HIGHLIGHTS

Full-time, Monday-Friday schedule: 8:00 AM-5:00 PM, with occasional weekend availability needed Located onsite in West Covina, California Hourly compensation of $23-$33, based on relevant experience Comprehensive benefits including medical, dental, vision, 401(k) with employer match, tuition reimbursement, PTO, holidays, parental leave, and more Opportunity to build hands-on clinical research experience in cardiovascular and metabolic studies Join a fast-growing clinical research network with 30+ sites across 10+ states and meaningful long-term career development potential COMPANY Our client is a leading and rapidly expanding clinical research site network focused on helping bring new treatments and medical advances to patients. Their W. Covina location has served the Greater Los Angeles community for many years and conducts cardiovascular and metabolic clinical trials. This is an entrepreneurial, collaborative environment where motivated team members can grow alongside the organization as it continues to expand in 2025 and beyond.

POSITION

The Clinical Research Assistant will support clinical trial activities under the direction of site leadership and Clinical Research Coordinators. This person will help keep study visits organized, support patients throughout the research process, maintain accurate documentation, and assist with enrollment efforts. It is a strong opportunity for someone who enjoys patient-facing work, values detail and process, and wants to grow a career in clinical research.

RESPONSIBILITIES

Support clinical study start-up, patient visits, study conduct, and closeout activities Assist with recruiting, screening, scheduling, and following up with potential study participants Document patient assessments, observations, procedures, and test results in accordance with study requirements Help maintain accurate source records, electronic case report forms, study files, and supply documentation Support the informed-consent process and protect patient privacy and study confidentiality Communicate closely with coordinators, investigators, site leadership, and other study team members while promptly escalating safety concerns or adverse events

QUALIFICATIONS

Associate degree in a science-related field or comparable clinical research experience; bachelor's degree is preferred One to three years of experience in clinical research, biological research, healthcare, or a similar environment Familiarity with Good Clinical Practice, research regulations, and clinical trial workflows is preferred Phlebotomy experience required Strong communication skills and the ability to provide a professional, welcoming patient experience Organized, dependable, adaptable, and comfortable using Microsoft Office and general computer systems

Pay:

$20.00 - $30.00 per hour

Benefits:

401(k) 401(k) matching Dental insurance Employee assistance program Employee discount Flexible spending account Health insurance Health savings account Life insurance Paid time off Parental leave Referral program Tuition reimbursement Vision insurance

Experience:

Phlebotomy:

1 year (Required)

Work Location:

In person