Clinical Resarch Nurse - Malmö

IQVIA · Gothenburg, Sverige · part time · På plats · 4 februari 2026

Registrera dig för att söka
Ditt första är gratis
Publicerad 4 februari 2026 · Inläst från IQVIA
Varför ett CV för det här jobbet?

94% av arbetsgivarna säger att deras filter sållar bort kvalificerade kandidater vars CV inte matchar annonsens exakta kriterier (Harvard Business School, 2021).

  • De ser det de bad om, först. Den erfarenhet som matchar annonsen kommer först, med annonsens egna ord, så att den som skummar hittar det på några sekunder.
  • Det tar sig förbi programvaran. Många större arbetsgivare använder program som rangordnar CV:n efter hur väl de matchar annonsen, ofta innan någon har läst dem.
  • På annonsens språk. En annons skriven på engelska får ett CV på engelska, även när ditt är på svenska.
  • Dina fakta, inget påhittat. Din egen erfarenhet, omordnad och omformulerad. Det annonsen vill ha och ditt CV inte visar listas så att du kan lägga till det, bara om det stämmer. Du kontrollerar det innan du skickar det.
Se ett exempel

Clinical Research Nurse - Malmö, part time 24h per week

Start Date: Immediate

Duration: Approximately 6 months

IQVIA is currently recruiting a dedicated Clinical Research Nurse to support a clinical research site in Malmö. This part-time position offers a unique opportunity to contribute to meaningful research in a collaborative and dynamic environment.

Key Responsibilities

As a vital member of the site team, you will help ensure the smooth execution of the clinical trial by performing a range of administrative and clinical support tasks, including:

  • Maintaining and updating study documentation, including protocols, case report forms (CRFs), and Electronic Data Capture (EDC) systems
  • Take and record vital signs (incl. weight, height), perform ECG
  • Supporting patient screening and enrollment, including handling informed consent and privacy documentation
  • Investigational Product (IP): Manage receipt and storage, perform accountability and compliance, prepare, dispense and administer IP
  • Coordinating logistical activities for study procedures in line with the study protocol
  • Performing data entry, quality checks, and resolving queries to ensure data accuracy and completeness
  • Managing and shipping biological samples
  • Communicating with study monitors and responding to study-related inquiries
  • Carrying out general administrative tasks related to the study

Your Profile

We are looking for candidates who bring a combination of education, experience, and skills:

  • Current RN registration
  • Solid understanding of clinical trials and familiarity with study protocols, consent forms, and schedules
  • good knowledge of medical terminology
  • Strong IT skills, including proficiency in MS Office applications (Outlook, Word, Excel, Access)
  • Must have at least 1-2 years experience working as a Research Nurse at a clinical trial site
  • Experience in collecting patient vital signs and laboratory samples, administering investigational products, and conducting electrocardiograms (EKGs) is considered an advantage
  • Excellent interpersonal and communication skills
  • Strong organizational skills and attention to detail

Why Join IQVIA?

At IQVIA, you will be part of a global team that is advancing healthcare through data, technology, and human science. We offer a supportive work environment, impactful projects, and the opportunity to make a real difference.

Interested?

If this sounds like the right opportunity for you, we encourage you to apply today.

#LI-HCPN

#LI-CES

#LI-DNP

#LI-Onsite

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Arbetsgivare
IQVIA
Ort
Gothenburg, Sverige · På plats
Anställningsform
part time