Description
We are seeking a Study Nurse, MFA or Clinical Research Coordinator to join our team in Berlin Mitte on a part-time basis (24 hours/week) for a fixed term of 1 year.
As a Study Nurse, MFA or Clinical Research Coordinator, you will play a crucial role in coordinating and organizing clinical trials in accordance with study protocols and GCP guidelines.
Responsibilities:
- Coordinate and organize clinical studies according to study protocols and GCP guidelines
- Provide care and support to study patients throughout the study duration
- Maintain and document study data in CRFs and EDC systems
- Prepare and send samples, as well as manage materials
- Collaborate with investigators, study monitors, and interdisciplinary teams
- Assist with administrative tasks and study visits
Requirements:
- Completed medical training (e.g., as a health and nursing professional, MFA, MTA), or a degree in life sciences
- At least 2 years of experience in clinical research or comparable qualification
- Oncology experience is an advantage
- Proficiency in MS Office and experience with EDC systems
- Excellent German language skills in writing and speaking, good English skills beneficial
- Organizational skills, teamwork, and a high level of self-responsibility
- Empathetic approach to patients and enthusiasm for working in a study environment
Benefits:
- Opportunity to work in an international environment
- Collaborative and supportive team
IQVIA is committed to integrity in our hiring process and maintains a zero-tolerance policy for candidate fraud.