Clinical Research Coordinator

Clinical Research Coordinator

Location: Loma Linda, CA 92354

Duration: 9 Months

Pay Rate: $36$38/hr on W2

Timing: Mon-Fri 8am-5pm

Summary

• Perform clinical procedures to collect, record, and interpret patient data per study protocols, SOPs, and GCP guidelines.
• Support investigators with study execution and assist with daily workload planning.

Responsibilities

• Review study protocols, CRFs, study-specific documents, and electronic data capture systems.
• Attend all required study meetings.
• Prepare and submit regulatory/ethics documentation per FDA and other regulating bodies.
• Recruit and screen potential study participants and maintain screening logs.
• Orient subjects to study procedures, timelines, and expectations.
• Create and maintain source documentation based on protocol requirements.
• Schedule and conduct study visits and perform assigned study procedures.
• Collect, record, and manage research data, ensuring accuracy and completeness.
• Prepare specimen collection tubes and manage lab logistics.
• Perform clinical procedures such as ECGs, vital signs, spirometry, cannulation, dose verification, sample collection, and cardiac telemetry monitoring.
• Monitor subject safety and report adverse events to the appropriate medical personnel.
• Communicate with research subjects and address study-related inquiries or issues.
• Participate in daily huddles to confirm study tasks and ensure standards are met.
• Assist with data quality checks and query resolution.
• Record, interpret, and report study findings to support database development.
• Support investigators in meeting study objectives on time and within budget.
• Train new site staff on study-specific procedures and maintain training records.
• Prepare for and participate in monitoring visits, audits, and regulatory inspections.
• Support staffing and scheduling efforts for research studies.

Required Knowledge, Skills & Abilities

• Solid knowledge of clinical trials and study operations.
• Strong understanding of departmental SOPs, protocols, consent forms, and study schedules.
• Knowledge of medical terminology.
• Proficiency in MS Office applications (Excel, Word, Outlook, Access).
• Excellent interpersonal skills.
• Strong attention to detail.
• Ability to build and maintain effective working relationships with team members, managers, and clients.

Minimum Education & Experience

• High school diploma required; BS degree preferred.
• Relevant experience in a clinical or medical setting, or an equivalent combination of education and training.
• Certifications and licenses as required by applicable regulations.

Additional Skills/Qualifications: Prior oncology clinical trial experience, EDC experience, biospecimen handling and shipping experience