Clinical Research Coordinator II - On-Site Trials

Care Access

Houston (TX)

On-site

USD 60,000 - 90,000

Full time

3 days ago
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Benefits offered by this job

PTO
Employer-paid medical
Health Savings Account
Disability insurance
401(k) with company match
Relocation assistance

Job summary

Care Access is seeking aClinical Research Coordinator to support screening, enrollment, and monitoring of study subjects in Houston, TX. The role emphasizes GCP compliance, FDA regulations, and strong patient coordination to ensure protocol adherence and high-quality data.

You will collaborate with investigators and site staff, manage regulatory documents, and mentor CRC I peers while maintaining timely visits and accurate data capture.

Qualifications

  • Bachelor’s degree preferred, or equivalent combination of education, training and experience.
  • 3 years prior Clinical Research Coordinator experience required
  • Recent phlebotomy experience required

Responsibilities

  • Screen, enroll and monitor clinical trial subjects per protocol.
  • Maintain regulatory compliance and GCP adherence.
  • Prescreen candidates and obtain informed consent.
  • Collect and review data, blood draws, vital signs, ECGs; alert investigators as needed.
  • Coordinate visits and site communications with investigators and staff.
  • Mentor CRC I peers and assist with onboarding.

Skills

SOP compliance
GCP knowledge
FDA regulations
Independent worker
Communication skills
Team collaboration
Attention to detail
Clinical trials software
Data capture
Problem solving

Education

Bachelor’s degree or equivalent

Tools

MS Word
Excel
IVR systems
EDC systems
Clinical trials database

Job description

Care Access is seeking aClinical Research Coordinator to support screening, enrollment, and monitoring of study subjects in Houston, TX. The role emphasizes GCP compliance, FDA regulations, and strong patient coordination to ensure protocol adherence and high-quality data.

You will collaborate with investigators and site staff, manage regulatory documents, and mentor CRC I peers while maintaining timely visits and accurate data capture.

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