Summarized Purpose:Performs day-to-day Pharmacovigilance (PV) activities performed within a highly regulated environmentand driven by strict timelines.Pharmacovigilance activities include but are not limited to collection,monitoring, assessment, evaluation, research and tracking of safety information.Coordinates andperforms Pharmacovigilance activities such as data entry, coding and assessment of adverse events, casereview, follow-up, tracking of reports, and regulatory reporting activities.Effectively collaborates withvarious parties such as: project team members, client contacts, investigators, and adverse event/reporters, and third party vendors.May assist in the preparation of departmental and project-specificprocedures and processes, prepare for and attend audits, kick-off and investigator meetings.Essential FunctionsPerforms day-to-day PV activities.May participate in on-call duties for specificprojects to ensure 24-hr coverage for intake of cases from investigative sites.Reviews regulatory/pharmacovigilance publications and information sources to keep updated on current regulations, practices, procedures and proposals.Maintains medical understanding of applicable therapeutic area and diseasestates.Reviews cases entered for quality, consistency and accuracy, including review of peer reports.Prepares and maintains regulatory safety reports.Assists with routine project implementation and coordination (e.g., Clinical Trials, Endpoint Assessment Committee/Data Safety Monitoring Committee),



including presentations at client/investigator meetings, and review of metrics and budget considerations.Mentors less experienced staff.Qualifications:Education and Experience:Bachelor's degree or equivalent and relevant formal academic / vocational qualification Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2+ years).
In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.Knowledge, Skills and Abilities:General understanding of pathophysiology and the disease processDetailed knowledge of relevant therapeutic areas as required for processing AEsStrong critical thinking and problem solving skillsGood oral and written communication skills including paraphrasing skillsGood command of English and ability to translate information into local language where requiredComputer literate with the ability to work within multiple databasesPrevious exposure to Microsoft Office packages (including Outlook, Word, and Excel)Understanding the importance of and compliance with procedural documents and regulationsAbility to manage and prioritize a variety of tasks and meet strict deadlines with limited supervisionStrong attention to detailAbility to maintain a positive and professional demeanor in challenging circumstancesAbility to work effectively within a team to attain a shared goal

📌 Safety Specialist (Xico)
🏢 Thermo Fisher Scientific
📍 Xico