Laboratory Tech (Contract)

Accelerated Clinical Trials; Oregon (WI); On-site; USD 24,796 - 44,083; Part time

Job summary

Accelerated Clinical Trials is seeking a detail-oriented Clinical Research Laboratory Technician (Contract) to support clinical trials and biospecimen-related research activities. This role emphasizes high-quality sample handling, proper documentation, and strict compliance with regulatory standards in a clinical research setting.

Responsibilities include processing and labeling samples, maintaining logs and chain-of-custody, shipping specimens to central labs, instrument maintenance, assisting

Qualifications

• High school diploma or equivalent (required).
• Basic laboratory experience (academic or professional).
• Preferred: Bachelor’s degree in science with specimen processing/shipping experience.
• Strong understanding of biospecimen handling, safety, and sterile technique.

Responsibilities

• Process, aliquot, centrifuge, label, and store trial samples per study protocols.
• Maintain logs and chain-of-custody with GMP/GCP compliance.
• Prepare and ship samples to central labs with correct packaging and temperature controls.
• Maintain lab instruments (centrifuges, refrigerators, freezers, pipettes).
• Assist clinical research coordinators with specimen collection setup and visit preparation.
• Track supplies and inventory for ongoing studies.
• Participate in site audits, monitoring visits, and quality control activities.
• Follow all site SOPs, safety protocols, and regulatory requirements.

Skills

Biospecimen handling

Documentation

Sterile technique

Regulated environment

Education

High school diploma or equivalent

Bachelor’s degree in science

Job description

Job Title

Clinical Research Laboratory Technician (Contract)

Job Status

Part-time or PRN

Department

Clinical Research

Reports To

Nurse Manager/Clinical Research Manager

Location

Snellville, GA

Job Summary

We’re seeking a detail-oriented Clinical Research Laboratory Technician (Contract) to support clinical trials and biospecimen-related research activities. This role is essential in ensuring high-quality sample handling, proper documentation, and compliance with regulatory standards within a clinical research setting.

Key Responsibilities

• Perform laboratory procedures related to clinical trial samples, including processing, aliquoting, centrifugation, labeling, and storage according to study protocols.
• Maintain accurate and complete sample logs, chain-of-custody documentation, and lab records in compliance with GCP/ICH guidelines.
• Prepare and ship biological samples (e.g., blood, urine, swabs) to central labs using appropriate packaging and temperature controls.
• Maintain laboratory instruments (centrifuges, refrigerators, freezers, pipettes, etc.).
• Assist clinical research coordinators with specimen collection setup and visit preparation.
• Track and manage lab supplies, kits, and inventory for ongoing studies.
• Participate in site audits, monitoring visits, and quality control activities.
• Follow all site SOPs, safety protocols, and regulatory requirements.

Qualifications

• High school diploma or equivalent (required)
• Basic laboratory experience (academic or professional).
• Strong understanding of biospecimen handling, safety, and sterile technique.
• Excellent documentation skills and attention to detail.
• Ability to work in a fast-paced, regulated environment.
• Preferred qualifications: Bachelor’s degree in science with previous experience in specimen processing and shipping

Working Conditions

• Work performed in a clinical and laboratory environment with routine exposure to biological specimens.
• Occasional early morning/late evening sample processing may be required based on study visit times.