Research Assistant - Medical Lab Technician (Night Shift)

AMR Lexington; Knoxville (TN); On-site; USD 35,000 - 55,000; Full time

Benefits offered by this job

Night Shift Differential

Job summary

AMR Lexington in Knoxville, TN is seeking a Research Assistant - Medical Lab Technician for night shifts. This full-time role involves performing various administrative and clinical tasks to support study activities ensuring compliance with study protocols.

Key responsibilities include collecting clinical data, assisting in subject retention efforts, and maintaining study-related documentation. Valid MLT certification and phlebotomy skills are preferred.

Qualifications

• Must hold a valid MLT certification.
• Medical office experience is preferred.
• Phlebotomy skills preferred.

Responsibilities

• Perform administrative and clinical tasks in support of study activities.
• Ensure compliance with study protocols and regulatory guidelines.
• Collect clinical data such as vital signs and conduct subject interviews.

Skills

Valid MLT certification

Phlebotomy skills

Excellent attention to detail

Strong listening, verbal and written communication skills

Excellent task management and organizational skills

Ability to multi‑task

Education

Medical office experience or equivalent work experience

Job description

If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process.

Research Assistant - Medical Lab Technician (Night Shift)

Full Time Knoxville, TN, US

7 days ago Requisition ID: 1306

The role of the Research Assistant is responsible for performing a wide variety of administrative and clinical tasks to support the study site. The Research Assistant supports all study related activities to ensure that the study is completed accurately per study protocol. The Research Assistant is an integral role to assist with the flow of the clinic.

Wed, Thurs, Fri 6:30pm-7:00am OR Thurs, Fri, Sat from 6:30pm-7:00am

Shift differentials are dependent on schedule.

• United We Achieve
• Celebrate Diverse Perspectives
• Do the Right Thing
• Adapt and Persevere

The Research Assistant reports to the Site Manager/Team Lead.

Classification: Non-Exempt

Primary Responsibilities:

• Effectively prioritize tasks and meet deadlines in a fast‑paced environment.
• Maintain compliance responsibilities, including the identification and reporting of protocol deviations, serious adverse events (SAEs), and ensuring adherence to regulatory and site‑specific requirements.
• Monitor and report adverse events – recognize and promptly report AEs, protocol deviations, and safety concerns to the clinical team; document AE and SAE reporting in compliance with FDA, IRB, and sponsor requirements.
• Ensure compliance with study protocols and regulatory guidelines – adhere to Good Clinical Practice (GCP), FDA regulations, and site SOPs when conducting study‑related activities.
• Assist in subject retention efforts – support ongoing engagement, communication, and compliance to enhance subject retention throughout the study.
• Perform inventory management – track and manage study supplies, lab kits, and investigational products (if applicable) to ensure readiness for study visits.
• Assist in maintaining accurate, timely, and audit‑ready documentation of all study‑related activities.
• Perform laboratory responsibilities with accuracy – ensure proper labeling, handling, storage, and shipment of specimens per protocol and regulatory requirements.
• Apply strong problem‑solving skills and adapt to evolving study requirements.
• Handle confidential and sensitive information with discretion.
• Follow detailed instructions and maintain high levels of accuracy.
• Establish and maintain patient rapport during clinical drug trials, including management of subjects.
• Collect clinical data such as vital signs, EKGs, subject weights, diaries, etc.
• Retrieve and review medical records when required.
• Conduct subject interviews.
• Perform phlebotomy.
• File and pull study records.
• Answer and triage research office calls.
• Manage subject check‑in and check‑out processes.
• Prepare study materials, including screening packets, informed consents, and charts for the next business day.
• File study documents in the subject’s chart.
• Develop rapport with study sponsors, monitors, and participants.
• Assist the clinical team (CRCs, laboratory, data management, etc.) to complete study activities.
• Educate subjects on diaries as studies require.
• Maintain accurate and timely documentation.
• Perform unblinded duties as assigned.
• Work occasional weekend and/or overtime hours as required.
• Complete other duties as assigned.

Desired Skills and Qualifications:

• Valid MLT certification
• Medical office experience, medical certificate, or equivalent work experience preferred.
• Phlebotomy skills preferred.
• Excellent attention to detail.
• Strong listening, verbal and written communication skills.
• Excellent task management and organizational skills.
• Ability to multi‑task in an evolving fast‑paced environment.
• Proficient knowledge of operating office equipment and software.
• Ability to be ambulatory most of the workday.
• Ability to lift, transfer, push, and manipulate equipment and patients requiring strength, gross motor, and fine motor coordination.

AMR Clinical does not discriminate in employment on the basis of race, color, religion, sex (including pregnancy and gender identity), national origin, political affiliation, sexual orientation, marital status, disability, genetic information, age, retaliation, parental status, military service, or other non‑merit factor.

** This job description is intended to be a representative summary of the major responsibilities and accountabilities of the staff holding this position. The staff may be requested to perform job‑related tasks other than those stated in this description.