Clinical Research Coordinator: Drive Trials & Care

Pinnacle Clinical Research- A Summit Solution; Ridgewood (NJ); On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

401k

Full benefits package

Paid time off

Company holidays

Scrub uniform voucher

Job summary

Summit Clinical Research Solutions is seeking a Clinical Research Coordinator to manage day‑to‑day trial operations, recruit and screen participants, and ensure protocol and regulatory compliance.

The role requires strong communication, multi‑tasking, and collaboration with sponsors and vendors. GCP/ICH knowledge and BLS may be required; Spanish/English skills are a plus. Reporting to the Clinical Operations Manager and supporting multiple studies.

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.
• Proficient in MS Office and CRIO/CTMS.
• Strong knowledge of ICH/GCP guidelines; GCP training required.
• BLS training; training on Fibroscan/memory screens as needed.
• Spanish and English language abilities preferred.

Responsibilities

• Execute clinical trial activities within protocol SOPs and regulatory guidelines.
• Maintain participant privacy and data confidentiality (FDA, ICH GCP, HIPAA).
• Complete study assessments and coordination activities (consent, histories, vitals).
• Manage data entry and documentation per GCP.
• Liaise with sponsors and vendors; participate in monitoring visits.
• Oversee participant management from recruitment to completion.
• Respond to information requests promptly; identify ways to improve participant care.
• Develop relationships to achieve high research outcomes.
• Coordinate multiple projects with competing priorities and deadlines.
• Attend investigator meetings and study visits as required.
• Track enrollment and study status reports to meet goals.

Skills

Communication skills

Organization & time management

Multitasking

Attention to detail

Bilingual (Spanish & English)

Education

High school diploma or GED

Bachelor’s Degree preferred

Tools

Microsoft Office

CRIO/CTMS

Job description

Summit Clinical Research Solutions is seeking a Clinical Research Coordinator to manage day‑to‑day trial operations, recruit and screen participants, and ensure protocol and regulatory compliance.

The role requires strong communication, multi‑tasking, and collaboration with sponsors and vendors. GCP/ICH knowledge and BLS may be required; Spanish/English skills are a plus. Reporting to the Clinical Operations Manager and supporting multiple studies.