Clinical Trials Specialist

5 days ago


Lufkin, Texas, United States SiteBridge Research, Inc. Full time
About Our Team

We are a community-focused integrated research organization, building a national network of community practices to deliver world-class industry-sponsored clinical research. At SiteBridge Research, Inc., we value diversity and do not discriminate based on race, religion, color, national origin, sex, sexual orientation, age, veteran status, disability status, or any other applicable characteristics protected by law.

We are seeking an experienced Clinical Research Coordinator to join our team in Lufkin, TX. This is a unique opportunity to work in a collaborative environment, ensuring the successful conduct of clinical trials and maintaining the operational excellence of our site. The combined pay range for this role is $26 - $36/hour, based on skills and experience relevant to our needs for the role.

Key Responsibilities:

  • Direct the request, collection, labeling, storage, or shipment of interventional products
  • Ensure collection of specimens, questionnaire information, and input of data and patient information into electronic clinical systems
  • Monitor the enrollment status of participants at the site for each specific clinical study

Requirements:

  • Bachelor's degree in a relevant life science discipline; LVN or RN preferred; certification as CCRC/CCRP a plus
  • 2+ years of previous experience working in a clinical setting; number of years of clinical site/trials experience will determine position level
  • Working knowledge of FDA & ICH GCP regulations and guidelines
  • Strong preference for experience with late phase and observational clinical research


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