Assistant Clinical Research Coordinator

Alliance Clinical; Inglewood (CA); On-site; USD 28,000 - 36,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

401k

Job summary

Alliance Clinical Network is seeking an Assistant Clinical Research Coordinator to support planning, coordination, and execution of clinical studies in a healthcare setting. The role involves participant screening, data collection, and coordinating study activities to ensure accuracy and compliance with protocols.

You will work closely with Principal Investigators, research staff, and participants, ensuring safety, data integrity, and timely regulatory submissions.

Qualifications

• High school diploma or equivalent required; associate degree or higher in a health-related field preferred.
• Basic knowledge of clinical research principles, medical terminology, and healthcare environments.
• Strong organizational, time management, and attention-to-detail skills with the ability to manage multiple priorities.
• Ability to communicate clearly and professionally with diverse populations.
• Ability to work collaboratively in a fast-paced, team-oriented environment.
• Experience in clinical research or healthcare settings preferred.
• Knowledge of GCP, HIPAA, ALCOA principles, FDA regulations, and IATA guidelines preferred.
• Experience with participant recruitment, screening, and the informed consent process preferred.
• Proficiency with electronic data capture systems, clinical trial management software, and Microsoft Office (Excel, Word, and PowerPoint) preferred.

Responsibilities

• Assist in coordination and execution of clinical research protocols under supervision.
• Recruit, screen, and enroll study participants per protocol requirements and ethics guidelines.
• Coordinate and schedule study visits, procedures, and follow-up activities with participants and clinical teams.
• Collect, record, and maintain accurate clinical research data and source documentation.
• Communicate with participants to provide education and support adherence to study requirements.
• Monitor study progress and report adverse events and protocol deviations to the team.
• Support preparation, maintenance, and submission of regulatory documents; assist with audits and inspections.
• Adhere to SOPs and Good Clinical Practice (GCP) guidelines.
• Draw, process, and ship laboratory specimens per regulations.
• Scan, upload, file, and maintain organized study records.
• Apply critical thinking to support efficient study operations and problem resolution.
• Perform other duties as assigned.

Skills

Clinical research basics

Data collection

Regulatory compliance

Communication with participants

Team collaboration

Microsoft Office

GCP knowledge

HIPAA knowledge

Education

Associate degree or higher preferred

High school diploma or equivalent

Tools

EDC systems

CTMS

Microsoft Office

Job description

If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process.

Assistant Clinical Research Coordinator

FullTime Professional Los Angeles, Inglewood, CA, US

30+ days ago Requisition ID: 1288

Salary Range: $20.00 To $26.00 Hourly

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 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 ACRC 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:

• Assist in the coordination and execution of clinical research protocols under the supervision of the PI and senior research staff.
• Recruit, screen, and enroll study participants in accordance with protocol requirements and ethical guidelines.
• Coordinate and schedule study visits, procedures, and follow-up activities with study participants and clinical teams.
• Collect, record, and maintain accurate clinical research data and source documentation in compliance with regulatory and institutional standards.
• Communicate with study participants to provide education, answer questions, and support adherence to study requirements.
• Monitor study progress and report adverse events, protocol deviations, and other study-related issues to the research team.
• Support the preparation, maintenance, and submission of regulatory documents; assist with audits and inspections as needed.
• Adhere to site standard operating procedures (SOPs) and Good Clinical Practice (GCP) guidelines.
• Draw, process, and ship laboratory specimens, including the handling of dangerous goods, in accordance with regulations.
• Scan, upload, file, and maintain organized study records and documentation.
• Apply critical thinking skills to support efficient study operations and problem resolution.
• Perform other duties as assigned.

Qualifications:

• High school diploma or equivalent required; an associate’s degree or higher in a health-related field preferred.
• Basic knowledge of clinical research principles, medical terminology, and healthcare environments.
• Strong organizational, time management, and attention-to-detail skills with the ability to manage multiple priorities.
• Ability to communicate clearly and professionally with diverse populations.
• Ability to work collaboratively in a fast-paced, team-oriented environment.
• Experience in clinical research or healthcare settings preferred.
• Knowledge of GCP, HIPAA, ALCOA principles, FDA regulations, and IATA guidelines preferred.
• Experience with participant recruitment, screening, and the informed consent process preferred.
• Proficiency with electronic data capture systems, clinical trial management software, and Microsoft Office (Excel, Word, and PowerPoint) preferred.

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.

Certificates, Licenses, and Registrations:

• Certified Medical Assistant (MA) or Phlebotomist.
• Current CPR/BLS certification preferred.
• Certification as a Clinical Research Coordinator (e.g., CCRC) or a willingness to obtain certification preferred.

Benefits: Medical, Dental, Vision, 401k, PTO and more!

Location: Monday - Friday / on-site / Inglewood, CA

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.