Clinical Research Coordinator: Onsite Trials & Impact

UNKNOWN; Lufkin (TX); On-site; USD 52,000 - 78,000; Full time

Job summary

SiteBridge Research Inc. is seeking a Clinical Research Coordinator or Clinical Research Nurse Coordinator to support the PI across multiple ongoing studies in Lufkin, TX. This 100% onsite role involves ensuring ICH/GCP compliance, site efficiency, and timely study completion.

Ideal candidates have hands-on clinical research experience; Clinical Research Assistants are encouraged to apply. Qualifications include a life science bachelor’s degree and experience in cardiology is a plus.

Qualifications

• Requires Bachelor’s degree in a life science.
• Experience in clinical site/trials is required.
• Knowledge of FDA & ICH GCP regulations is essential.

Responsibilities

• Communicate with study participants regarding study objectives and procedures.
• Conduct questionnaire administration and monitor participant compliance.
• Oversee activities to ensure adherence to protocols and regulatory standards.
• Maintain study documentation including case report forms and regulatory files.
• Coordinate participant screening, informed consent, and intake assessments.
• Track enrollment and document progress for multiple studies.

Skills

Clinical trials

FDA & ICH GCP

Analytical mindset

Excellent communication

Detail oriented

Problem solving

Education

Bachelor’s degree in life science

Tools

MS Office

Job description

SiteBridge Research Inc. is seeking a Clinical Research Coordinator or Clinical Research Nurse Coordinator to support the PI across multiple ongoing studies in Lufkin, TX. This 100% onsite role involves ensuring ICH/GCP compliance, site efficiency, and timely study completion.

Ideal candidates have hands-on clinical research experience; Clinical Research Assistants are encouraged to apply. Qualifications include a life science bachelor’s degree and experience in cardiology is a plus.