Clinical Research Coordinator LPN or Experienced Medical Assistant
UDEC-PIC-DPC
Chattanooga, TNFull-time
Behavioral Health Market Context
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Benefits
Health InsurancePaid Time OffDental Coverage
Job Description
Immediate hire.
General Job Duties:
Serve as a primary or backup coordinator on active studies (currently ~10 protocols)
Oversee and coordinate clinical trials and research activities
Ensure compliance with regulatory requirements, GCP, and internal SOPs
Maintain high standards of patient care and safety
Recruit study participants via Athena EMR and in-person
Assist with and perform study visits per protocol
Complete data entry and collect biological samples, vital signs, and other required assessments - phlebotomy knowledge is a must.
Administer investigational products as required by protocol
Receive, prepare, and dispense study drugs
Monitor and maintain temperature-controlled drugs and supplies
Professionally interact with investigators, team members, monitors, and vendors
Position Type: Full-time, permanent Location: On-site, Monday–Friday Location: Chattanooga, TN
General Job Duties:
Serve as a primary or backup coordinator on active studies (currently ~10 protocols)
Oversee and coordinate clinical trials and research activities
Ensure compliance with regulatory requirements, GCP, and internal SOPs
Maintain high standards of patient care and safety
Recruit study participants via Athena EMR and in-person
Assist with and perform study visits per protocol
Complete data entry and collect biological samples, vital signs, and other required assessments - phlebotomy knowledge is a must.
Administer investigational products as required by protocol
Receive, prepare, and dispense study drugs
Monitor and maintain temperature-controlled drugs and supplies
Professionally interact with investigators, team members, monitors, and vendors
Position Type: Full-time, permanent Location: On-site, Monday–Friday Location: Chattanooga, TN
Qualifications
Benefits
- •Dental insurance
- •Health insurance
- •Paid time off
- •Parental leave
- •Training & development
- •Vision insurance
Responsibilities
- •Serve as a primary or backup coordinator on active studies (currently ~10 protocols)
- •Oversee and coordinate clinical trials and research activities
- •Ensure compliance with regulatory requirements, GCP, and internal SOPs
- •Maintain high standards of patient care and safety
- •Recruit study participants via Athena EMR and in-person
- •Assist with and perform study visits per protocol
- •Complete data entry and collect biological samples, vital signs, and other required assessments - phlebotomy knowledge is a must
- •Administer investigational products as required by protocol
- •Receive, prepare, and dispense study drugs
- •Monitor and maintain temperature-controlled drugs and supplies
- •Professionally interact with investigators, team members, monitors, and vendors
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