Research Assistant - (Night Shift)

About the role

Research Assistant supports clinical trial site activities including clinical data collection, phlebotomy, lab processing, and GCP/FDA-compliant documentation on night shifts.

Requirements

• Valid MLT certification
• Lab processing skills required
• Medical office experience or medical certificate preferred
• Phlebotomy preferred
• Attention to detail
• Ability to lift/transfer patients

What you'll do

• Clinical drug trial subject management
• Vitals, EKG, phlebotomy
• Adverse event and protocol deviation reporting
• Specimen handling and shipment
• Study documentation and ICF logs

Where this was posted

• Indeed

  last seen 1h ago
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