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Medical Reviewer for Clinical Data

Posted 27 days ago

OfficeAmsterdam, North Holland, Netherlands

Join Excelya, where Audacity, Care, and Energy define who we are and how we work. We believe in creating bold solutions and fostering an inclusive environment where collaboration and individual growth go hand in hand.  

 

This role is an exciting opportunity to contribute to a dynamic, ambitious team in Medical Affairs. You will play a critical part in driving innovation and making an impact in the clinical research space, while enjoying a stimulating professional environment that encourages personal and intellectual growth. 

 

The Study Medical Reviewer is accountable for managing/reviewing the medical consistency of reported clinical data to ensure that medical data in database are accurate, reliable and analyzable. He/Her has the responsibility of his/her studies/projects to provide reliable and consistent data from a medical point of view and to bring medical expertise to all processes from the set-up to the lock of the study.

Main Responsibilities

  • Oversee the medical review process
  • Ensure the reliability of medical data reported in the clinical trials under his/her responsibilities
  • Seriousness review of adverse events
  • Contribute in all processes from the initiation to the completion of clinical trials, thanks to his/her medical expertise
  • Actively participate in Study Team activities as the representative for medical review activities.

Requirements

At Excelya, taking audacious steps is encouraged, so we’re looking for individuals who are ready to grow with us and share our values.  

 

• Experience: medical review, oncology, clinical development, medical expert

• Skills: ability to work across functions, curiosity, ability to handle large amounts of data, strong organizational skills, ability to prioritize, English

• Previous professional experience: Doctors, pharmacists, PhD with experience in medical review), coming from industry sector.

• Languages: Fluency in French and English

Nice to have experience in coding, knowledge of Who Drug and MedDRA dictionaries*

Benefits

Why Join Us?

At Excelya, we combine passion for science with enthusiasm for teamwork to redefine excellence in healthcare.

Here’s what makes us unique.

We are a young, ambitious health company representing 900 Excelyates, driven to become Europe’s leading mid-size CRO with the best employee experience. Our one-stop provider service model - offering full service, functional service provider, and consulting - enables you to evolve through diverse projects. Working alongside preeminent experts, you will help improve scientific, operational, and human knowledge to enhance the patient's journey.

 

Hiring Manager’s Note

“Come and join a nice working environment with a good balance between professional and personal work, a company where with supportive easy colleagues to work with”

Excelling with Care

At Excelya, Care lies at the heart of what we do. We provide equal opportunities for all and foster a diverse, equitable, and inclusive workplace where humility and boldness work hand in hand. Everyone has a space to feel valued, thrive, and collaborate with purpose.

Your challenges become our shared mission. Together, we transform bold ideas into reality, the Excelya way.

Watch our testimonial video to hear directly from our Excelyates about why Excelya is more than just a workplace—it’s a community built on values.

Apply today, become an Excelyate!

Job details
Workplace
Office
Location
Amsterdam, North Holland, Netherlands

Excelya is an independent, Paris-headquartered contract research organization (CRO) founded in 2014 that supports biotech, pharmaceutical, and medical device companies with full-service CRO, FSP, and resourcing solutions across clinical development. The company operates through a global network with 900+ experts and coverage in 25 countries, offering capabilities in areas such as clinical operations, data management, biometrics, pharmacovigilance, regulatory affairs, and medical affairs to help clients deliver clinical trials and bring new therapies to patients.

Key team members

Julien Sallaind

Julien Sallaind

Elitza Ouzounova

Elitza Ouzounova

Emilie Stefanelli

Emilie Stefanelli

Laurence MAUNIER

Laurence MAUNIER

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