Research Coordinator

Hendrick Health; Abilene (TX); On-site; USD 52,000 - 68,000; Full time

Job summary

Hendrick Health in Abilene, TX seeks a Research Coordinator to support and coordinate daily clinical trial activities, working with Principal Investigators, sponsors, and department leadership to ensure compliance with federal regulations and organizational policies.

The role emphasizes data integrity and accurate reporting, with data capture in multiple databases and strong emphasis on GCP and human subject protections.

Qualifications

• Bachelor's degree required.
• 1–2 years of professional work experience.
• GCP and HSP training via CITI within 90 days of hire.

Responsibilities

• Support and coordinate daily clinical trial activities.
• Collaborate with Principal Investigators, sponsors, and department managers.
• Ensure clinical research is performed per federal regulations and policies.
• Utilize multiple online databases to track data and generate reports.

Skills

Organizational skills

Data management

Regulatory compliance

Data analysis

Report generation

Database usage

Attention to detail

Analytical thinking

Education

Bachelor's degree

Physical or social science degree preferred

Job description

Job Summary

The Research Coordinator plays a critical role in the conduct and completion of clinical trials by supporting, facilitating, and coordinating daily clinical trial activities. The Research Coordinator works with Principal Investigators, clinical trial sponsors and the department manager to help ensure that clinical research and related activities are performed in accordance with federal regulations and organizational policies and procedures.

Job Summary

The Research Coordinator plays a critical role in the conduct and completion of clinical trials by supporting, facilitating, and coordinating daily clinical trial activities. The Research Coordinator works with Principal Investigators, clinical trial sponsors and the department manager to help ensure that clinical research and related activities are performed in accordance with federal regulations and organizational policies and procedures.

Job Requirements

Minimum Education

• Bachelor's degree required
• Degree in physical or social science or related field preferred

Minimum Work Experience

• 1-2 years of professional work experience

Required Licenses/Certifications

• Good Clinical Practice (GCP) and Training in Protection of Human Research Subjects (HSP) certification required through Collaborative Institutional Training Initiative (CITI) within 90 days of hire.

Required Skills, Knowledge, And Abilities

• Excellent organizational skills
• Utilization of multiple online databases
• Analytical thinking and attention to detail
• Ensure data completeness
• Comply with regulatory standards
• Analyze data
• Run reports
• Track patient survival data

Designated Driver

• No

OSHA Category

• 3- Minimal Risk