Clinical Research Medical Assistant

4 weeks ago


Los Angeles, California, United States Matrix Clinical Research Full time

Benefits:

401(k)

Competitive salary

Health insurance

Opportunity for advancement

Training & development

Matrix Clinical Research is a leading organization in the field of clinical research, dedicated to advancing medical knowledge and improving patient outcomes. We conduct cutting-edge research studies in various therapeutic areas, and we are looking for a dedicated Clinical Research Medical Assistant to join our dynamic team.

Job Summary:

The Clinical Research Medical Assistant will assist in the conduct of clinical trials by providing support to the clinical research team, ensuring the safety and well-being of study participants, and maintaining the integrity of study data. The ideal candidate is a detail-oriented professional with a passion for clinical research and patient care.

Key Responsibilities:

Assist in the recruitment, screening, and enrollment of study participants.

Perform vital signs, ECGs, phlebotomy, and other clinical procedures as required by study protocols.

Collect and process biological samples (e.g., blood, urine) for laboratory analysis.

Document patient visits and study procedures accurately in electronic medical records and case report forms.

Schedule and coordinate study visits and follow-ups.

Educate study participants about study protocols, procedures, and consent forms.

Monitor and report any adverse events or protocol deviations to the study coordinator.

Maintain inventory of study supplies and ensure that all equipment is in good working order.

Assist with data entry, filing, and organization of study documents.

Comply with Good Clinical Practice (GCP) guidelines and company SOPs.

Work collaboratively with the research team to ensure the smooth running of clinical trials.

Qualifications:

Certified Medical Assistant (CMA) or equivalent certification.

Experience in a clinical research setting preferred.

Knowledge of medical terminology and clinical procedures.

Strong organizational and time-management skills.

Excellent communication and interpersonal skills.

Ability to work independently and as part of a team.

Proficient in Microsoft Office and electronic medical records systems.

CPR certification required.

Benefits:

Competitive salary and benefits package.

Opportunities for professional development and growth.

Collaborative and supportive work environment.

Contribution to impactful clinical research that improves patient lives.


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