Pharmacovigilance Specialist

As a Pharmacovigilance Reporting Specialist at ICON, you will be responsible for the timely and accurate preparation of pharmacovigilance reports, ensuring... Pharmacovigilance Specialist job in Mexico, Mexico City | ICON JUMP TO CONTENT Manage your application Shortlist 0 Search Careers in ICON Careers We encourage our people to seize the opportunity to bring flexibility, innovation and determination to every situation. By doing this, our people build exciting and rewarding careers, deliver results to help bring life-changing medicines and devices to market and maintain ICON’s success as an industry leader. View jobs at ICON About Icon Overview of Service Lines Job Categories ICON Full Service Full Service Full-service roles offer the opportunity to work on projects and programmes on behalf of the world’s most innovative pharma, biotech and medical device companies. 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View roles Recruitment Process Inside ICON About ICON Our Culture & Our People Our Mission & Values Overview of Service Lines Full Service Strategic Solutions (FSP) Global Business Services Accellacare Site Network ICON Biotech ICON Leadership Our Locations Our Locations With headquarters in Dublin, Ireland, ICON has employees in 119 locations across 53 countries. View roles Global Office Locator Ireland Asia Pacific Australia China India Japan Korea Malaysia Taiwan Europe, Middle East & Africa Belgium Bulgaria Germany Hungary Italy Netherlands Poland Romania Slovakia South Africa Spain Türkiye United Kingdom United States Latin America Argentina Brazil Chile Colombia Mexico Global Office Locator Why ICON? Why ICON? No matter what part of ICON you work in, you are contributing to solving some of the most complex healthcare challenges and are helping to deliver new medicines and devices that are impacting millions of peoples’ lives, right across the world. 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ICON is committed to recruiting top talent while also fostering a culture of learning and development within the organization. Building a Successful Clinical Research Resume Landing Your First Job in Clinical Research Internships Graduate Opportunities Hints & Tips for Graduates graduate What does full service mean for you? Integer posuere erat a ante venenatis dapibus posuere velit aliquet. Duis mollis, est non commodo luctus, nisi erat porttitor ligula. Read more Career Resources Our Culture Application Process AI Usage Policy Our Mission & Values Pharmacovigilance Specialist Location: Mexico City Reference: JR153641 Categories Drug Safety __vacancyopjusttionswidget.opt-Business Area__ ICON Strategic Solutions (FSP) __vacancyopjusttionswidget.opt-Remote Working __ Remote or Office About the role This vacancy has now expired. Please click here to view live vacancies. Home Based - CDMX At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise. As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide. As a Pharmacovigilance Reporting Specialist at ICON, you will be responsible for the timely and accurate preparation of pharmacovigilance reports, ensuring compliance with regulatory requirements and internal policies. What You Will Do: You will contribute to pharmacovigilance and drug safety activities, taking responsibility for your deliverables and working collaboratively. Key responsibilities include: Preparing and submitting comprehensive safety reports, including periodic safety update reports (PSURs) and individual case safety reports (ICSRs), in compliance with regulatory standards. Conducting thorough data analysis to identify trends and assess the safety profile of pharmaceutical products. Collaborating with cross-functional teams to ensure timely and accurate reporting of adverse events. Maintaining up-to-date knowledge of pharmacovigilance regulations and industry best practices to ensure compliance. Providing training and support to team members on pharmacovigilance reporting processes and requirements. Your Profile: You will bring relevant pharmacovigilance and drug safety experience, along with the following qualifications and skills. Required qualifications and experience: Bachelor's degree in a relevant scientific discipline or healthcare-related field Significant experience in pharmacovigilance reporting or drug safety within a clinical or pharmaceutical environment. Strong analytical skills with proficiency in data analysis tools and reporting software. Excellent communication and interpersonal skills, facilitating effective collaboration with internal and external stakeholders. A commitment to maintaining high standards of quality and compliance in all pharmacovigilance activities. 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 additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our benefits examples include: Various annual leave entitlements A range of health insurance offerings to suit you and your family’s needs. Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to 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. Visit our careers site to read more about the benefits ICON offers. 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, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles. Are you a current ICON Employee? Please click here to apply Share: Hi, I am Rita and I manage this role TA Business Partner Icon Strategic Solutions View my profile Email [email protected] View my other roles Send me a message First Name * Last Name * Email address * Enquiry * Send Cancel Get Job Alerts! Sign up to receive job updates tailored to your interests. Sign Up Not Ready to Apply? Join our Talent Community for future alerts. Sign up Explore more about ICON About ICON Explore Global Office Locator Explore Benefits & Rewards Explore Inclusion & Belonging Explore Career Pathways Explore Environmental, Social & Governance Explore List #1 Day in the life What does a Drug Safety Associate (DSA) do? Teaser label Inside ICON Content type Blogs Publish date 09/29/2022 Summary A Drug Safety Associate is responsible for assessing the safety of pharmaceuticals drugs once they’re on the market. Using standardised guidelines, they determine whether the medication causes any adv Teaser label A Drug Safety Associate is responsible for assessing the safety of pharmaceuticals drugs once they’re on the market. 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