Jobs in the Netherlands, in English.

Clinical Research Physician

On-site in Groningen GRQM·Added 1 month ago (last checked 19 Oct)

ICON plc

8 open roles

Our summary

Work mode
On-site, Groningen GRQM
Contract
Permanent
Languages
Dutch

Skills

This job advert was originally written in Dutch.

Requirements

What we're looking for

  • Work experience in a clinical setting as a physician or PA, or a recent graduate in one of these roles.

  • Valid BIG registration is required for physicians and PAs; unfortunately, candidates without registration cannot be considered.

  • Strong clinical assessment skills and a professional focus on patient safety and ethical research practices.

  • Ability to make independent decisions, work within a multidisciplinary team, and contribute to the quality of clinical studies.

  • Communicatively skilled and able to collaborate effectively with colleagues within the Site Study Team.

  • Excellent communication skills in Dutch and English

Nice to have

  • Interest in and/or experience with clinical drug research is a plus.

The role

Clinical Research Physician

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.

At ICON, our people make the difference! We are looking for a Medical Reviewer or PA who wants to play a role in drug research.

In this role, you will screen participants, monitor safety, and contribute to groundbreaking clinical studies.

Our 'Own It' culture is about collaboration, integrity, and responsibility - and you will be given the space to make independent decisions and truly make a difference.

Do you want to be part of a dynamic team shaping the future of drug development? Join us!

What you'll do

  • Assisting in the recruitment and screening of healthy participants and patients for clinical trials.

  • Providing medical support during the conduct of studies.

  • Being responsible for the safety and well-being of participants and patients during studies.

  • Contributing to the research from a medical perspective by reviewing study protocols and actively collaborating within the Site Study Team to ensure the quality and compliance of clinical studies.

  • Maintaining the level of skills required for the practice of clinical medicine

Requirements

What ICON can offer you:
Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our benefits examples include

  • Various annual leave entitlements
  • A range of health insurance offerings to suit you and your family's needs.
  • Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
  • Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being.
  • Life assurance
  • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.

Visit our careers site to read more about the benefits ICON offers.

At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles.

Are you a current ICON Employee? Please click here to apply

About ICON plc

ICON is a clinical research organisation (CRO) providing outsourced clinical development and commercialisation services to the pharmaceutical, biotechnology and medical device industries. The company describes itself as the world's leading clinical research organisation and operates at global scale, with employees in 119 locations across 53 countries.

Its services span clinical and scientific operations, decentralised clinical trials, early clinical and laboratory services, medical imaging, regulatory affairs, consulting, commercialisation, medical writing, biometrics and outcome measures. ICON works across sectors including pharmaceuticals, biotech, medical devices and government and public health, and across therapeutic areas such as oncology, cardiovascular, central nervous system, vaccines and rare and orphan diseases.

Industry
Clinical research
Headquarters
Dublin, Ireland
All open roles at ICON plc
WhatsApp
Assen
Utrecht

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