Clinical Research Coordinator - 247849 at Medix™ Toledo, OH
Medix™
Behavioral Health Market Context
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Job Description
ng protocol compliance, regulatory accuracy, and exceptional patient care.
Key Responsibilities
• Coordinate participant care and study activities in accordance with protocol and GCP guidelines.
• Obtain informed consent and maintain accurate source documentation.
• Report adverse events and deviations per regulatory requirements.
• Dispense and instruct participants on investigational products.
• Manage data entry, resolve queries, and maintain essential study documents.
• Support site visits, audits, and inspections.
• Collaborate with investigators and study teams to ensure quality and compliance.
Qualifications
• Minimum 3 years of clinical research experience
• Experience in a patient-facing research role (CRC, MA, EMT, or Phlebotomist)
• Proven ability to manage multiple industry-sponsored studies
• Working knowledge of GCP, FDA, and HIPAA regulations
• Bachelor’s degree and/or nephrology experience preferred
Key Responsibilities
• Coordinate participant care and study activities in accordance with protocol and GCP guidelines.
• Obtain informed consent and maintain accurate source documentation.
• Report adverse events and deviations per regulatory requirements.
• Dispense and instruct participants on investigational products.
• Manage data entry, resolve queries, and maintain essential study documents.
• Support site visits, audits, and inspections.
• Collaborate with investigators and study teams to ensure quality and compliance.
Qualifications
• Minimum 3 years of clinical research experience
• Experience in a patient-facing research role (CRC, MA, EMT, or Phlebotomist)
• Proven ability to manage multiple industry-sponsored studies
• Working knowledge of GCP, FDA, and HIPAA regulations
• Bachelor’s degree and/or nephrology experience preferred
Qualifications
- •Minimum 3 years of clinical research experience
- •Experience in a patient-facing research role (CRC, MA, EMT, or Phlebotomist)
- •Proven ability to manage multiple industry-sponsored studies
- •Working knowledge of GCP, FDA, and HIPAA regulations
Benefits
- •Full-Time | Monday–Friday, 9AM–5PM | $65,000–$80,000/year
Responsibilities
- •This role coordinates all aspects of clinical trial conduct—from participant screening through study completion—ensuring protocol compliance, regulatory accuracy, and exceptional patient care
- •Coordinate participant care and study activities in accordance with protocol and GCP guidelines
- •Obtain informed consent and maintain accurate source documentation
- •Report adverse events and deviations per regulatory requirements
- •Dispense and instruct participants on investigational products
- •Manage data entry, resolve queries, and maintain essential study documents
- •Support site visits, audits, and inspections
- •Collaborate with investigators and study teams to ensure quality and compliance
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