Lab Coordinator

Socket.dev; Lexington (KY); On-site; USD 42,000 - 62,000; Full time

Job summary

AMR Clinical seeks a Lab Coordinator to support the clinical research team by ensuring timely and accurate lab activities per study protocol. Responsibilities include processing and shipping specimens, maintaining equipment logs, and assisting with remote and on-site monitor visits.

The role requires phlebotomy and lab processing experience, strict adherence to safety and biosafety standards, and the ability to work in a fast-paced environment. Some weekend/overtime may be necessary.

Qualifications

• Medical Laboratory Technology degree preferred.
• Phlebotomy experience required.
• Lab processing experience required.
• Familiarity with hazardous material handling and biosafety protocols.
• Excellent attention to detail and ability to manage multiple priorities.

Responsibilities

• Ensure Compliance with Regulatory & Safety Standards – Adhere to GCLP, ICH-GCP, FDA, IATA, and OSHA regulations when handling and processing specimens.
• Perform Quality Control Checks – Inspect sample processing, storage conditions, and lab documentation to ensure compliance.
• Troubleshoot Lab Processing Issues – Identify and resolve delays, equipment malfunctions, and protocol deviations.
• Support Sponsor & Monitor Requests – Assist with remote and on-site lab monitoring visits, including document retrieval and audits.
• Develop & Implement Lab Training Programs – Train new team members on lab protocols, safety measures, and compliance requirements.
• Collaborate with Study Teams to Optimize Workflows – Work with monitors, clinical staff, CRCs, and regulatory teams to improve lab processes.
• Draw labs and collect specimen per the study protocol.
• Process and store lab specimens per study protocol.
• Package lab specimens according to study protocol.
• Ship lab specimens per study protocol.
• Answer queries in a timely manner.
• Inventory lab supplies.
• Unpack and store supplies and study materials from sponsors.
• Maintain logs for refrigeratos and freezers (and required equipment).
• Ensure calibration is maintained on all equipment.
• Complete forms and study documents with accuracy.
• Clean and sanitize lab area daily.
• Remove subject identifying documents when assisting with remote monitoring.
• Assist clinical team with all study activities as needed (e.g., vitals, EKGs, phlebotomy).
• Maintain a safe work environment, meeting IATA and OSHA standards.
• Serve as a resource in lab to ensure protocols are followed.
• Occasional weekend and/or overtime may be required.
• Other duties as assigned.

Skills

Phlebotomy

Lab processing

Troubleshooting

Biosafety

Documentation

Safety

English fluency

Education

Medical Laboratory Technology degree

College graduate

Job description

The role of a Lab Coordinator assists all team members of the clinical research team. The Lab Coordinator is responsible for ensuring all lab activities are completed timely, accurately, and per study protocol. This position includes but not limited to processing lab samples, shipping lab samples per protocol specification and timeline.

To consistently embody AMR Clinical’s Core Values:

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

The Lab Coordinator reports to the Site Manager/Lab Manager.

Classification: Non-Exempt

Primary Responsibilities:

• Ensure Compliance with Regulatory & Safety Standards – Adhere to Good Clinical Laboratory Practices (GCLP), ICH-GCP, FDA, IATA, and OSHA regulations when handling and processing specimens.
• Perform Quality Control Checks – Regularly inspect sample processing, storage conditions, and lab documentation to ensure compliance and prevent deviations.
• Troubleshoot Lab Processing Issues – Identify and resolve sample processing delays, equipment malfunctions, and protocol deviations to prevent disruptions.
• Support Sponsor & Monitor Requests – Assist with remote and on-site lab monitoring visits, including document retrieval, sample reconciliation, and audit preparation.
• Develop & Implement Lab Training Programs – Train new team members on lab protocols, safety measures, and compliance requirements.
• Collaborate with Study Teams to Optimize Workflows – Work with monitors, clinical staff, CRCs, and regulatory teams to improve lab processes and efficiency.
• Draw labs and collect specimen per the study protocol
• Process and store lab specimens per study protocol
• Package lab specimens according to study protocol.
• Ship lab specimens per study protocol
• Answer queries in a timely manner
• Inventory lab supplies
• Unpack and put away supplies and study materials received from study sponsors.
• Maintain logs for refrigerator and freezers
• Maintain logs for required equipment
• Ensure calibration is maintained on all equipment
• Complete forms and study documents with accuracy
• Clean and sanitize lab area daily
• Remove subject identifying documents when assisting with remote monitoring activities.
• Assist clinical team with all study activities as needed. Such as vitals, EKG’s, phlebotomy, etc.
• Maintain a safe work environment, meeting IATA and OSHA standards.
• Serve as a resource in lab for all team members to ensure protocols are followed.
• Position may require occasional weekend and/or overtime hours.
• Other duties as assigned

Desired Skills and Qualifications:

• Medical Laboratory Technology degree preferred
• Phlebotomy experience required
• Lab processing experience required
• College graduate preferred
• Ability to troubleshoot lab equipment malfunctions and implement corrective actions.
• Familiarity with hazardous material handling and biosafety protocols.
• Excellent attention to detail, organizational skills, and ability to manage multiple priorities.
• Ability to function independently with little oversight
• Professional, highly motivated self-starter, and exercises initiative.
• Collaborative with a team mentality
• Ability to work fast-paced environment
• Organization and prioritization skills
• Excellent follow-up
• Ability to be ambulatory most of the workday.
• Ability to lift/transfer/push/manipulate equipment and patients, which requires strength, gross motor and fine motor coordination.
• Fluent in English.

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.