Research Assistant / Certified Medical Assistant

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

Job summary

Alliance Clinical Network is seeking a Research Assistant / Certified Medical Assistant to support clinical studies at West Hills, CA. The role combines patient care with study coordination under the supervision of the PI and senior staff.

Responsibilities include participant screening, data collection, scheduling visits, document handling, and adhering to GCP, HIPAA, and study protocol requirements, with emphasis on accuracy and patient safety.

Qualifications

• Medical Assistant certification required; injections/vaccinations performed.
• High school diploma or equivalent; associates degree preferred in health field.
• Knowledge of clinical research basics and healthcare settings.
• Strong organization and time-management; able to handle multiple priorities.
• Clear, professional communication with diverse populations.

Responsibilities

• Coordinate and execute clinical research protocols under supervision.
• Perform injections and vaccinations on patients in trials.
• Recruit, screen, and enroll study participants per protocol.
• Schedule visits, procedures and follow-ups with participants and teams.
• Collect, record, and maintain accurate research data and source docs.
• Communicate with participants; support adherence to study requirements.
• Monitor progress and report adverse events or deviations to the team.
• Assist with regulatory documents; aid audits and inspections as needed.
• Follow SOPs and Good Clinical Practice guidelines.
• Handle laboratory specimens per regulations and ship them appropriately.
• Maintain organized study records and documentation.
• Apply critical thinking to support study operations and problem resolution.
• Perform other duties as assigned.

Skills

Medical Assistant certification

Organizational skills

Communication with diverse populations

Team collaboration

Attention to detail

Education

High school diploma or equivalent

Associate degree in health-related field

Tools

Electronic data capture systems

Clinical trial management software

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.

Research Assistant / Certified Medical Assistant

FullTime Professional Alliance Clinical West Hills, West Hills, CA, US

20 days ago Requisition ID: 1332

Salary Range: $20.00 To $26.00 Hourly

Summary:

The Assistant Clinical Research Coordinator I (ACRC I) 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 I 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.


• Perform injections and/or vaccinations on patients in various clinical research trials


• 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:

• Medical Assistant (MA) certification required (This role involves performing injections/vaccinations.)


• 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.


• 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.

Certificates, Licenses, and Registrations:

• Medical Assistant (MA) certification required.


• Current CPR/BLS certification preferred.


• Certification as a Clinical Research Coordinator (e.g., CCRC) or a willingness to obtain certification 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.

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.