Base: $40,000 + depending on qualifications; bonus...
Bachelor's degree in life sciences or nursing
1 year clinical research experience
Good clinical practice (gcp) guidelines adherence
The Clinical Research Associate I is responsible for assisting in the planning, execution, and monitoring of clinical trials to ensure compliance with regulatory requirements and study protocols
Job Summary
The Clinical Research Associate I is responsible for assisting in the planning, execution, and monitoring of clinical trials to ensure compliance with regulatory requirements and study protocols.
Key duties include conducting site initiation visits, managing participant recruitment and retention, and ensuring accurate data entry into electronic systems.
This grant-funded position offers a salary range starting at $40,000 depending on qualifications and requires adherence to GCP and FDA regulations.
Matching Summary
The Clinical Research Associate I is responsible for assisting in the planning, execution, and monitoring of clinical trials to ensure compliance with regulatory requirements and study protocols.
Salary
Base: $40,000+ depending on qualifications; Bonus/Equity: Not specified; Benefits: Teacher Retirement System (TRS) eligible
Skills & Requirements
Must-have
Bachelor's degree in life sciences or nursing
1 year clinical research experience
Good Clinical Practice (GCP) guidelines adherence
Electronic data capture system proficiency
IRB application and submission support
Nice-to-have
Master's degree in related field
2 years of clinical research experience
Certified Clinical Research Associate credential
CITI Human Subjects Research Training
Experience with REDCap platform
Key Requirements
Bachelor's Degree in life sciences, nursing, or related field
1 year of relevant clinical research experience
Good Clinical Practice (GCP) Certification preferred