Pharmacovigilance Reporting Associate (Ciudad de México)

Pharmacovigilance Reporting Associate (Ciudad de México)

01 oct
|
Icon Clinical Research
|
Ciudad de México

01 oct

Icon Clinical Research

Ciudad de México

Pharmacovigilance Reporting Associate (Intelligence)

ICON is a integral 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 Reporting Associate at ICON, you will be responsible for the accurate and timely preparation of safety reports related to clinical trials and post-marketing activities.

What You Will Do:
- Serve as safety reporting intelligence processor and/or lead for multiple safety reporting or safety reporting intelligence stand‑alone projects, providing management support as designated.
- Recognize, exemplify, and adhere to ICON's values, which center around our commitment to People, Clients, and Performance.
- As a member of staff,



the employee is expected to embrace and contribute to our culture of process improvement with a focus on streamlining our processes adding value to our business and meeting client needs.
- Complete all departmental project activities accurately in accordance with ICON SOPs, Study Specific Procedures, regulatory requirements, and client processes.
- Responsible for safety reporting or safety reporting intelligence activities on assigned projects, working in a customer focused approach and an audit and inspection ready mindset.
- Demonstrate skills pertaining to client management, safety reporting, project scope, submission compliance, quality, and budget.

Your Profile
- Bachelor's degree in life sciences, pharmacy, or a related field.
- Experience in pharmacovigilance or drug safety, with an understanding of safety reporting processes and regulatory requirements preferred.
- Excellent attention to detail and organizational skills, with the ability to prepare and review complex safety reports accurately.
- Strong communication and collaboration

📌 Pharmacovigilance Reporting Associate (Ciudad de México)
🏢 Icon Clinical Research
📍 Ciudad de México

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