Contract Conditions:
- Start date: ASAP
- Location: Germany
- Initial Contract Length: 6-12 months
- FTE: Full time
- Language: English and German are essential
- Project: Oncology
Responsibilities:
- Conduct site initiation, routine monitoring, and close-out visits for clinical trials.
- Maintain accurate and up-to-date clinical trial documentation, including monitoring reports,
regulatory documents, and essential documents.
- Ensure that all study activities are conducted in accordance with applicable regulatory requirements and guidelines.
- Provide training and support to investigational site staff on study protocols, data collection, and regulatory compliance.
- Monitor and review clinical trial data for accuracy, completeness, and consistency.
- Work closely with data management teams to resolve data discrepancies and ensure data quality.
- Travel to investigational sites as needed to conduct monitoring visits and attend study-related meetings.
Requirements
- Strong (10+ years preferred) experience as CRA
- Experience (5+ years preferred) working with Oncology preferred but not essential.
-Thorough understanding of GCP, regulatory requirements, and clinical trial processes.
- Willingness to Travel around Germany.
If this role is of interest to you, please apply directly to learn more about the role. If not feel free to share with your network.
