Pharmacovigilance Associate at ICON plc – Apply Now!
Looking to advance your career in drug safety and regulatory compliance? Join ICON plc as a Pharmacovigilance Associate and play a key role in ensuring patient safety and regulatory excellence. Based remotely in Bogotá, this role offers an opportunity to work with a global leader in clinical research, contributing to life-changing therapies and medicines across the globe.
- Job Title: Pharmacovigilance Associate
- Location: Bogota, Colombia
- Job Reference: JR131258
About The Company
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.
About the Role:
We are currently seeking a Pharmacovigilance Associate to join our diverse and dynamic team. As a Pharmacovigilance Associate at ICON, you will play a vital role in monitoring and ensuring the safety of pharmaceutical products by collecting, analyzing, and reporting adverse event information. Your attention to detail and understanding of regulatory requirements will be essential in supporting the organization’s commitment to patient safety and compliance.
Job Description
Key Responsibilities:
- Collect, review, and process adverse event (AE) reports in compliance with global regulatory guidelines.
- Perform signal detection, risk assessment, and case triaging for potential safety issues.
- Prepare and contribute to the development of safety reports and regulatory submissions.
- Collaborate with medical writers, regulatory affairs, and clinical teams on pharmacovigilance strategies.
- Stay updated with local and international pharmacovigilance regulations (e.g., EMA, FDA, ICH, MedDRA).
Your Profile:
- Education: Bachelor’s in Life Sciences, Pharmacy, or a related field (advanced degree preferred).
- Experience: Minimum 1–2 years in pharmacovigilance, drug safety, or medical affairs, ideally within clinical trials or a pharmaceutical company.
- Strong attention to detail with sound knowledge of pharmacovigilance processes.
- Proficient in safety databases (e.g., Argus, ArisG) and electronic reporting systems.
- Excellent communication and organizational skills.
Why Join ICON?
ICON plc is a global healthcare intelligence and clinical research organization, working at the forefront of drug development and regulatory strategy. Our diverse teams span over 40 countries, delivering high-quality solutions that accelerate product pipelines for biopharma and medical device clients.
ICON Employee Benefits:
- Flexible remote work model
- Generous annual leave allowances
- Comprehensive health and life insurance plans
- Global Employee Assistance Program (LifeWorks)
- Retirement planning support
- Access to wellness benefits: gym memberships, health assessments, and more
Keywords: Pharmacovigilance, Associate, Drug Safety, Job Opportunity, Clinical Development, Regulatory, Patient Safety, Compliance
