Clinical Trials Coordinator: Drive Study Ops & Patient Care

Pinnacle Clinical Research

Brownsville (TX)

On-site

USD 52,000 - 68,000

Full time

14 days+

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Job summary

Summit Clinical Research Solutions in Brownsville, TX is seeking a dedicated Clinical Research Coordinator to manage day-to-day trial operations, recruit and screen participants, and ensure study protocols and regulatory requirements are followed.

You will collaborate with sponsors, vendors, and team members, maintain accurate documentation, and support safety reporting, CAPA processes, and study milestones while delivering high-quality participant care.

Qualifications

  • ,

Responsibilities

  • Exercise judgement within protocol and SOPs.
  • Maintain participant privacy and data confidentiality per FDA, ICH GCP, HIPAA.
  • Complete study-directed assessments and scheduling.
  • Document and manage data per regulatory guidelines.
  • Liaise with sponsors and external vendors.
  • Manage participant enrollment and engagement from recruitment to study completion.
  • Respond to information requests promptly.
  • Identify opportunities to improve participant care.
  • Resolve study-related issues with a solutions-oriented mindset.
  • Build productive relationships to achieve research outcomes.
  • Coordinate multiple projects with competing deadlines.
  • Attend study-related visits and monitoring sessions.
  • Track enrollment and site status reports.

Skills

Proficient in Microsoft Office
Strong communication
Organizational skills
Problem-solving
Team collaboration
Bilingual Spanish/English

Education

Bachelor's Degree in a scientific field
High school diploma or GED

Tools

CRIO/CTMS
Microsoft Office

Job description

Summit Clinical Research Solutions in Brownsville, TX is seeking a dedicated Clinical Research Coordinator to manage day-to-day trial operations, recruit and screen participants, and ensure study protocols and regulatory requirements are followed.

You will collaborate with sponsors, vendors, and team members, maintain accurate documentation, and support safety reporting, CAPA processes, and study milestones while delivering high-quality participant care.

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