Clinical Research Coordinator I
The Clinical Research Coordinator I (CRC I) supports the daily operations of assigned clinical trials.  This role is based in San Antonio, TX. 

Job Responsibilities:

• Patient Interaction & Education:
  

  • Inform patients and caregivers about study procedures and expected outcomes.
    

  
  

• Study Compliance:
  

  • Monitor study activities to ensure adherence to protocols and regulatory guidelines.
    

  
  

• Data Management:
  

  • Accurately complete and enter source documentation and case report forms.
    

  • Resolve data queries promptly.
    

  
  

• Inventory & Logistics:
  

  • Manage and dispense study supplies and medications.
    

  • Maintain accurate records of study activity.
    

  
  

• Clinical Procedures:
  

  • Perform specific protocol procedures like taking vital signs, collecting specimens, and administering medications.
    

  
  

• Adverse Event Monitoring:
  

  • Record and report adverse events and side effects.
    

  
  

• Quality Assurance:
  

  • Participate in quality assurance audits.
    

  
  

• Administrative Tasks:
  

  • Maintain accurate records and logs.
    

  • Label and organize study materials.
    

Required Skills:

• Clinical Research Experience: 6 months – 2 years preferred.
  

• Teamwork & Independence: Ability to work both independently and collaboratively.
  

• Attention to Detail: Meticulous data entry and record-keeping skills.
  

• Communication: Effective communication with patients, investigators, and other team members.
  

• Organization: Ability to manage multiple tasks and prioritize effectively.

Education & Experience:

• High School Diploma or GED required.
  

• Some college or relevant medical certification is preferred.

Job Details:

• Contract
  

• M-F; 8am-5pm or 7am-4pm
  

• Possible overtime
  

• $22-24 pay rate

9689536