Clinical Research Coordinator — Collaborative Trials & Impact

Socket.dev; Brownsville (TX); On-site; USD 42,000 - 64,000; Full time

Benefits offered by this job

401k

Medical, dental, vision, disability & 

PTO 3 weeks

14 paid holidays

Scrub uniform voucher

Job summary

Summit Clinical Research Solutions is seeking a detail-oriented Clinical Research Coordinator to oversee daily trial operations, ensure compliance with study protocols and regulatory requirements, and recruit participants. You will collaborate closely with sponsors, vendors, and internal teams to maintain participant care and data integrity.

The ideal candidate has strong organizational and communication skills, experience in clinical research, and familiarity with ICH/GCP guidelines.

Qualifications

• High School Diploma or GED required.
• Bachelor’s Degree in a scientific area preferred or equivalent.
• 1 year of experience as a Clinical Research Assistant or Coordinator.
• 1-2 years of experience in Clinical Research.
• Strong knowledge of ICH/GCP guidelines.
• GCP training required and recertification every 2 years.
• Training in Fibroscan and memory screens as required; training provided.
• BLS training provided on onboarding.
• Proficient in English and Spanish preferred.

Responsibilities

• Manage day-to-day clinical trial operations and ensure protocol/regulatory compliance.
• Recruit and screen participants and document study activities.
• Maintain confidentiality and data integrity per FDA/ICH/GCP/HIPAA.
• Coordinate with sponsors and vendors; support monitoring visits and audits.
• Track enrollment and study status; communicate findings to team.
• Prepare memos, emails, and reports and assist with CAPA processes.

Skills

Communication skills

Multitasking

Organizational skills

Time management

Attention to detail

Bilingual Spanish/English

Education

High School Diploma/GED

Bachelor’s degree preferred (scientific area)

Tools

CRIO/CTMS

Microsoft Office

Job description

Summit Clinical Research Solutions is seeking a detail-oriented Clinical Research Coordinator to oversee daily trial operations, ensure compliance with study protocols and regulatory requirements, and recruit participants. You will collaborate closely with sponsors, vendors, and internal teams to maintain participant care and data integrity.

The ideal candidate has strong organizational and communication skills, experience in clinical research, and familiarity with ICH/GCP guidelines.