Clinical Resarch Nurse - Malmö

IQVIA LLC; Göteborgs kommun; On-site; SEK 30,000 - 40,000; Part time

Job summary

A global clinical research company seeks a dedicated Clinical Research Nurse to join their team in Gothenburg for a part-time role of 24 hours per week. The ideal candidate will have RN registration and 1-2 years of experience in clinical trials. Responsibilities include maintaining study documentation, managing vital signs and ECGs, and coordinating patient enrollments. This position offers the chance to contribute to impactful research in a collaborative environment.

Qualifications

• 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 is an advantage.
• Ability to perform ECG and manage investigative products.

Responsibilities

• Maintain and update study documentation.
• Take and record vital signs, and perform ECG.
• Support patient screening and enrollments.

Skills

Current RN registration

Understanding of clinical trials

Good knowledge of medical terminology

Strong IT skills (MS Office)

Interpersonal and communication skills

Organizational skills

Job description

Clinical Resarch Nurse - Malmö page is loaded## Clinical Resarch Nurse - Malmölocations: Gothenburg, Swedentime type: Part timeposted on: Posted Todayjob requisition id: R1527127**Clinical Research Nurse - Malmö, part time 24h per week****Start Date**: Immediate **Duration**: Approximately 6 monthsIQVIA 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 detailAt 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.If this sounds like the right opportunity for you, we encourage you to apply today.#LI-HCPN#LI-CES#LI-DNP#LI-OnsiteIQVIA 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 atIQVIA 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.IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.