[Hiring] Global Drug Safety Associate @Arriello Ireland Limited

Role Description

This is a remote position.

As a Global Drug Safety Associate, you will support the management of patient safety reports and assist with day-to-day operational activities within the department.

Key Responsibilities

• Management of patient safety reports received via calls and written reports.
• Entry and analysis of safety data to a high-quality standard.
• Translation of safety report information where required.
• Review of safety articles in the public domain.
• Monitoring safety mailboxes and maintaining tracking systems.
• Administrative and documentation support in line with Good Documentation Practice.

You will work closely with colleagues across Global Drug Safety and other departments, gaining exposure to international clients and regulatory standards.

Qualifications

• Native/Fluent German speaker.
• Degree in Life Sciences or a related scientific discipline.
• Experience working in Pharmacovigilance advantageous.
• Strong attention to detail and organisational skills.
• Fluent written and spoken English.
• Interest in building a long-term career in Drug Safety.
• Fluent/Native Romanian advantageous.

Requirements

• Native/Fluent German speaker.
• Degree in Life Sciences or a related scientific discipline.
• Experience working in Pharmacovigilance advantageous.
• Strong attention to detail and organisational skills.
• Fluent written and spoken English.
• Interest in building a long-term career in Drug Safety.
• Fluent/Native Romanian advantageous.

Benefits

• Fully remote working.
• Annual bonus and employee recognition programmes.
• Five weeks' annual leave, plus public holidays and personal days.
• Home office support.
• Career development and professional growth opportunities.
• Exposure to global clients and international projects.
• A collaborative, inclusive, and supportive culture where your contribution is valued.

Company Description

At Arriello, we help pharmaceutical and life sciences organisations navigate complex regulatory requirements while keeping patient safety at the centre of everything we do.

Through our expertise in Pharmacovigilance, Quality & Compliance, and Regulatory Affairs, we support clients across the globe in delivering safe and effective medicines to patients.

We are proud of our supportive and inclusive culture, where people are encouraged to share ideas, develop their expertise, and contribute to continuous improvement.

Our values shape how we work every day:

• Inclusive – We value fairness, respect, and learning from one another.
• Dedicated – We deliver practical, client-focused solutions with excellence.
• Innovative – We collaborate to find smarter and more effective ways forward.
• Passionate – We care deeply about our clients, our colleagues, and the quality of our work.