Clinical Trials Coordinator: Drive Study Operations

Pinnacle Clinical Research; Las Vegas (NV); On-site; USD 60,000 - 85,000; Full time

Job summary

Pinnacle Clinical Research in Las Vegas, NV is seeking a Clinical Research Coordinator to manage daily trial operations, recruit and screen participants, and maintain regulatory compliance. The role requires strong communication, organization, and multitasking abilities in a fast-paced environment.

The ideal candidate has 1–2 years of clinical research experience, proficiency in Microsoft Office and CTMS, and knowledge of ICH/GCP.

Qualifications

• High school diploma or GED required.
• Bachelor’s Degree in a scientific area preferred or equivalent combination of education, training, and experience.
• 1 year of experience as a Clinical Research Assistant or Coordinator.
• 1-2 years of experience in Clinical Research.
• Proficient in all Microsoft Office applications and CRIO or equivalent CTMS.
• Must have strong knowledge of ICH/GCP guidelines.
• Must complete GCP training before interacting with participants and recertify every 2 years or as applicable.
• Trained and certified in Fibroscan and memory screens as required by the study portfolio and individual experience. Training to be provided.
• Must have basic life support (BLS) training, provided during onboarding.
• Demonstrated organizational skills and outstanding time management, including keen attention to detail, with the ability to track multiple projects at one time.
• Strong written and oral communication skills.
• Knowledge of basic medical terminology.
• Possess impeccable integrity and personal and professional values that are consistent with PCR's high standards and mission.
• Comply with the company policies, code of ethics, and guiding values always.
• Proficient in Spanish and English preferred.

Responsibilities

• Manage day-to-day operations of assigned clinical trials and ensure protocol and regulatory requirements are followed.
• Recruit and screen study participants, document and report daily operations, and report participant status.
• Develop workflows to complete activities promptly and maintain data confidentiality per FDA/ICH GCP/HIPAA guidelines.
• Collaborate with sponsors, vendors, and team members; participate in monitoring visits and audits.
• Track enrollment and study status reports to meet recruitment goals and site milestones.

Skills

Strong communication

Time management

Detail oriented

Organizational skills

Bilingual Spanish/English

Microsoft Office

CRIO/CTMS experience

Education

Bachelor’s degree in science

High school diploma or GED

Tools

CRIO/CTMS

Job description

Pinnacle Clinical Research in Las Vegas, NV is seeking a Clinical Research Coordinator to manage daily trial operations, recruit and screen participants, and maintain regulatory compliance. The role requires strong communication, organization, and multitasking abilities in a fast-paced environment.

The ideal candidate has 1–2 years of clinical research experience, proficiency in Microsoft Office and CTMS, and knowledge of ICH/GCP.