Pharmacovigilance Associate / Senior Associate ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. We are currently seeking a Senior Pharmacovigilance Associate to join our diverse and dynamic team. As a Senior Pharmacovigilance Associate at ICON, you will be instrumental in ensuring the safety and efficacy of pharmaceutical products by managing and overseeing pharmacovigilance activities. You will collaborate with cross‑functional teams to ensure compliance with regulatory requirements and to maintain the highest standards of patient safety. Location: Mexico City Contract type: Hybrid (office‑based with flexibility) Requirement: CVs and assessments must be submitted in English. What You Will Be Doing Leading the collection, evaluation, and processing of adverse event reports to ensure timely and accurate reporting in accordance with regulatory guidelines and company policies. Conducting thorough data analysis and interpretation of safety data, identifying trends and potential safety signals that require further investigation. Preparing and submitting comprehensive periodic safety update reports (PSURs) and other regulatory documents, ensuring compliance with international regulations. Collaborating with medical and clinical teams to assess the clinical relevance of reported adverse events and contributing to risk management activities. Overseeing the maintenance and integrity of pharmacovigilance databases, ensuring accurate documentation and compliance with data management standards. Providing training and mentorship to junior team members on pharmacovigilance processes, regulatory requirements, and best practices. Engaging in audits and inspections conducted by regulatory authorities, ensuring readiness and compliance with all relevant pharmacovigilance requirements. Staying informed on evolving regulatory guidelines and industry best practices to continually enhance the pharmacovigilance processes within the organization. Your Profile Bachelor’s degree in life sciences, pharmacy, nursing, or a related field. An advanced degree is preferred. Experience in leading PV studies or projects (REQUIRED). Extensive experience in pharmacovigilance or drug safety, with a strong understanding of relevant regulations and industry standards. Proven ability to manage the pharmacovigilance process effectively, including adverse event reporting and signal detection. Strong analytical and critical thinking skills, with the ability to interpret complex data and make informed recommendations. Excellent communication and interpersonal skills, with the ability to work collaboratively across cross‑functional teams. Proficiency in pharmacovigilance databases and data management systems, as well as Microsoft Office Suite. Ability to work independently and manage multiple priorities in a fast‑paced environment. Commitment to maintaining confidentiality and handling sensitive patient information with discretion. What ICON Can Offer You Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of benefits focused on well‑being and work‑life balance opportunities for you and your family. Various annual leave entitlements. Health insurance offerings to suit you and your family’s needs. Competitive retirement planning offerings to maximize savings and plan with confidence for the future. Global Employee Assistance Programme, LifeWorks, offering 24‑hour access to a global network of over 80,000 independent specialized professionals who support you and your family’s well‑being. Life assurance. Flexible country‑specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others. At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of this position, please let us know. #J-18808-Ljbffr