As a Study Nurse, MFA or Clinical Research Coordinator (CRC) at IQVIA, you will be part of a dedicated team that strives to improve patient care. You will have the opportunity to contribute your expertise in an international environment and actively participate in the development of innovative therapies.

Your tasks:

• Coordinate and organise clinical trials according to study protocols and GCP guidelines
• Maintain and document study data in CRFs and EDC systems
• Respond to queries
• Prepare and send samples and manage materials
• Collaborate with investigators, study monitors and interdisciplinary teams
• Assist with administrative tasks and study visits

Your profile:

• Completed medical training (e.g. as a health and nursing professional, MFA, MTA), degree in life sciences
• At least 2 years of experience in clinical research or comparable qualification
• Proficient in MS Office and experience with EDC systems
• Excellent German language skills in writing and speaking, good English language skills an advantage
• Organisational skills, teamwork and a high level of self-responsibility
• Empathetic dealing with patients and enthusiasm for working in a study environment

IQVIA is committed to integrity in our hiring process and maintains a zero-tolerance policy for candidate fraud.

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