Life Sciences Job at ICON as Pharmacovigilance Associate | Apply Now
Looking for a rewarding Life Sciences Job in pharmacovigilance? ICON plc is hiring a Pharmacovigilance Associate in São Paulo. This opportunity is ideal for candidates interested in drug safety, regulatory compliance, and post-marketing surveillance. Explore how this Pharmacovigilance Associate Job at ICON careers can help you build a strong future in clinical research and healthcare intelligence.
- Job Position: Pharmacovigilance Associate
- Location: São Paulo, Brazil (Remote)
- Job ID: JR144408
About the Company
ICON plc is a world-leading healthcare intelligence and clinical research organization. The company is known for fostering an inclusive environment that drives innovation and excellence. ICON is committed to shaping the future of clinical development while maintaining high standards in patient safety and compliance. This makes ICON careers a top choice for professionals seeking a Life Sciences Job.
Job Description
ICON is currently seeking a Pharmacovigilance Associate – Post Marketing to join its dynamic team. In this Pharmacovigilance Associate Job at ICON careers, you will play a vital role in monitoring and ensuring the safety of pharmaceutical products. The position involves collecting, analyzing, and reporting adverse event information while ensuring compliance with regulatory standards.
This Life Sciences Job offers an excellent opportunity to contribute to patient safety and gain hands-on experience in drug safety and pharmacovigilance.
Qualifications
This Life Sciences Job Role requires:
- Bachelor’s degree in life sciences or a related field; advanced degree preferred
- Experience in pharmacovigilance, drug safety, or a related area, preferably within a clinical or pharmaceutical environment
- Strong analytical skills with attention to detail in data collection and reporting
- Excellent communication and interpersonal skills for effective collaboration
- Commitment to maintaining high standards of quality and compliance
Key Responsibilities
This Life Sciences Job Role responsibilities include:
- Collecting and reviewing adverse event reports to ensure accurate and timely reporting in accordance with regulatory guidelines
- Conducting signal detection and risk assessment activities to identify potential safety issues
- Collaborating with cross-functional teams to support safety-related inquiries and investigations
- Maintaining up-to-date knowledge of pharmacovigilance regulations and industry best practices
- Assisting in the preparation of safety reports and regulatory submissions
Benefits of Joining this Life Sciences Job
- Competitive salary package
- Various annual leave entitlements
- Health insurance options for you and your family
- Retirement planning benefits
- Global Employee Assistance Programme (LifeWorks)
- Life assurance
- Flexible benefits including childcare vouchers, gym memberships, and travel passes
