Clinical Research Associate
vor 4 Wochen
We are a research-driven biopharmaceutical company dedicated to inventing medicines and vaccine innovations that make a significant impact on global healthcare. Our Clinical Research and Pharmacovigilance team ensures the safety and efficacy of our products through clinical trials and surveillance.
As a Clinical Research Associate, you will be responsible for ensuring compliance with ICH/GCP and country regulations, company policies, and quality standards. You will act as the primary point of contact for study sites and site managers, taking overall responsibility for allocated sites.
Key Responsibilities:
- Primary site contact and responsible for site management and monitoring activities throughout all study phases.
- Assisting allocated sites with open matters and requests.
- Collection of regulatory documents and management of data in clinical trial systems.
- Ensuring study conduct is in compliance with relevant regulations and standards.
- Serving as a subject matter expert for monitoring processes and systems.
Requirements:
- Previous experience working as a Clinical Research Associate.
- High level of personal responsibility and ability to support site staff on-site.
- Strong communication and presentation skills.
- Flexibility and ability to support sites in a changing environment.
- Excellent verbal and written communication skills in English and German.
We Offer:
An attractive salary, outstanding social benefits, and an exciting work environment with varied tasks in an international environment.
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