Clinical Research Lab Technician (Contract) - Part-Time

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

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