Drug Safety Associate
ICON is a global 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 Drug Safety Associate at ICON, you will ensure the safety of investigational drugs and contribute to the advancement of innovative treatments and therapies for one of our valued sponsors.
What You Will Do:
Your role will involve delivering pharmacovigilance and drug safety work to a high standard, working closely with your team and stakeholders.
Key responsibilities include:
- Collect and review adverse event reports from clinical trials and post-marketing sources.
- Conduct initial assessment and coding of adverse events according to established procedures and regulatory guidelines.
- Prepare and submit expedited safety reports to regulatory authorities and investigators as required.
- Assist in the development and maintenance of safety databases and tracking systems.
- Collaborate with cross-functional teams to ensure timely and accurate reporting of safety data.
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 scientific or healthcare-related field.
- 1-2 years of experience in pharmacovigilance or drug safety within the pharmaceutical or biotechnology industry preferred.
- Knowledge of pharmacovigilance regulations and guidelines (e.g., ICH, FDA, EMA).
- Strong attention to detail and ability to work effectively in a fast-paced environment.
- Excellent communication and organizational skills, with the ability to collaborate across teams and prioritize tasks efficiently.
- Willingness to travel as required (approximately 10%)
LI-SB2
Employment with ICO
📌 Drug Safety Associate (Milano)
🏢 Ire
📍 Milano