On-Site Clinical Research Assistant — Chattanooga

M3 Wake Research; Chattanooga (TN); On-site; USD 42,000 - 65,000; Full time

Benefits offered by this job

401(k) with match

Dental insurance

Disability insurance

Employee assistance program

Flexible spending account

Health insurance

Life insurance

Paid time off

Vision insurance

Job summary

M3 Wake Research in Chattanooga, TN is seeking a Clinical Research Assistant to support daily trial activities under site leadership and the PI. The RA will help ensure protocol compliance, data quality, and participant safety through collaboration with clinical staff.

Responsibilities include managing supplies, assisting with phlebotomy and specimen handling, preparing visit materials, data entry, scheduling, and regulatory documentation in line with GCP and sponsor requirements.

Qualifications

• Experience in a healthcare setting with patient care focus.
• Phlebotomy experience preferred.
• Experience as medical assistant, EMT or LPN/LVN considered.
• Ability to maintain patient confidentiality per HIPAA.
• Excellent verbal and written communication.
• Strong attention to detail and ability to multitask.

Responsibilities

• Maintain clinical supply inventory and monitor stock levels.
• Keep exam rooms, labs, and equipment visit-ready; log maintenance.
• Assist with phlebotomy, sample processing, and specimen shipments.
• Prepare participant charts, lab kits, requisitions, and documentation.
• Perform protocol tasks (vital signs, ECGs, PFTs) as trained.
• Collect and enter data in source records and EDC; assist queries.
• Schedule participant visits and follow-ups; conduct reminders.
• Filing and archiving regulatory documents per GCP and sponsor rules.
• Collaborate with CRCs and staff to ensure protocol adherence.
• Complete required trainings (GCP, OSHA, IATA, SOPs).

Skills

Healthcare experience

Phlebotomy

MA/EMT/LPN

HIPAA knowledge

Communication skills

Detail-oriented

Multi-tasking

Job description

M3 Wake Research in Chattanooga, TN is seeking a Clinical Research Assistant to support daily trial activities under site leadership and the PI. The RA will help ensure protocol compliance, data quality, and participant safety through collaboration with clinical staff.

Responsibilities include managing supplies, assisting with phlebotomy and specimen handling, preparing visit materials, data entry, scheduling, and regulatory documentation in line with GCP and sponsor requirements.