Job Title:
Clinical Research Coordinator
Location:
Fountain Valley, California
Office-based / On-site
Work Schedule:
Part-time
24 hours per week
Job ID:
R1503633
Compensation:
Base pay range: $35.00 – $42.00 per hour
Actual pay varies based on:
Qualifications (knowledge, skills, education, experience)
Location
Schedule (full-time/part-time)
May include incentive plans, bonuses, and benefits
Key Responsibilities:
Clinical Procedures & Patient Care
Perform phlebotomy, including pediatric patients
Conduct complex clinical procedures: ECG, spirometry, vital signs, sample collection
Maintain a safe environment adhering to Health and Safety policies
Advocate for volunteers and address their concerns proactively
Assist registered and unregistered staff in clinical coordination and patient care
Report deviations from normal practice to senior staff
Study Support & Coordination
Coordinate clinical research studies under the principal investigator’s supervision
Review study protocols, case report forms (CRFs), and electronic data capture systems
Participate in project team meetings and daily huddles
Prepare clinical setups: label specimen tubes, set up equipment and documents
Plan logistical activities and procedures as per protocol
Generate volunteer instructions and secure necessary supplies and equipment
Prepare and deliver study-specific training materials
Troubleshoot study-related issues
Data Management & Compliance
Assist with data quality checks and query resolution to ensure protocol adherence
Recruit, screen, and orient volunteers to study procedures and timelines
Manage proper administration and custody of study drugs per SOPs
Collect, record, and report clinical data accurately in CRFs
Collaborate with investigators to report adverse and serious adverse events
Cooperate with study monitors and facilitate monitoring visits
Follow ICH GCP guidelines and site standard operating procedures
Qualifications:
Education & Experience
High School Diploma (or equivalent)
Minimum 1 year relevant clinical research experience
Preferred
At least 1 year clinical research setting experience
Pediatric experience and community outreach involvement preferred
Skills & Knowledge
Knowledge of clinical trials and Good Clinical Practices (GCP)
Familiarity with study protocols, consent forms, and schedules
Skilled in clinical procedures and medical terminology
Strong attention to detail
Ability to maintain effective working relationships with coworkers, patients, and clients
Certifications & Licenses
Applicable certifications/licenses required by regulatory bodies, company, state, or country
Additional Information:
This position is not eligible for sponsorship
Tags: #LI-CES, #LI-DNP, #LI-HCP, #ONSITE
About IQVIA:
IQVIA is a global leader in clinical research, healthcare intelligence, and life sciences consulting, working to accelerate medical innovation and improve patient outcomes.
Learn more: https://jobs.iqvia.com
Equal Opportunity Employer: https://jobs.iqvia.com/eoe
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