Inglewood, California, United States · On-site
$28/hr–$30/hr
*This is a full-time, temporary position currently estimated to last until December 31, 2026 (subject to business needs). There may be the possibility for this position to become permanent.* Summary: The Clinical Researc…
Skills: Clinical Research Coordination, Participant Screening, Informed Consent, Data Collection, Medical Terminology
Dallas, Texas, United States · On-site
*This is a full-time, temporary position currently estimated to last until December 31, 2026 (subject to business needs). There may be the possibility for this position to become permanent.* Summary: The Clinical Researc…
Skills: Clinical Research Coordination, Participant Screening, Informed Consent, Data Collection, Medical Terminology
Las Vegas, Nevada, United States · On-site
*This is a full-time, temporary position currently estimated to last until December 31, 2026 (subject to business needs). There may be the possibility for this position to become permanent.* Summary: The Clinical Researc…
Skills: Clinical Research Coordination, Participant Screening, Informed Consent, Data Collection, Medical Terminology
Los Angeles, California, United States · On-site
$28/hr–$30/hr
*This is a full-time, temporary position currently estimated to last until December 31, 2026 (subject to business needs). There may be the possibility for this position to become permanent.* Summary: The Clinical Researc…
Skills: Clinical Research Coordination, Participant Screening, Informed Consent, Data Collection, Medical Terminology
San Diego, California, United States · On-site
$28/hr–$30/hr
*This is a full-time, temporary position currently estimated to last until December 31, 2026 (subject to business needs). There may be the possibility for this position to become permanent.* Summary: The Clinical Researc…
Skills: Clinical Research Coordination, Participant Screening, Informed Consent, Data Collection, Medical Terminology
Rochester, New York, United States · On-site
$28/hr–$30/hr
*This is a full-time, temporary position currently estimated to last until December 31, 2026 (subject to business needs). There may be the possibility for this position to become permanent.* Summary: The Clinical Researc…
Skills: Clinical Research Coordination, Participant Screening, Informed Consent, Data Collection, Medical Terminology
Media, Pennsylvania, United States · On-site
*This is a full-time, temporary position currently estimated to last until December 31, 2026 (subject to business needs). There may be the possibility for this position to become permanent.* Summary: The Clinical Researc…
Skills: Clinical Research Coordination, Participant Screening, Informed Consent, Data Collection, Medical Terminology
New Port Richey, Florida, United States · On-site
*This is a full-time, temporary position currently estimated to last until December 31, 2026 (subject to business needs). There may be the possibility for this position to become permanent.* Summary: The Clinical Researc…
Skills: Clinical Research Coordination, Participant Screening, Informed Consent, Data Collection, Medical Terminology
Buffalo, New York, United States · On-site
$28/hr–$30/hr
*This is a full-time, temporary position currently estimated to last until December 31, 2026 (subject to business needs). There may be the possibility for this position to become permanent.* Summary: The Clinical Researc…
Skills: Clinical Research Coordination, Participant Screening, Informed Consent, Data Collection, Medical Terminology
Houston, Texas, United States · On-site
$90k–$120k/yr
About the Role: The Clinical Operations Manager is responsible for daily clinic operations, administrative functions, and the management of office personnel. This role acts as a liaison between patients, medical staff, c…
Skills: Clinic Operations Management, Clinical Research Coordination, Budget Management, Patient Recruitment, Regulatory Compliance
San Diego, California, United States · On-site
$22/hr–$26/hr
About the Company: We’re people with a purpose, dedicated to advancing medical innovation and healing technology through groundbreaking research, diligent patient care and strong executive management. Our hands-on …
Skills: Phlebotomy, Lab Maintenance, Data Recording, Equipment Calibration, Sample Storage
Rochester, New York, United States · On-site
$20/hr–$22/hr
Summary: The Clinical Research Assistant supports the conduct of clinical trials by performing protocol-required procedures, coordinating study activities, and engaging directly with study participants. This role is resp…
Skills: Clinical Trial Coordination, Patient Recruitment, Informed Consent, Phlebotomy, EKG
On-site
About the Role: The Clinical Research Coordinator (CRC) supports the conduct of clinical trials by coordinating study visits, managing data collection, and ensuring compliance with protocols and regulatory guidelines. Th…
Skills: Clinical Trial Coordination, Data Collection, Regulatory Compliance, Good Clinical Practice, Patient Monitoring
Inglewood, California, United States · On-site
$120k–$148k/yr
About the Role: The Clinical Operations Manager is responsible for daily clinic operations, administrative functions, and the management of office personnel. This role acts as a liaison between patients, medical staff, c…
Skills: Clinical Operations Management, Personnel Training, Budget Management, Patient Recruitment, Regulatory Compliance
On-site
Summary: The Director, Site Performance is responsible for improving operational performance across Alliance Clinical Network's portfolio of research sites. This role serves as a strategic partner to the Vice President o…
