Industry Pharma/Biotech/Clinical Research
Remote Job
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
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 ****** .
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