Clinical Research Assistant

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This range is provided by Medix

TM. Your actual pay will be based on your skills and experience—talk with your recruiter to learn more.

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

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.

• 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.

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.

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

$22/hr‑$32/hr ($45,000‑$66,000 Annual Salary) dependent on background and years of experience

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