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Clinical Research Coordinator / Study Nurse (m/w/d) - Oldenburg

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IQVIA

4d ago

  • Job
    Full-time
    Junior Level
  • Research & Development
    Healthcare
  • Oldenburg

AI generated summary

  • You should have 2+ years of relevant experience, knowledge of clinical trials, strong IT skills, excellent interpersonal abilities, and fluent German.
  • You will coordinate clinical studies, ensure patient well-being, manage study documentation, assist in patient recruitment, and collaborate with monitors on study-related issues.

Requirements

  • Mindestens zwei Jahre einschlägige Erfahrung; oder eine gleichwertige Kombination aus medizinischer Ausbildung, Schulung und Erfahrung
  • Kenntnisse über klinische Studien, kombiniert mit fundierten Kenntnissen der abteilungs-, protokoll- und studienspezifischen Arbeitsabläufe, Einverständniserklärungen und Studienplänen
  • Ausgeprägte IT-Kenntnisse, geübt im Umgang mit MS Windows und Office-Anwendungen wie Access, Outlook, Excel und Word
  • Ausgezeichnete zwischenmenschliche Fähigkeiten mit der Fähigkeit, effektive Arbeitsbeziehungen aufzubauen und zu pflegen
  • Sehr gute Deutschkenntnisse in Wort und Schrift

Responsibilities

  • Koordinierung klinischer Forschungsstudien und Aufrechterhaltung eines sicheren Studienumfelds gemäß den Gesundheits- und Sicherheitsrichtlinien unter der Leitung und Delegation des Principal Investigators
  • Sicherstellung des Wohlergehens der PatientInnen, Eingehen auf deren Belange bei gleichzeitiger Gewährleistung der höchsten Qualität
  • Betreuung der PatientInnen und Unterstützung des Personals bei administrativen Aufgaben
  • Pflege von Studienprotokollen, Fallberichtsformularen (CRFs), elektronischen Datenerfassungssystemen (EDC) und anderen Studiendokumenten auf dem neuesten Stand
  • Planung und Koordinierung der logistischen Aktivitäten für Studienverfahren gemäß dem Studienprotokoll
  • Durchführung der klinischen Vorbereitungen für die Studie, einschließlich der Beschriftung von Probenentnahmeröhrchen und -behältern, der Inventarisierung des erforderlichen Materials und der Einrichtung oder Behebung von Problemen mit der Ausrüstung und/oder der Studie
  • Dateneingabe, Überprüfung der Datenqualität und Beantwortung von Fragen
  • Unterstützung bei der Aufnahme von PatientInnen in die Studie durch Rekrutierung, Screening und Einweisung gemäß dem Studienprotokoll
  • Sammeln, Erfassen und Berichten klinischer Daten und Befunde in angemessener Weise in CRFs und Zusammenarbeit mit dem Prüfarzt über studienbezogene unerwünschte Ereignisse und schwerwiegende unerwünschte Ereignisse gemäß dem Studienprotokoll
  • Koordinierung mit dem Studienmonitor bei Studienproblemen und effektive Beantwortung der vom Monitor gestellten Fragen.

FAQs

What is the employment type for this position?

This is a part-time position, requiring 24 hours per week.

How long is the duration of the employment?

The position is available for approximately 3 months.

When is the start date for this role?

The position is available for immediate start.

What are the main responsibilities of the Clinical Research Coordinator/Study Nurse?

Main responsibilities include coordinating clinical research studies, ensuring patient well-being, supporting staff with administrative tasks, maintaining study documents, planning logistical activities, conducting clinical preparations for the study, and data entry and management.

What qualifications are required for this position?

Candidates should have at least two years of relevant experience or an equivalent combination of medical education, training, and experience.

Are there specific knowledge or skills required for this role?

Yes, knowledge of clinical studies, proficiency in MS Windows and Office applications, excellent interpersonal skills, and very good German language skills are required.

Do I need prior experience in clinical research to apply?

Yes, at least two years of relevant experience is required for this role.

Is there a requirement for understanding study protocols and consent forms?

Yes, candidates must have a solid understanding of department, protocol, and study-specific workflows, including informed consent and study plans.

Are there opportunities for career growth in this position?

Yes, working with IQVIA can provide further opportunities in the field of clinical research and healthcare.

Will I be working directly with patients?

Yes, the role involves patient care, including their recruitment, screening, and ensuring their well-being throughout the study.

What languages should I be proficient in for this position?

Very good German language skills, both spoken and written, are required for this role.

Can I apply for this position if I do not have IT skills?

No, strong IT skills, particularly with MS Office applications, are essential for this position.

Is this position suitable for someone looking to start a career in clinical research?

While relevant experience is required, this position can be a valuable opportunity for those aiming to advance their career in clinical research.

Accelerate innovation for a healthier world.

Science & Healthcare
Industry
10,001+
Employees

Mission & Purpose

IQVIA (NYSE:IQV) is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. IQVIA creates intelligent connections across all aspects of healthcare through its analytics, transformative technology, big data resources and extensive domain expertise. IQVIA Connected Intelligence™ delivers powerful insights with speed and agility — enabling customers to accelerate the clinical development and commercialization of innovative medical treatments that improve healthcare outcomes for patients. With approximately 86,000 employees, IQVIA conducts operations in more than 100 countries. IQVIA is a global leader in protecting individual patient privacy. The company uses a wide variety of privacy-enhancing technologies and safeguards to protect individual privacy while generating and analyzing information on a scale that helps healthcare stakeholders identify disease patterns and correlate with the precise treatment path and therapy needed for better outcomes. IQVIA’s insights and execution capabilities help biotech, medical device and pharmaceutical companies, medical researchers, government agencies, payers and other healthcare stakeholders tap into a deeper understanding of diseases, human behaviors and scientific advances, in an effort to advance their path toward cures.

Benefits

  • Medical, dental and vision coverage

  • Employee Assistance Programs

  • Mental health support

  • Flexible work environment

  • Time off for leisure, personal time and corporate holidays

  • Parental leave for birth or adoption

  • Paid leave for other life matters (i.e., illness, bereavement, jury duty, military service, etc.)

  • Retirement and savings plans

  • Commuter benefits