in accordance with current global regulatory requirements • Provide medical safety strategy and execution of benefit-risk management strategies for assigned products • Provide safety input to clinical development plans, responses to HA or institutional review board/ ethics committee queries • Provide input into the development of safety risk language, risk management strategy, pre-filing safety activities including safety table shells, integrated safety data review, integrated safety summary document review, and safety-focused publication development • Other duties as assigned