Clinical Research Coordinator (Medical Assistant)

The Client is seeking a Clinical Research Coordinator (Medical Assistant) for a full-time  contract-to-hire position supporting clinical research operations in Inglewood, CA. If you are passionate about patient care, clinical research, and supporting innovative medical studies, this role offers an excellent opportunity to contribute to high-quality clinical trials while advancing your healthcare career.

Pay: $27-33/hr

Location: Inglewood, CA

Overview
The Client supports the conduct of clinical research studies that advance medical knowledge and improve patient outcomes. In this role, the Clinical Research Coordinator (Medical Assistant) is responsible for coordinating study activities, interacting directly with study participants, and ensuring strict adherence to clinical protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines. This position plays a critical role in maintaining study integrity, data accuracy, and participant safety.

Schedule: Full-Time | Day Shift Onsite

Responsibilities:

• Communicate clearly and professionally with study participants regarding study objectives, visit schedules, and ongoing study instructions.
  

• Administer questionnaires and monitor participant compliance with study protocols.
  

• Respond promptly and appropriately to participant questions, concerns, and needs.
  

• Collect, review, and document patient medical history and current health conditions.
  

• Obtain and accurately document informed consent from study participants.
  

• Maintain accurate records related to study drug dispensation and accountability.
  

• Coordinate with clinical laboratories to ensure timely testing, processing, and reporting of results.
  

• Collect and assess information regarding concomitant medications.
  

• Review and evaluate medical records to ensure protocol compliance.
  

• Perform, assess, and document adverse events (AEs) and serious adverse events (SAEs).
  

• Conduct clinical procedures including EKGs, vital signs, nasal swabs, phlebotomy, and other protocol-specific assessments.
  

• Review and evaluate clinical laboratory reports for completeness and accuracy.
  

• Maintain up-to-date regulatory binders and research documentation for the site.
  

• Verify the accuracy, completeness, and quality of collected study data.
  

• Monitor and document temperature logs for investigational product (IP) storage.
  

• Support participant recruitment, screening, and ongoing engagement activities as needed.
  

• Develop and maintain electronic source (eSource) documentation in accordance with study protocols.
  

• Manage study startup documentation, training requirements, and timelines for assigned protocols.
  

• Ensure all protocol milestones, regulatory requirements, and study deadlines are consistently met.
  

• Adhere to all Client policies, procedures, and code of conduct.
  

• Maintain strict confidentiality and ensure compliance with all applicable regulatory and ethical standards.

Qualifications:

• Minimum of 1 year of experience with phlebotomy (certification required) and EKG procedures OR Medical Assistant certification.
  

• Associate’s degree in healthcare or a related field, or equivalent relevant experience.
  

• 2+ years of experience working with FDA regulations and Good Clinical Practice (GCP).
  

• Demonstrated analytical reasoning and problem-solving skills.
  

• Exceptional attention to detail with strong organizational abilities.
  

• Excellent verbal and written communication skills.
  

• Proven customer service skills with both internal teams and external stakeholders.
  

• Ability to manage multiple priorities effectively in a fast-paced clinical research setting.

What Happens Next:
Once you apply, you’ll move forward to the next steps if your skills and experience are a strong match. Even if this specific role is not the right fit, you’ll remain in the Client’s talent network—opening the door to future clinical and healthcare opportunities aligned with your background and career goals.

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