Clinical Research Coordinator

at  Numinus

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.

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
• Maintaining various logs including temperature, screening and enrollment, etc.

REQUIREMENTS

Qualifications:

• 3 years experience as a Clinical Research Coordinator required
• Must have High School Diploma or GED, Bachelor’s Degree preferred
• Nursing degree preferred (RN/BSN)
• NCMSHT (Nationally Certified Multi-Skilled Healthcare Technician) ideal
• CCRC credential preferred
• Phlebotomist Certification ideal

Job Type: Full-time

Benefits:

• 401(k)
• 401(k) matching
• Dental insurance
• Flexible spending account
• Health insurance
• Paid time off
• Vision insurance

Schedule:

• 8 hour shift
• Day shift
• Monday to Friday

Requirements

REQUIREMENTS

Education:

• High school or equivalent (Required)

Experience:

• Clinical Research Coordinator: 3 years (Required)

License/Certification:

• CCRC Credential (Certified Clinical Research Coordinator) (Preferred)
• Phlebotomy Certification (Preferred)

• 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
• Maintaining various logs including temperature, screening and enrollment, etc