Description
Join IQVIA as an Experienced CRA in our Clinical Site Management department, working from home throughout Germany. You will focus on comprehensive clinical trial management in various indications and learn about the diverse scientific approaches of sponsors. You will establish strong relationships with the global study team and involved investigators, conduct monitoring on complex clinical trials for different pharma companies, and ensure adherence to good clinical practices and study protocols.
Your responsibilities will include:
- Performing site selection, initiation, monitoring, and close-out visits
- Supporting the development of a subject recruitment plan
- Evaluating the quality and integrity of site practices in accordance with regulatory requirements, such as Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
- Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution
- Collaborating with experts on study sites and client representatives
Qualifications:
- University degree in life science or other scientific discipline, or apprenticeship in healthcare
- Minimum of one year of on-site monitoring experience, or alternatively, minimum one year of experience as Study Coordinator/CTC, etc.
- Knowledge of applicable clinical research regulatory requirements, such as Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
- Strong written and verbal communication skills, attention to detail, and ability to work in a fast-paced environment
- Fluent command of German and English
- Flexibility to business travel up to 60% of working time
- Driver's license class B
What you can expect:
- Resources that promote your career growth
- Leaders that support flexible work schedules
- Programs to help you build your therapeutic knowledge
- Dynamic work environments that expose you to new experiences
- Home-office, company car/car allowance, accident insurance, pension, and more