
Senior Clinical Research Associate
6 days ago
A clinical research associate (CRA) is responsible for ensuring that clinical trials are conducted according to established standards and protocols. As a CRA, you will conduct on-site and remote monitoring of clinical research studies to ensure compliance with widely accepted clinical practices.
This includes developing and implementing tools, procedures, and processes to ensure quality monitoring. You will also contribute to the design, implementation, and delivery of processes, programs, and policies related to clinical monitoring, ensuring alignment with organizational goals.
Key responsibilities include:
- Conducting comprehensive on-site and remote monitoring of clinical research studies
- Developing and implementing tools, procedures, and processes to ensure quality monitoring
- Assisting in the design, implementation, and delivery of processes, programs, and policies related to clinical monitoring
- Collaborating with study teams to ensure accurate and timely data collection, entry, and reporting
Required Skills and Qualifications
To be successful in this role, you will need:
- Bachelor's degree in a relevant field such as life sciences, nursing, or a related discipline
- Previous experience in clinical research or a related field
- Strong understanding of clinical trial processes and regulations
- Excellent organizational and time management skills
Benefits
We offer a competitive compensation package, including benefits such as medical, dental, and vision insurance, 401(k) matching, and paid time off. We also provide opportunities for professional growth and development, including training and mentoring programs.
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