Clinical Research Associate I - Study Coordination

University of Texas; Austin (TX); On-site; USD 60,000 - 80,000; Full time

Job summary

A premier academic institution in Austin is seeking a Clinical Research Coordinator to oversee various aspects of clinical trials. The ideal candidate will ensure compliance with protocols, manage site performance, and coordinate participant schedules. A Bachelor's degree in life sciences or nursing and relevant experience in clinical research are required. Candidates should demonstrate strong analytical and collaboration skills. This role offers a dynamic work environment and the chance to contribute to significant research initiatives.

Qualifications

• 1 year of relevant clinical research experience.
• 2 years of experience in clinical research for Master's holders.
• Good Clinical Practice (GCP) Certification required.

Responsibilities

• Conducts site initiation, monitoring, and close-out visits.
• Ensures compliance with study protocols and regulatory requirements.
• Manages site performance and resolves issues.

Skills

Basic proficiency in Microsoft Office Suite (Word, Excel, Outlook)

Ability to analyze information and develop solutions

Detail-oriented with strong time management

Effective collaboration with participants and research teams

Education

Bachelor's Degree in life sciences, nursing, or a related field

Master's Degree in life sciences, nursing, or a related field

Tools

REDCap

Job description

A premier academic institution in Austin is seeking a Clinical Research Coordinator to oversee various aspects of clinical trials. The ideal candidate will ensure compliance with protocols, manage site performance, and coordinate participant schedules. A Bachelor's degree in life sciences or nursing and relevant experience in clinical research are required. Candidates should demonstrate strong analytical and collaboration skills. This role offers a dynamic work environment and the chance to contribute to significant research initiatives.