Clinical Research Coordinator

SQRL; Murrieta (CA); On-site; USD 70,000 - 79,000; Full time

Benefits offered by this job

401k w/match

15 days PTO

Consistent schedule, no overnights or weekends

Job summary

A leading clinical research organization based in Murrieta, California, is looking for an Associate Director of Recruiting to support oncology clinical trials. This full-time position requires 2+ years of CRC experience, phlebotomy skills, and on-site work. Candidates will engage in vital signs, patient recruitment, and overall study coordination. A competitive salary of $70,000 - $79,000 and great benefits are offered.

Qualifications

• 2+ years of experience working as a CRC on sponsor-backed clinical trials.
• Phlebotomy and lab processing experience.
• Ability to work on site M-F; no remote or hybrid days.

Responsibilities

• Conduct vital signs, blood draws, EKGs, and scans.
• Manage patient recruitment, enrollment, and consent.
• Coordinate the study from start up to close out.

Skills

Clinical trial coordination

Patient recruitment

Data management

Phlebotomy

Job description

Associate Director of Recruiting at SQRL | Clinical Research, Healthcare, Biotech, Life Sciences

Highlights

• $70,000 - $79,000 annual salary based on experience
• Great benefits including 401k w/match and 15 days PTO
• Consistent schedule, no overnights or weekends
• Work with cutting edge oncology research trials

About Our Client

Our client is a fast growing site network that currently has over 30 sites and constantly expanding! They focus on diversity in their trials including therapeutic areas: oncology, cardiology, metabolic disorders, renal, CNS, pulmonology, and vaccines. Their sites conduct studies spanning Phases I-IV and they've been awarded for excellence in recruitment and recognized in the industry for retention, a best‑in‑class experience for patients and sponsors.

Responsibilities

As a CRC you will be a specialized research professional under the direction of the clinical Principal Investigator and Site Manager. While the PI and Site Manager are responsible for the overall design, conduct, and management of the clinical trial, you support, facilitate, and coordinate the daily clinical trial activities and play a critical role in the conduct of the study including supporting patients throughout the clinical trial process!

• Conduct procedures such as vital signs, blood draws, EKGs, and scans.
• Patient recruitment, enrollment, scheduling, and consent
• Lab procedures and shipments
• Maintain GCP and follow protocols
• Data management in EDC systems
• Overall coordination of the study from start up to close out
• Focus on oncology based research studies

Qualifications:

• 2+ years of experience working as a CRC on sponsor-backed clinical trials
• Phlebotomy and lab processing experience (ability to perform without supervision)
• Ability to work on site M-F on site (there is no remote or hybrid days)
• Experience working with Oncology clinical trials

Seniority level

• Associate

Employment type

• Full-time

Job function

• Research
• Research Services