Clinical Monitoring Specialist
2 semanas atrás
The primary objective of this position is to perform and coordinate assigned aspects of the clinical monitoring process in accordance with regulatory requirements.
This entails conducting site visits to determine protocol compliance, preparing required documentation, developing collaborative relationships with investigative sites, and providing study training.
A strong understanding of clinical trial processes, excellent communication skills, and the ability to prioritize tasks are essential for success in this role.
- Monitor and coordinate clinical trials at designated sites to ensure adherence to protocol requirements.
- Develop and maintain effective working relationships with cross-functional teams, including study vendors and investigative sites.
Minimum Requirements:
- Bachelor's degree in a relevant scientific discipline.
- At least 2+ years of experience in clinical operations, with a minimum of 1+ year in monitoring.
Key Competencies:
- Teamwork and collaboration
- Honest and actionable feedback
- Self-awareness and adaptability
- Inclusive behavior and continuous learning
- Results-oriented and analytical thinking
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