Clinical Research Coordinator
25–35 an hour
Behavioral Health Market Context
Apply Nowvia Indeed
Benefits
Paid Time OffHealth Insurance
Job Description
ndent study coordination.
Key Responsibilities:
Coordinate clinical trials in compliance with protocol, GCP, and site SOPs
Conduct patient visits including informed consent, vitals, ECGs, and sample collection
Manage patient recruitment, screening, and retention
Perform accurate and timely data entry (EDC) and resolve queries
Maintain source documentation and regulatory binders
Track and report adverse events (AEs/SAEs)
Communicate with PIs, sponsors, and CROs
Support monitoring visits, audits, and study close-out
Qualifications
Required:
• 1–3 years of clinical research experience (CRC or Research Assistant)
• Understanding of GCP and clinical trial processes
• Strong organizational and time management skills
• Ability to manage multiple studies and priorities
• Professional communication skills
• Reliable and punctual
Preferred:
• Cardiology research experience
• Phlebotomy skills
• Experience independently managing study visits
• Familiarity with EDC systems and query resolution
• ACRP or SOCRA certification (or working toward certification)
Compensation & Growth
• $25–$35/hour (based on experience)
• Growth into independent CRC role
• Certification support after tenure milestones
Pay: $25.00 - $35.00 per hour
Benefits:
• Health insurance
• Paid time off
Application Question(s):
• Describe a time you made a mistake in a clinical or work setting. What happened and how did you handle it?
• How do you prioritize when managing multiple patients or study tasks at the same time?
• Do you have experience conducting patient visits (e.g., consent, vitals, ECGs)? Please describe.
Work Location: In person
Key Responsibilities:
Coordinate clinical trials in compliance with protocol, GCP, and site SOPs
Conduct patient visits including informed consent, vitals, ECGs, and sample collection
Manage patient recruitment, screening, and retention
Perform accurate and timely data entry (EDC) and resolve queries
Maintain source documentation and regulatory binders
Track and report adverse events (AEs/SAEs)
Communicate with PIs, sponsors, and CROs
Support monitoring visits, audits, and study close-out
Qualifications
Required:
• 1–3 years of clinical research experience (CRC or Research Assistant)
• Understanding of GCP and clinical trial processes
• Strong organizational and time management skills
• Ability to manage multiple studies and priorities
• Professional communication skills
• Reliable and punctual
Preferred:
• Cardiology research experience
• Phlebotomy skills
• Experience independently managing study visits
• Familiarity with EDC systems and query resolution
• ACRP or SOCRA certification (or working toward certification)
Compensation & Growth
• $25–$35/hour (based on experience)
• Growth into independent CRC role
• Certification support after tenure milestones
Pay: $25.00 - $35.00 per hour
Benefits:
• Health insurance
• Paid time off
Application Question(s):
• Describe a time you made a mistake in a clinical or work setting. What happened and how did you handle it?
• How do you prioritize when managing multiple patients or study tasks at the same time?
• Do you have experience conducting patient visits (e.g., consent, vitals, ECGs)? Please describe.
Work Location: In person
Qualifications
- •The ideal candidate is reliable, detail-oriented, and capable of managing multiple responsibilities while working toward independent study coordination
- •1–3 years of clinical research experience (CRC or Research Assistant)
- •Understanding of GCP and clinical trial processes
- •Strong organizational and time management skills
- •Ability to manage multiple studies and priorities
- •Professional communication skills
- •Reliable and punctual
- •Do you have experience conducting patient visits (e.g., consent, vitals, ECGs)?
Benefits
- •Compensation & Growth
- •$25–$35/hour (based on experience)
- •Growth into independent CRC role
- •Certification support after tenure milestones
- •Pay: $25.00 - $35.00 per hour
- •Health insurance
- •Paid time off
Responsibilities
- •This is a hands-on, patient-facing role in a fast-paced clinical environment
- •Coordinate clinical trials in compliance with protocol, GCP, and site SOPs
- •Conduct patient visits including informed consent, vitals, ECGs, and sample collection
- •Manage patient recruitment, screening, and retention
- •Perform accurate and timely data entry (EDC) and resolve queries
- •Maintain source documentation and regulatory binders
- •Track and report adverse events (AEs/SAEs)
- •Communicate with PIs, sponsors, and CROs
- •Support monitoring visits, audits, and study close-out
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