Responsibilities
- Collect blood and urine samples and process specimens through centrifugation, aliquoting, and labeling
- Assemble subject-specific lab kits according to study protocols
- Ship biological samples in compliance with IATA regulations and study requirements
- Maintain accurate records including specimen logs, shipping documentation, and temperature monitoring
- Perform point-of-care testing such as urine drug screens and pregnancy tests
- Support patient procedures including vital sign measurement, ECGs, and exam preparation
- Sanitize laboratory equipment and workspaces daily
- Calibrate equipment and document compliance with safety standards including OSHA and HIPAA
- Record lab data accurately in electronic and paper formats using systems like CRIO or eCRFs
- Address and resolve data queries in electronic databases
- Ensure data entries and study documents are complete and correct
- Participate in quality assurance activities to maintain regulatory standards
- Track and manage inventory of lab kits and supplies
- Order dry ice and essential laboratory materials
- Dispose of expired kits following protocol and maintain disposal logs
- Help develop training resources and lab manuals tailored to specific studies
- Coordinate with study staff and medical personnel to fulfill visit requirements
- Provide assistance during infusion monitoring under the supervision of a clinician
Requirements
- High School Diploma or GED required
- Certification in phlebotomy or equivalent training required
- Minimum of one year of experience in a clinical laboratory environment
- Ability to safely manage infectious and hazardous materials
- Physically capable of lifting up to 50 pounds and standing or moving for extended periods
- Strong organizational, time management, and multitasking abilities
- Excellent verbal and written communication skills with strong interpersonal competence
- Capable of working both independently and collaboratively within a multidisciplinary team
- Demonstrates professionalism and a customer-focused approach
Nice to Have
- Bachelor's degree preferred
- Experience with Phase I-IV clinical trials and knowledge of GCP, GLP, and ICH guidelines preferred
- Proficiency in Microsoft Office applications and database systems
Benefits
- Medical, dental, and vision insurance coverage
- Health Savings Account (HSA) and Flexible Spending Account (FSA) options
- Paid Time Off (PTO)
- Disability, accident, and life insurance benefits
Compensation
$22 - $26/hr
Work Arrangement
On-site
Team
Member of the clinical research and laboratory operations team, reporting to the Site Director
Schedule
Mondays through Fridays, 8:00am - 5:00pm
Location
Onsite in Riverside, CA
Type
Regular Full-time Employee
Pay Range
$22 - $26/hr
Not specified
