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Pharmacovigilance Scientist [F/M/X]

๐Ÿ“ Amsterdam, nl

Technologie Amaris Consulting

Functiebeschrijving

Who are we?

Lees de onderstaande informatie voor meer informatie over deze functie en solliciteer vervolgens om in aanmerking te komen.

Amaris Consulting

is an independent technology consulting firm providing guidance and solutions to businesses. With more than 1,000 clients across the globe, we have been rolling out solutions in major projects for over a decade โ€“ this is made possible by an international team of 7,600 people spread across 5 continents and more than 60 countries. Our solutions focus on four different Business Lines: Information System & Digital, Telecom, Life Sciences and Engineering. Weโ€™re focused on building and nurturing a top talent community where all our team members can achieve their full potential. Amaris is your steppingstone to cross rivers of change, meet challenges and achieve all your projects with success.

At Amaris, we strive to provide our candidates with the best possible recruitment experience. We like to get to know our candidates, challenge them, and be able to give them proper feedback as quickly as possible. Here's what our recruitment process looks like:

Brief Call : Our process typically begins with a brief virtual/phone conversation to get to know you! The objective? Learn about you, understand your motivations, and make sure we have the right job for you!

Interviews

(the average number of interviews is 3 - the number may vary depending on the level of seniority required for the position). During the interviews, you will meet people from our team: your line manager of course, but also other people related to your future role. We will talk in depth about you, your experience, and skills, but also about the position and what will be expected of you. Of course, you will also get to know Amaris: our culture, our roots, our teams, and your career opportunities!

Case study : Depending on the position, we may ask you to take a test. This could be a role play, a technical assessment, a problem-solving scenario, etc.

As you know, every person is different and so is every role in a company. That is why we have to adapt accordingly, and the process may differ slightly at times. However, please know that we always put ourselves in the candidate's shoes to ensure they have the best possible experience.

We look forward to meeting you!

Job Description

Are you passionate about patient safety and making a real impact in the pharmaceutical industry? Amaris Consulting is supporting a leading global pharmaceutical company in their mission to ensure drug safety and regulatory excellence. We are seeking a detail-oriented and proactive

Pharmacovigilance Scientist

to join their dynamic Global Pharmacovigilance team based in

Amsterdam .

This is a full-time opportunity to work at the heart of pharmacovigilance operations, contributing directly to the safety monitoring of innovative medicines used by patients worldwide.

Your Role โ€“ What Youโ€™ll Do:

Process Individual Case Safety Reports (ICSRs) from global sources: assess validity, code using MedDRA, conduct follow-up, and ensure timely submissions to regulatory authorities. Maintain and manage data in the safety database with high accuracy and compliance. Support the preparation of key safety documents, including Periodic Benefit-Risk Evaluation Reports (PBRER) and Development Safety Update Reports (DSUR). Contribute to signal detection and risk management activities by analyzing safety data trends. Ensure full compliance with Good Pharmacovigilance Practices (GVP), SOPs, and KPIs. Collaborate effectively with internal teams and external partners, including CROs, to ensure seamless safety operations. Participate in audits, inspections, and continuous improvement initiatives.

What You Bring โ€“ Your Profile:

Bachelorโ€™s degree (or higher) in a medical, pharmaceutical, or life sciences field. Minimum of 2 years of hands-on experience in pharmacovigilance or drug safety. Solid understanding of ICSR processing, GVP guidelines, and global regulatory requirements. Experience with safety databases (e.g., ARISg, Argus, or similar) and MedDRA coding. Strong analytical mindset with excellent attention to detail. Fluent in English (written and spoken). Proficiency in Dutch is a plus, but not required. Proactive, independent, and able to thrive in a fast-paced, collaborative environment.

Why Join?

Be part of a global team dedicated to patient safety and innovation. Work with cutting-edge systems and processes in a GMP- and GVP-compliant environment. Grow your career with support for professional development and training. Flexible working options and a supportive, inclusive culture.

Ready to make an impact?

Apply today and become a key player in safeguarding patient health worldwide.

Amaris Consulting is proud to be an equal opportunity workplace. We are committed to promoting diversity within the workforce and creating an inclusive working environment. xjpvoyz For this reason, we welcome applications from all qualified candidates, regardless of gender, sexual orientation, race, ethnicity, beliefs, age, marital status, disability, or other characteristics.

Ready to Apply?

Don't miss this opportunity! Apply now and join our team.

Functiedetails

Publicatiedatum: December 16, 2025
Functietype: Technologie
Locatie: Amsterdam, nl
Company: Amaris Consulting

Ready to Apply?

Don't miss this opportunity! Apply now and join our team.