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Global Drug Safety Manager

Roles & Responsibilities

  • Degree in a life sciences discipline; advanced degree preferred
  • Minimum of 6 years’ experience in Pharmacovigilance or Global Drug Safety
  • In-depth knowledge of Global Drug Safety regulations including ICH, GVP and GCP
  • Proven experience in aggregate reporting and safety documentation

Requirements:

  • Lead delivery of Global Drug Safety projects ensuring quality, compliance and client satisfaction
  • Provide line management and oversight of team members, including mentoring and training
  • Act as Project Manager and ensure delivery to timelines and client expectations
  • Oversee safety data management, signal management and benefit-risk activities

Job description

This is a remote position.

About Arriello:

 

At Arriello, we provide a full range of   Pharmacovigilance, Quality & Compliance, and Regulatory Affairs  services to global pharmaceutical and life sciences companies. With a team of experienced professionals, we support our clients in meeting their regulatory obligations, maintaining product quality and patient safety, and navigating complex global compliance landscapes.

 

As a growing business with a dynamic culture, we are committed to  high-quality delivery, continuous improvement, and creating an environment where people can thrive.

 

At Arriello, our values define how we work — and who we are:

Inclusive -    We value equity, inclusion and dignity for all, recognising that we learn from each other every day.

Dedicated -    We challenge the status quo to deliver pragmatic, tailored solutions for our clients.

Innovative -    We collaborate closely—with our clients, colleagues and partners—to proactively find better ways forward.

Passionate -    We build strong relationships based on empathy, respect and a genuine commitment to delivering quality in everything we do.



The opportunity
This is a fully remote role, supporting ongoing portfolio growth and project demand as part of a 12 Month Fixed-Term Contract.

You will join a structured and experienced Global Drug Safety team, playing a key role in both technical delivery and people management across multiple client projects. This is a senior position suited to an experienced pharmacovigilance professional who can lead teams, manage complex projects and drive high quality delivery in a global, remote environment.


What you will do


Main Purpose of the Role
You will lead technical delivery within Global Drug Safety projects while providing line management and guidance to team members. You will oversee project execution, ensure high quality outputs, and support continuous improvement across systems, processes and service delivery.


Key Responsibilities

  • Lead delivery of Global Drug Safety projects, ensuring quality and compliance
  • Provide line management and oversight of team members
  • Act as Project Manager and ensure delivery to timelines and client expectations
  • Support and oversee aggregate reporting, safety documentation and medical writing activities
  • Provide technical guidance, mentoring and training across the team
  • Support business development activities including proposals and client interactions
  • Oversee safety data management, signal management and benefit risk activities
  • Support regulatory intelligence and process improvement initiatives
  • Ensure audit readiness and compliance with internal systems and procedures


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
  • In depth knowledge of Global Drug Safety regulations including ICH, GVP and GCP
  • Proven experience in aggregate reporting and safety documentation
  • Previous experience in team leadership and project management
  • Experience working with safety databases
  • Strong communication, organisational and stakeholder management skills
  • Fluent English, written and spoken
  • German language skills are an advantage


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    recruitment@arriello.com   .

 



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