Hiring.Camp

Clinical Research Physician

Icon

·

6 days ago

Location
Netherlands, Groningen GRQM
Workplace
Onsite
Type
Full-time
Department
Healthcare
Visa
Not sponsored
Source
Workday

Description

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.


Bij ICON maken onze mensen het verschil! We zoeken een keuringsarts of PA die graag een rol wil spelen in geneesmiddelenonderzoek.

In deze rol screen je deelnemers, bewaak je de veiligheid en draag je bij aan baanbrekende klinische studies.

Onze ‘Own It’-cultuur draait om samenwerking, integriteit en verantwoordelijkheid – en jij krijgt de ruimte om zelfstandig beslissingen te nemen en echt verschil te maken.

Wil jij deel uitmaken van een dynamisch team dat de toekomst van geneesmiddelenontwikkeling vormgeeft? Sluit je bij ons aan!

De rol van Keuringsarts / Physician Assistant:

  • Helpen bij het werven en screenen van gezonde deelnemers en patiënten voor klinische onderzoeken.

  • Medische ondersteuning bieden bij het uitvoeren van onderzoeken.

  • Verantwoordelijk zijn voor de veiligheid en het welzijn van deelnemers en patiënten tijdens onderzoeken.

  • Bijdragen aan het onderzoek vanuit medisch perspectief door het reviewen van onderzoeksprotocollen en het actief meewerken binnen het Site Study Team om de kwaliteit en naleving van klinische studies te waarborgen.

  • Het niveau van vaardigheden behouden dat nodig is voor de praktijk van klinische geneeskunde

Vereisten

  • Werkervaring in een klinische omgeving als arts of PA of recent afgestudeerd in een van deze functies.

  • Geldige BIG-registratie is vereist voor artsen en PA’s; kandidaten zonder registratie kunnen helaas niet worden overwogen.

  • Sterke klinische beoordelingsvaardigheden en een professionele focus op patiëntveiligheid en ethische onderzoekspraktijken.

  • Interesse in en/of ervaring met klinisch geneesmiddelenonderzoek is een pré.

  • Vermogen om zelfstandig beslissingen te nemen, binnen een multidisciplinair team te werken en bij te dragen aan de kwaliteit van klinische studies.

  • Communicatief vaardig en in staat om effectief samen te werken met collega’s binnen het Site Study Team.

  • Uitstekende communicatie vaardigheid in Nederlands en Engels

#LI-CL1


Employment with ICON is contingent upon having the legal right to work in the country where the role is based.


Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.


Benefits may include:

  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.


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


Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.


If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.

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

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