Clinical Research Assistant - On-Site, Phlebotomy Preferred

SmartRecruiters, Inc.; Chattanooga (TN); On-site; USD 42,000 - 58,000; Full time

Benefits offered by this job

401(k)

Disability insurance

Employee assistance program

Flexible spending account

Health insurance

Life insurance

Paid time off

Vision insurance

Job summary

M3 Wake Research, an M3USA Company, is seeking a Clinical Research Assistant to support on-site clinical trials in Chattanooga, TN. You will work under the guidance of site leadership, PI, and CRC to ensure protocol compliance and high-quality data.

You will assist with phlebotomy, specimen handling, visit coordination, and regulatory filing while prioritizing participant safety and HIPAA compliance. The role requires careful attention to detail and strong teamwork in a fast-paced environment.

Qualifications

• At least 2 years of experience working in a healthcare setting.
• Phlebotomy experience is highly preferred.
• Previous experience as a medical assistant, EMT or LPN/LVN is encouraged.
• Familiarity with HIPAA guidelines and regulatory requirements is expected.

Responsibilities

• Maintain clinical supply inventory and monitor stock levels.
• Prepare participant charts, lab kits, requisitions and documentation for visits.
• Assist with phlebotomy, sample processing, and specimen shipment per protocol.
• Enter participant data accurately in source records and EDC systems.
• Support regulatory filings, study documentation, and archiving per GCP and SOPs.
• Collaborate with CRCs and clinical staff to ensure protocol adherence and safety.

Skills

Healthcare experience

Phlebotomy

EMT/MA/LPN/LVN background

Regulatory compliance

Communication & interpersonal skills

Job description

M3 Wake Research, an M3USA Company, is seeking a Clinical Research Assistant to support on-site clinical trials in Chattanooga, TN. You will work under the guidance of site leadership, PI, and CRC to ensure protocol compliance and high-quality data.

You will assist with phlebotomy, specimen handling, visit coordination, and regulatory filing while prioritizing participant safety and HIPAA compliance. The role requires careful attention to detail and strong teamwork in a fast-paced environment.