Clinical Research Coordinator — 6-Month Contract, Lufkin

Experis Austria; Lufkin (TX); On-site; USD 36,000 - 44,000; Full time

Benefits offered by this job

Medical plan

Dental plan

Vision plan

HSA

FSA

Dependent care FSA

Life insurance

Disability insurance

Travel insurance

401(k) match

Weekly pay

Job summary

Experis Austria seeks a Clinical Research Coordinator to join a leading healthcare and clinical research organization in Lufkin, TX. The role supports ongoing studies within the clinical research department, requiring strong interpersonal skills and collaboration in a dynamic, inclusive environment.

Responsibilities include conducting studies per FDA/GCP guidelines, accurate data recording, IP logs, and ensuring IRB approval.

Qualifications

• Bachelor's degree in a clinical or medical field.
• At least 2 years of experience as a Clinical Research Coordinator or similar.
• Solid understanding of clinical research processes, including GCP, SOPs, and safety monitoring.
• Excellent organizational skills and attention to detail.
• Strong interpersonal and communication skills; fluency in English preferred.

Responsibilities

• Conduct clinical studies in accordance with FDA/GCP and ICH regulations and guidelines.
• Accurately record patient information and test results on required forms per protocol.
• Complete IP accountability logs and related documentation when necessary.
• Report suspected non-compliance issues to relevant site staff promptly.
• Ensure IRB approval is obtained prior to study initiation and maintain compliance throughout the study duration.
• Schedule patient bookings and conduct follow‑ups.
• Record patient demographics and test/study results.

Skills

Clinical research experience

Education

Bachelor's degree in clinical/medical field

Tools

GCP knowledge

Job description

Experis Austria seeks a Clinical Research Coordinator to join a leading healthcare and clinical research organization in Lufkin, TX. The role supports ongoing studies within the clinical research department, requiring strong interpersonal skills and collaboration in a dynamic, inclusive environment.

Responsibilities include conducting studies per FDA/GCP guidelines, accurate data recording, IP logs, and ensuring IRB approval.