Global Drug Safety Manager

At Arriello, we provide Pharmacovigilance, Quality & Compliance, and Regulatory Affairs services to global pharmaceutical and life sciences companies, helping them meet regulatory requirements and protect patient safety.

We are a growing business with a collaborative culture focused on high‑quality delivery, continuous improvement, and giving people the space to do their best work.

Our values guide how we work:

• 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

The Opportunity

This is a fully remote opportunity supporting ongoing portfolio growth and increasing project demand. The role is offered as a 12‑month fixed‑term contract, with a strong possibility of extension for a further 12 months.

You will join a structured and experienced Global Drug Safety team, taking a senior role across technical delivery, people leadership, and client engagement. This position is well suited to a confident, outspoken pharmacovigilance leader who enjoys challenge, can think quickly, and is comfortable operating in complex, fast‑moving environments.

Main Purpose of the Role

You will lead technical delivery across Global Drug Safety projects while providing line management, guidance, and support to team members. You will own project governance, ensure high‑quality and compliant outputs, and drive continuous improvement across systems, processes, and service delivery.

What You Will Do

Leadership & People Management

• Lead, mentor, and line manage Global Drug Safety team members
• Create a high‑performance, supportive environment built on trust, empathy, and accountability
• Act as a calm escalation point and mediator when challenges arise

Project & Programme Delivery

• Lead end‑to‑end Global Drug Safety project delivery across clinical and post‑marketing phases
• Own project scoping, planning, governance, and delivery against timelines and expectations
• Act as Project Manager as required, ensuring high‑quality outcomes

Technical & Scientific Oversight

• Oversee aggregate reporting, safety documentation, and medical writing activities
• Support safety data management, signal detection, and benefit–risk assessments
• Ensure compliance with global regulatory requirements including ICH, GVP, and GCP.

Stakeholder & Commercial Engagement

• Engage confidently with senior internal and external stakeholders
• Participate in bid defences, proposals, and client discussions
• Provide analytical challenge and solution‑driven input to support decision making

Governance & Continuous Improvement

• Drive process improvement and regulatory intelligence initiatives
• Ensure audit readiness and compliance with internal quality systems

Requirements

• Degree in a life sciences discipline; advanced degree preferred
• Minimum of 6 years’ experience in Pharmacovigilance or Global Drug Safety
• Strong experience in clinical safety is required
• Strong clinical safety and post‑marketing experience
• Demonstrated leadership and line management capability
• Proven project management experience, including governance and delivery ownership
• Experience with aggregate reporting and safety documentation
• Strong knowledge of ICH, GVP, and GCP
• Experience working with safety databases
• Confident communicator with strong analytical and problem‑solving skills
• Fluent English, written and spoken

Desirable

• German language skills
• Consultancy or multi‑client experience

Benefits

• Work remotely while contributing to a global life sciences consultancy .
• Lead quality operations that directly influence patient safety and regulatory compliance.
• Collaborate in a multicultural, inclusive, and innovative environment.
• Enjoy opportunities for career progression, professional development, and international exposure.
• Flexible Work Options : Remote working flexibility to support your lifestyle.
• Generous Time Off: Enjoy 5 weeks of holiday plus national holidays and 3 personal days to recharge.
• Home Office Support: Get support to create a productive home office setup.
• Bonuses: Benefit from an annual bonus program, spot bonuses, and employee-nominated recognition.

Arriello is an Equal Opportunity Employer. We are committed to creating a diverse, inclusive, and respectful workplace where all individuals are valued and treated with dignity. We encourage applicants from all backgrounds, including but not limited to race, colour, religion, gender, gender identity, sexual orientation, age, disability, national origin, or any other characteristic protected by law.

In line with our commitment, we provide reasonable accommodations to applicants with disabilities throughout the hiring process. If you require any accommodation, please contact us at [email protected] .