OVERVIEW The Associate Safety Case Reviewer collaborates with the Pharmacovigilance Solutions Production team to analyze and report on safety parameters within the context of patient safety against our clients’ products, and in line with client requirements for case review. DESCRIPTION • Perform various tasks in support of our clients’ clinical research including: adverse event analysis and processing • Prepare safety reports for submission to various health authorities • Maintain data integrity and promote audit compliance by following Good Documentation Practice (GDP) standards • Adhere to project timelines, with proactive communication with Team Lead and Project Managers, as needed • Understand and comply with appropriate conventions and other governing bodies following applicable divisional guidelines, templates, and Standard Operating Procedures (SOPs) • Analyze stakeholder complaints related to safety reporting, address in real time, and discuss with Project Managers to mitigate risk and implement/drive solutions • Complete all other tasks that are deemed appropriate for this role and assigned by the manager/supervisor REQUIRED SKILLS • Knowledge of Common Toxicity Criteria (CTC) and/or MedDRA coding • Knowledge of Good Clinical Practice (GCP), Good Documentation Practice (GDP), and International Conference on Harmonization (ICH) guidelines • Proficiency in Word, PowerPoint, Excel, Outlook, EndNote, and scientific databases including PubMed, Embase, etc. • Excellent written and oral communication skills in English • Ability to work in collaborative, cross-functional teams • Ability to meticulously review and validate work to ensure strict compliance with SOPs and client specifications