Clinical Monitor at University Hospital Muenster
Berlin, Berlin, Germany -
Full Time


Start Date

Immediate

Expiry Date

18 Nov, 26

Salary

0.0

Posted On

20 Aug, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Industry

Hospitals & Health Systems

Description

About this job

Reference number: 12377

Fixed-term contract for 2 years with possibility of extension | Full-time | 38.5 hours per week | Salary according to TV-L (Collective Agreement for Public Service Employees in the German States) | Center for Clinical Studies (ZKS) Münster

We are UKM. We have a clear social mission and a special responsibility in combining patient care, research and teaching.

To ensure we meet our high standards every day, we look forward to your professional expertise at the Center for Clinical Studies (ZKS) Münster. The ZKS supports clinical research projects with its many years of experience and contributes to ensuring high-quality clinical research at the University Hospital Münster (UKM). Together, we will shape the medical research of tomorrow – ideally with you!

RESPONSIBLE TASKS:

  • Implementation of monitoring of clinical research projects within the framework of quality assurance
  • Independent planning, organization and execution of initiation, monitoring and conclusion visits
  • Support and guidance for the participating testing centers during the study implementation
  • Initiation of new testing facilities including preparation and documentation
  • Ensuring compliance with legal, regulatory and study-specific requirements
  • Documentation of monitoring activities and follow-up of agreed measures

REQUIREMENTS:

  • Experience in clinical trial monitoring or study assistance is desirable.
  • Alternatively, a completed degree in natural sciences or completed medical vocational training (e.g., medical assistant or medical technical assistant) with knowledge of clinical trials, for example through a CRA course.
  • Sound knowledge of national and international regulations for clinical trials (GCP)
  • Experience in quality and risk management
  • Good English skills, both spoken and written.
  • Independent, structured and reliable work ethic as well as organizational skills
  • Strong communication skills, teamwork skills and assertiveness
  • Willingness to undertake regular business trips and interest in clinical research

WE OFFER:

  • Remuneration according to TV-L, annual bonus payment and company pension scheme (VBL)
  • 30 days of vacation per year plus two extra days off on Christmas Eve and New Year's Eve
  • Diverse training and further education opportunities for your development
  • Respectful interaction and appreciative collaboration in a diverse team
  • Numerous support and advice services on the topics of health or reconciling family and career.
  • Many other benefits such as company bike scheme, sports offers, job ticket, company parties, canteen or childcare in emergencies


For further information, please contact: Thorsten Northoff, Managing Director, T 0251 83-57110
Responsibilities
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