The Clinical Research Associate I (CRA 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 (CRA I) is responsible for assisting in the planning, execution, and monitoring of clinical trials to ensure compliance with regulatory requirements and study protocols.
This role may coordinate the data collection and operations of multiple concurrent clinical research studies under the guidelines of research protocols, The University of Texas at Austin, and regulatory agency policies.
A successful candidate will possess strong attention to detail; excellent interpersonal, verbal, and written communication skills; the ability to coordinate with subjects, team members, other departments, and external institutions.
Matching Summary
The Clinical Research Associate I (CRA I) is responsible for assisting in the planning, execution, and monitoring of clinical trials to ensure compliance with regulatory requirements and study protocols.
Skills & Requirements
Must-have
GCP and ICH guidelines
IRB applications and submissions
Data entry into REDCap
Participant recruitment and enrollment
Maintain organized records
Nice-to-have
Strong attention to detail
Excellent communication skills
Ability to multitask
Prioritize and complete projects
Key Requirements
Bachelor's degree in life sciences or related field