Clinical Research Assistant - 254830

Medix™; Los Angeles (CA); On-site; USD 22,000 - 30,000; Full time

Job summary

Medix™ is seeking a Clinical Research Assistant in Los Angeles, CA to support the planning and execution of clinical research studies. This role involves assisting with study start-up, documentation, and recruitment while adhering to Good Clinical Practice (GCP) and regulatory requirements.

The ideal candidate will have an associate degree in a science-related field and prefer 1-3 years of relevant experience. This position offers a pay range of $22 to $30 per hour, dependent on experience, and is onsite five days a week.

Qualifications

• 1–3 years of experience in clinical or biological research preferred.
• Equivalent clinical or biological research experience may be considered.

Responsibilities

• Support clinical research activities, including scheduling participant visits.
• Accurately document participant data and test results.
• Assist with obtaining informed consent and ensuring compliance.
• Recruit and schedule eligible study participants to meet enrollment goals.
• Maintain accurate source documentation and complete case report forms.

Skills

Knowledge of clinical research procedures and GCP guidelines

Strong communication skills

Organizational skills

Documentation skills

Proficiency with Microsoft Office 365

Detail-oriented

Phlebotomy skills

ECG skills

Adaptability

Education

Associate degree in a science-related field

Bachelor’s degree

Tools

Electronic data systems

Job description

Clinical Research Assistant in Los Angeles, CA (90067)

Summary

The Research Assistant I supports the planning, coordination, and execution of clinical research studies under the direct supervision of the Site Director or Clinical Research Coordinator (CRC). This role assists with study start‑up, conduct, and close‑out activities to ensure accurate data collection and regulatory compliance in accordance with Good Clinical Practice (GCP), Institutional Review Board (IRB) requirements, and sponsor protocols.

Responsibilities

• Support clinical research activities, including scheduling and conducting participant visits according to study protocols.
• Accurately document participant data, test results, and observations following regulatory and protocol requirements.
• Assist with obtaining informed consent and ensuring compliance with IRB and GCP standards.
• Recruit, screen, and schedule eligible study participants to meet enrollment goals.
• Maintain accurate source documentation and complete case report forms (CRFs).
• Ensure confidentiality of all participant and study information.
• Report adverse events and protocol deviations promptly to supervising staff.
• Assist with study material inventory, including investigational products and lab supplies.
• Communicate effectively with investigators, sponsors, and site staff to support study progress.
• Participate in ongoing training to stay current with research regulations and best practices.
• Perform additional duties as assigned.

Qualifications

Education:

• Associate degree in a science‑related field required; Bachelor’s degree preferred.
• Equivalent clinical or biological research experience may be considered.

Experience:

• 1–3 years of experience in clinical or biological research preferred.

Skills and Competencies:

• Knowledge of clinical research procedures and GCP guidelines.
• Strong communication, organizational, and documentation skills.
• Proficiency with Microsoft Office 365 and electronic data systems.
• Detail‑oriented, ethical, and professional in all interactions.
• Phlebotomy and ECG skills preferred.
• Flexible and able to adapt to changing study needs.

Hours: Monday‑Friday; Normal Business Hours; Onsite 5 Days a Week

Pay: $22/hr-$30/hr ($45,000-$62,400 Annual Salary) - Dependent on background and years of experience