Clinical Research Assistant - 247992

Medix™; Los Angeles (CA); On-site; USD 45,000 - 66,000; Full time

Job summary

A healthcare organization in Los Angeles seeks a Clinical Research Assistant. This role involves supporting clinical research studies, maintaining data accuracy, and ensuring regulatory compliance. The ideal candidate should have an associate degree in a relevant field and 1-3 years of experience. Competitive hourly pay from $22 to $32, with direct hire employment.

Qualifications

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

Responsibilities

• Support clinical research activities and participant visits.
• Document participant data and test results following requirements.
• Obtain informed consent and ensure compliance with standards.
• Recruit and schedule eligible study participants.
• Maintain documentation and complete case report forms.
• Ensure confidentiality of study information.
• Report adverse events and deviations promptly.
• Assist with study material inventory.
• Communicate effectively with staff to support study progress.
• Participate in training to stay current with regulations.

Skills

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

Phlebotomy and ECG skills

Flexible and able to adapt to changing study needs

Education

Associate degree in a science-related field

Bachelor’s degree preferred

Job description

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Base pay range

$45,000.00/yr - $66,000.00/yr

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‑$32/hr ($45,000‑$66,000 Annual Salary) dependent on background and years of experience

Employment:

Direct Hire