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Senior Clinical Research Associate
2 weeks ago
Job Opportunity
Senior Clinical Research Associates play a pivotal role in our team, ensuring clinical trial sites adhere to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
Main Responsibilities:
- Monitor clinical trial sites to guarantee compliance with study protocols, regulatory demands, and GCP guidelines
- Conduct site visits to assess performance, resolve issues, and provide support for successful trial execution
- Collaborate with cross-functional teams to ensure timely and accurate data collection and reporting
- Offer training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct
- Foster effective relationships with site personnel and stakeholders to facilitate smooth trial operations
Key Requirements:
- Advanced degree in a relevant field such as life sciences, nursing, or medicine
- Substantial experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements
- Minimum of 12 months of independent monitoring experience
- Demonstrated ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills
- Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools
About the Role:
This position requires a skilled professional who can work independently and collaboratively to deliver high-quality results. If you have a passion for clinical research and excellent communication skills, we encourage you to apply.