Clinical Research Associate
vor 2 Wochen
About the Role
IQVIA is seeking an experienced Clinical Research Associate to join our team in Germany. As a CRA, you will be responsible for conducting site selection, initiation, monitoring, and close-out visits.
Job Description:
The ideal candidate will have a university degree in life science or other scientific discipline, and minimum one year of on-site monitoring experience.
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 on study sites and client representatives.
Requirements:
- 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.
- Good command of German and English.
- Flexibility to business travel up to 60% of working time.
- Driver's license class B.
About You:
- You have excellent analytical and problem-solving skills.
- You are able to communicate complex information clearly and concisely.
- You have a strong understanding of clinical trials and their management.
What We Offer:
- A competitive salary of €70,000 per annum.
- A comprehensive benefits package including home-office, company car/car allowance, accident insurance, pension, and more.
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