This is a remote position.

Advancing patient safety. Building trusted partnerships. Growing careers.

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. As our business continues to grow, we are looking for talented professionals who are passionate about quality, collaboration, and making a meaningful impact.

We are proud of our supportive and inclusive culture, where people are encouraged to share ideas, develop their expertise, and contribute to continuous improvement. If you are looking for an opportunity to apply your skills in a dynamic international environment while continuing to build your career, we would love to hear from you.

Our Values

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.

The opportunity

Global Drug Safety Associate

Are you a native/fluent German speaker with a degree in a Life Science discipline and experience in working in the pharmacovigilance envirnoment?

Arriello is expanding its Global Drug Safety team and we are looking for an Associate level professional who is ready to learn, contribute, and grow within Pharmacovigilance.

What you will do

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.

Requirements

Essential

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.

Equal Opportunities

Arriello is committed to creating a diverse, inclusive, and respectful workplace where everyone can thrive. We welcome applications from all backgrounds and are dedicated to providing reasonable accommodations throughout the recruitment process for candidates who require support.

Learn more about this Employer on their Career Site