Clinical Research Coordinator

Numinus

Draper, UTFull-time

Behavioral Health Market Context

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Benefits

Paid Time OffDental CoverageHealth Insurance

Job Description

our team!

Numinus values diversity and strives to create an inclusive work environment. We respect and celebrate individuals for their differences and encourage applicants from all backgrounds to apply.

We are looking for someone who is highly motivated, organized, and able to work independently to join our team. This Clinical Research Coordinator position will be in our Draper Clinic. (in-person not remote)

Responsibilities:
• Coordinating and performing responsibilities related to research participants including pre-screening, scheduling, overseeing patient visits, and obtaining informed consent
• Preparing, submitting, and maintaining IRB regulatory documents
• Ensuring quality data and compliance to the protocol
• Entering data into EDC systems
• Conducting ECG’s
• Performing blood draws
• Packaging and shipping labs
• Obtaining medical history
• Documenting, reporting, and tracking AE’s and SAE’s
• Preparing for site visits or audits from sponsors and/or other agencies
• Ordering supplies

Qualifications:
• 3 years experience as a Clinical Research Coordinator
• Must have High School Diploma or GED, Bachelor’s Degree preferred
• Phlebotomist Experience

Benefits:
• 401(k) matching
• Medical, Dental, Vision, & Life insurance
• Flexible spending account
• Paid time off

Schedule:
• Day shift
• Monday to Friday

Requirements

Education:
• High school or equivalent (Required)

Experience:
• Clinical Research Coordinator: 3 years (Required)

License/Certification:
• Phlebotomy Certification (Preferred)

Qualifications

  • 3 years experience as a Clinical Research Coordinator
  • Phlebotomist Experience
  • High school or equivalent (Required)
  • Clinical Research Coordinator: 3 years (Required)

Benefits

  • 401(k) matching
  • Medical, Dental, Vision, & Life insurance
  • Flexible spending account
  • Paid time off

Responsibilities

  • Coordinating and performing responsibilities related to research participants including pre-screening, scheduling, overseeing patient visits, and obtaining informed consent
  • Preparing, submitting, and maintaining IRB regulatory documents
  • Ensuring quality data and compliance to the protocol
  • Entering data into EDC systems
  • Conducting ECG’s
  • Performing blood draws
  • Packaging and shipping labs
  • Obtaining medical history
  • Documenting, reporting, and tracking AE’s and SAE’s
  • Preparing for site visits or audits from sponsors and/or other agencies
  • Ordering supplies


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