Skills: Clinical Research Operations, Site Performance Management, Patient Recruitment, Operational Assessment, KPI Analysis
Los Angeles, California, United States · On-site
$20/hr–$26/hr
About this Role: The Assistant Clinical Research Coordinator (ACRC) supports the planning, coordination, and execution of clinical research studies within a healthcare setting. This role ensures clinical trials are condu…
Skills: Participant Recruitment, Data Collection, Clinical Trial Coordination, Phlebotomy, Regulatory Documentation
Inglewood, California, United States · On-site
$27/hr–$33/hr
About the Role: The Clinical Research Coordinator (CRC) supports the conduct of clinical trials by coordinating study visits, managing data collection, and ensuring compliance with protocols and regulatory guidelines. Th…
Skills: Phlebotomy, EKG Procedures, Clinical Trial Coordination, Data Collection, Regulatory Compliance
Inglewood, California, United States · On-site
$20/hr–$26/hr
About this Role: The Assistant Clinical Research Coordinator (ACRC) supports the planning, coordination, and execution of clinical research studies within a healthcare setting. This role ensures clinical trials are condu…
Skills: Clinical Research Coordination, Participant Recruitment, Data Collection, Phlebotomy, Regulatory Documentation
Inglewood, California, United States • On-site
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The Clinical Research Coordinator supports the execution of clinical trials by managing participant screening, enrollment, and data collection. They ensure all study activities comply with protocols, regulatory requirements, and institutional policies to maintain data integrity and participant safety.
A high school diploma is required, though an associate's degree in a health-related field and medical assistant certification are preferred. Candidates must have experience in patient care and medical terminology, with a strong preference for knowledge of GCP and FDA regulations.
This is a full-time, temporary position currently estimated to last until December 31, 2026 (subject to business needs). There may be the possibility for this position to become permanent.
Summary:
The Clinical Research Coordinator (CRC) supports the coordination and execution of clinical research studies within a healthcare setting. This role ensures clinical trials are conducted in compliance with study protocols, regulatory requirements, and institutional policies while protecting participant safety and data integrity. Working closely with Principal Investigators (PIs), research staff, and study participants, the CRC assists with participant screening, data collection, and the coordination of study activities to ensure accuracy, efficiency, and high-quality research outcomes.
Essential Duties and Responsibilities:
Qualifications:
Certificates, Licenses, and Registrations:
ACN does not provide visa sponsorship for this role. Candidates who will require immigration or visa sponsorship at any time now or in the future (including, but not limited to, H‑1B, TN, or STEM OPT training plans) are not eligible for this role.
About the Company:
At Alliance Clinical Network, our mission is to advance medical research by enrolling diverse populations in high-quality clinical trials. We are committed to maintaining the highest standards of integrity and excellence, and to ensuring that every participant receives respectful and compassionate care. We strive to build a tightly knit, supportive and collaborative environment where our team members can thrive and make meaningful contributions to human health.
Alliance Clinical Network Helps Advance Breakthrough Medical Treatments for All
For more than a decade, Alliance Clinical Network's fully integrated, wholly owned and operated clinical research sites have helped advance human health by delivering exceptional clinical trial data gathered from a proprietary, ready-to-tap, group of >250,000 diverse participants. We bring our sponsors and partner CROs three key advantages: * Expedited study startup and rapid enrollment * Comprehensive focus on quality for reliable, audit-ready data * 85% of participant population drawn from underrepresented groups While each of our eight sites is affiliated with a local hospital, our centralized management standardizes processes and technology across them all. That maximizes efficiency, enhances quality, and ensures consistent study execution. It also creates a solid foundation from which to easily scale to meet study needs.
Offices: 601 State St, Southlake, Texas 76092, US
Alliance Clinical Network Helps Advance Breakthrough Medical Treatments for All
For more than a decade, Alliance Clinical Network's fully integrated, wholly owned and operated clinical research sites have helped advance human health by delivering exceptional clinical trial data gathered from a proprietary, ready-to-tap, group of >250,000 diverse participants. We bring our sponsors and partner CROs three key advantages: * Expedited study startup and rapid enrollment * Comprehensive focus on quality for reliable, audit-ready data * 85% of participant population drawn from underrepresented groups While each of our eight sites is affiliated with a local hospital, our centralized management standardizes processes and technology across them all. That maximizes efficiency, enhances quality, and ensures consistent study execution. It also creates a solid foundation from which to easily scale to meet study needs.
Offices: 601 State St, Southlake, Texas 76092, US
