Clinical Research Associate
vor 3 Wochen
As a Clinical Research Associate at IQVIA, you will play a critical role in the success of our clients' clinical trials. Your responsibilities will include performing site selection, initiation, monitoring, and close-out visits, as well as supporting the development of a subject recruitment plan.
Key Responsibilities:
- Perform site selection, initiation, monitoring, and close-out visits
- Support the development of a subject recruitment plan
- Evaluate the quality and integrity of site practices in accordance with regulatory requirements
- Manage progress by tracking regulatory submissions, recruitment, case report form completion, and data query resolution
- Collaborate with experts at study sites and with client representatives
Qualifications:
- University Degree in life science or other scientific discipline
- Minimum of one year of on-site monitoring experience
- Knowledge of applicable clinical research regulatory requirements
- Strong written and verbal communication skills, attention to detail, and ability to work in a fast-paced environment
- Fluency in German on at least C1 level and a good command of English
- Flexibility to travel up to 40-60% of working time
About IQVIA:
IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world.
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