Pharmacovigilance Specialist (PV Lead) - Mexico - Office with Flex
ICON is a general healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
As a Pharmacovigilance Specialist at ICON, you will be responsible for monitoring the safety of pharmaceutical products by analyzing, interpreting, and reporting adverse event data in accordance with regulatory requirements.
What You Will Do:
Key responsibilities include:
- Collecting, reviewing, and analyzing adverse event reports to ensure timely and accurate reporting in compliance with regulatory guidelines.
- Conducting risk assessments and signal detection activities to identify and evaluate potential safety concerns.
- Collaborating with cross-functional teams to support safety-related inquiries and investigations.
- Preparing and submitting safety reports and regulatory submissions in a timely manner.
- Staying current on pharmacovigilance regulations and industry best practices to enhance the safety framework.
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
- 4+ Years of experience in pharmacovigilance, drug safety, or a related area, preferably within a clinical or pharmaceutical setting.
- Proven experience as PV lead
- Strong analytical skills and attention to detail in data collection and reporting.
- Excellent communication and interpersonal skills, enabling effective collaboration with diverse teams.
- A commitment to upholding high standards of quality and compliance in all pharmacovigilance activities.
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Employment with ICON
📌 Pharmacovigilance Specialist (Ciudad de México)
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📍 Ciudad de México
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