Clinical Research Coordinator

eTeam Inc.

Linda, CA

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JOB DETAILS

SALARY

$36–$38 Per Hour

SKILLS

Adverse Events, Budget Management, Cardiac Monitoring, Case Report Form (CRF), Clinical Assessment, Clinical Research, Clinical Trial, Conduct Studies, Data Management, Data Quality, Database Programming, Detail Oriented, Documentation, Electrocardiogram, Electronic Data Capture (EDC), GCP (Good Clinical Practices), High School Diploma, Informed Consent, Interpersonal Skills, Laboratory Management, Logistics Management, Medical Records, Medical Terminology, Medical Treatment, Microsoft Access Database, Microsoft Excel, Microsoft Office, Microsoft Outlook, Microsoft Word, Organizational Skills, Paint Shop Pro Tubes, Record Keeping, Regulations, Research Protocols, Sample/Specimen Processing, Specimen Collection, Staff Training, Standard Operating Procedures (SOP), Telemetry, Time Management

LOCATION

Linda, CA

POSTED

21 days ago

Job Title: 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

About the Company

eTeam Inc.

Looking for a great job? Join eTeam. We’re looking for talented staffing professionals to join our staff. We also provide contract assignments and full-time jobs at Fortune 2000 Companies. We’ve been named one of the best companies to work for by Staffing Industry Analysts and New Jersey Business.

COMPANY SIZE

100 to 499 employees

INDUSTRY

Other/Not Classified

FOUNDED

1998

WEBSITE