Clinical Research Assistant

Get AI-powered advice on this job and more exclusive features. This range is provided by MedixTM. Your actual pay will be based on your skills and experience—talk with your recruiter to learn more. 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 #J-18808-Ljbffr