Clinical Research Coordinator II: Trials & Compliance

Pinnacle Clinical Research; Farmers Branch (TX); On-site; USD 55,000 - 75,000; Full time

Benefits offered by this job

401k

Medical, dental, vision insurance

Paid time off

Job summary

Summit Clinical Research Solutions is seeking a Clinical Research Coordinator II to oversee daily trial activities in a fast-paced environment. You will coordinate participant recruitment, screenings, and study documentation while ensuring strict regulatory compliance and data integrity.

The role requires strong communication, organization, and collaboration with sponsors, vendors, and team members to deliver high-quality participant care and study outcomes.

Qualifications

• High school diploma or GED required; a scientific bachelor’s preferred.
• 2–3 years of experience as a Clinical Research Coordinator.
• 3–4 years of experience in clinical research.
• Strong knowledge of ICH/GCP guidelines; GCP training required and recertification every 2 years.

Responsibilities

• Manage day-to-day operations of assigned clinical trials.
• Recruit and screen study participants and document activities.
• Ensure compliance with protocol, regulatory requirements, and study milestones.
• Maintain participant privacy and data confidentiality per FDA, ICH GCP, HIPAA, and IRB policies.
• Mentor less experienced staff and coordinate with sponsors and vendors.

Skills

Multitasking

Communication skills

Documentation & data management

Bilingual English/Spanish

Team collaboration

Regulatory knowledge

Education

GED

Bachelor’s degree in a scientific field

Promotion from Clinical Research Coordinator I

Tools

Microsoft Office

CRIO/CTMS

Data management systems

Job description

Summit Clinical Research Solutions is seeking a Clinical Research Coordinator II to oversee daily trial activities in a fast-paced environment. You will coordinate participant recruitment, screenings, and study documentation while ensuring strict regulatory compliance and data integrity.

The role requires strong communication, organization, and collaboration with sponsors, vendors, and team members to deliver high-quality participant care and study outcomes.