Clinical Research Coordinator
eTeam Inc
Job Title: Clinical Research Coordinator
Location: Loma Linda, CA
Duration: 9 Months
Pay Rate: $36-$38/hr on W2
Timing: Mon-Fri 8am-5pm Summary
Location: Loma Linda, CA
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.
- 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.
- 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.
- 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.
Vacancy posted 5 days ago
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