Drug Safety Associate

This is a fully remote position, open to applicants in Italy, +2 more states.

📋 Description

• Gather and analyze adverse event reports from clinical trials and post-marketing sources.

• Perform initial evaluations and coding of adverse events in accordance with established protocols and regulatory standards.

• Prepare and submit expedited safety reports to regulatory bodies and investigators as necessary.

• Support the creation and upkeep of safety databases and tracking systems.

• Work collaboratively with cross-functional teams to ensure timely and accurate reporting of safety information.

⛳️ Requirements

• A bachelor's degree in a scientific or healthcare-related discipline.

• 1-2 years of experience in pharmacovigilance or drug safety in the pharmaceutical or biotechnology sector is preferred.

• Familiarity with pharmacovigilance regulations and guidelines, including ICH, FDA, and EMA.

• Strong attention to detail and the ability to thrive in a fast-paced environment.

• Exceptional communication and organizational skills, with the capability to collaborate across teams and prioritize tasks effectively.

• Willingness to travel as necessary, approximately 10%.

• Legal authorization to work in the country where the position is located.

🏝️ Benefits

• Competitive base salary along with performance-based incentives.

• Health and wellness programs, including medical, dental, and vision coverage where applicable.

• Retirement and pension plans.

• Life insurance and disability coverage.

• Employee assistance programs and wellness resources.

• Opportunities for learning and development through structured training and career pathways.