Clinical Research Coordinator II - Patient-Focused Trials

Care Access

St. Louis (MO)

On-site

USD 60,000 - 90,000

Full time

3 days ago
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Benefits offered by this job

Paid Time Off and Holidays
100% Employer-paid medical, dental, &
Health Savings Account and Flexible SP
Bi-weekly HSA employer contribution
Disability insurance (short & long)
401(k) with company match
Relocation support

Job summary

Care Access is hiring a Clinical Research Coordinator to ensure GCP-compliant screening, enrollment and monitoring of study subjects across clinical trials. The role emphasizes regulatory adherence and strong patient relations, working with diverse teams.

You'll coordinate site visits, manage data entry, and support recruitment efforts, with opportunities to mentor junior CRC staff and contribute to study success.

Qualifications

  • Bachelor’s degree preferred or equivalent experience.
  • 3 years prior Clinical Research Coordinator experience required.
  • Recent phlebotomy experience required.

Responsibilities

  • Screen, enroll, and monitor study subjects per protocol and GCP.
  • Maintain FDA regulations and ICH guidelines across trials.
  • Foster effective relationships with participants and study staff.
  • Coordinate site visits and manage regulatory documents.
  • Mentor CRC I peers and support onboarding.
  • Identify AEs/SAEs and report to PI and Sponsor as needed.
  • Assist in recruitment planning and materials development.
  • Ensure training is completed prior to trial conduct.

Skills

GCP knowledge
Regulatory compliance
Communication skills
Attention to detail
Leadership

Education

Bachelor’s Degree preferred

Tools

Clinical trials database
IVR systems
Electronic data capture
MS Word
MS Excel

Job description

Care Access is hiring a Clinical Research Coordinator to ensure GCP-compliant screening, enrollment and monitoring of study subjects across clinical trials. The role emphasizes regulatory adherence and strong patient relations, working with diverse teams.

You'll coordinate site visits, manage data entry, and support recruitment efforts, with opportunities to mentor junior CRC staff and contribute to study success.

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