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Clinical Oncology Coordinator
2 semanas atrás
As a key member of our clinical operations team, you will be responsible for conducting site visits to ensure compliance with protocols and regulations. You will build strong relationships with site personnel and facilitate effective communication.
The ideal candidate will have a degree in a relevant scientific discipline and at least 2 years of experience in clinical operations. Prior monitoring experience is also essential. Experience in global oncology trials is highly desirable.
- Main Responsibilities:
- Perform assigned aspects of the clinical monitoring process in accordance with GCPs and SOPs.
- Conduct site visits to determine protocol and regulatory compliance and prepare required documentation.
- Develop collaborative relationships with investigative sites and study vendors.
- Provide protocol and related study training to assigned clinical study sites.
- Maintain oversight of site performance by tracking metrics for enrollment, data entry into Case Report Forms (CRFs), protocol deviation trends, and overall site issues.
- Serve as mentor/trainer for less experienced CRAs to assist with general and study-specific monitoring issues.
- Key Skills:
- Fosters Teamwork
- Provides and Solicits Honest and Actionable Feedback
- Self-Awareness
- Acts Inclusively
- Demonstrates Initiative
- Entrepreneurial Mindset
- Continuous Learning
- Embraces Change
- Results-Oriented
- Analytical Thinking/Data Analysis
- Financial Excellence
- Communicates with Clarity
We offer a dynamic and supportive work environment that promotes professional growth and development.