Clinical Research Coordinator: Manage Trials & Care

Pinnacle Clinical Research

Austin (TX)

On-site

USD 52,000 - 76,000

Full time

14 days+

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Benefits offered by this job

401k
Medical insurance
Paid time off
Holidays 14
Scrub vouchers

Job summary

Summit Clinical Research Solutions in Austin, TX is seeking a Clinical Research Coordinator to manage day-to-day trial operations, recruit and screen participants, and ensure protocol and regulatory compliance. This role emphasizes communication, organization, and collaborative problem-solving to support quality participant care and study success.

The coordinator will work closely with sponsors, sites, and vendors, maintain study documentation in CRIO/CTMS, and help drive enrollment and data

Qualifications

  • Requires high school diploma or GED; Bachelor’s degree preferred.
  • 1 year of experience as Clinical Research Assistant/Coordinator.
  • Strong knowledge of ICH/GCP guidelines and GCP training; recertification every 2 years.

Responsibilities

  • Manage day-to-day operations of assigned clinical trials and ensure protocol/regulatory adherence.
  • Recruit and screen study participants; obtain informed consent and coordinate visits.
  • Maintain participant privacy and data integrity per FDA, ICH GCP, HIPAA requirements.

Skills

Strong ICH/GCP knowledge
Excellent communication
Organizational skills
Attention to detail
Team collaboration
Problem-solving
Multi-tasking
Bilingual Spanish & English (preferred

Education

Bachelor’s Degree in science or related field
GED acceptable with experience

Tools

CRIO/CTMS
Microsoft Office

Job description

Summit Clinical Research Solutions in Austin, TX is seeking a Clinical Research Coordinator to manage day-to-day trial operations, recruit and screen participants, and ensure protocol and regulatory compliance. This role emphasizes communication, organization, and collaborative problem-solving to support quality participant care and study success.

The coordinator will work closely with sponsors, sites, and vendors, maintain study documentation in CRIO/CTMS, and help drive enrollment and data

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