[Hiring] Clinical Safety Specialist @Arriello Ireland Limited

Role Description

As a Clinical Safety Specialist, you will play an important role in helping our clients maintain the highest standards of patient safety throughout the product lifecycle. This is an excellent opportunity for an experienced pharmacovigilance professional who enjoys combining technical expertise, project coordination, stakeholder collaboration, and continuous improvement.

Working within our Global Drug Safety team, you will take ownership of key safety activities, support complex client projects, and act as a trusted partner to both internal and external stakeholders. You will have the opportunity to contribute across a wide range of pharmacovigilance and drug safety activities while helping to shape processes, mentor colleagues, and drive quality across projects.

If you are motivated by making a meaningful contribution to patient safety and are looking for a role where your expertise will have real impact, we would love to hear from you.

Qualifications

• Bachelor's degree in Pharmacy, Pharmaceutical Sciences, Life Sciences, Medicine, or a related discipline.
• Minimum 3 years of experience within pharmacovigilance, drug safety, or a related safety environment.
• Strong knowledge of Drug Safety regulations, processes, and industry guidelines including ICH, GVP, GCP, and CIOMS.
• Experience working with safety databases.
• Experience managing multiple priorities while maintaining a high standard of quality and compliance.
• Strong project coordination and stakeholder management skills.
• Experience working cross-functionally with internal and external stakeholders.
• Excellent communication and organisational skills.
• Fluent written and spoken English.
• A collaborative approach and a passion for continuous improvement.

Requirements

• Experience with Veeva Vault Safety.
• Experience across both clinical trial and post-marketing environments.
• Experience supporting client-facing projects in a consultancy, CRO, or service-based environment.
• Experience contributing to audits, inspections, and CAPA management.

Benefits

• Flexible working arrangements.
• Opportunities for professional development and career progression.
• Exposure to international clients and diverse project portfolios.
• A collaborative and supportive culture built on knowledge-sharing and teamwork.
• The opportunity to work alongside leading pharmacovigilance and regulatory experts.
• Meaningful work that directly contributes to patient safety and public health.
• Recognition for your expertise, contributions, and achievements.

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.
• Innovative – We work together to find better ways forward.
• Passionate – We build strong relationships and care about the quality of what we do.