• Scheduling
• Data Entry
• Patient Recruitment
• Scanning
• Faxing
• Reminder Calls
• Possess a sound and in-depth understanding of each protocol’s lab requirements.
• Review each laboratory manual for study related procedures.
• Prepare and set up appropriate laboratory kit for each subject.
• Confirm subject identifiers on lab tubes and requisitions are correct.
• Perform blood draws (if qualified), collect urine specimens, process, store, and ship research specimens as mandated by the protocol.
• Complete sample and shipping tracking logs, if required.
• Order dry ice and track invoices.
• Ensure adequate supply of lab kits and shipping supplies for each study is maintained at all times.
• Destroy expired lab kits, dispose of excess shipping supplies.
• Record daily temperatures.
• Perform timely, accurate electronic data entry, using the protocol-specific eCRF completion guidelines.
• Verify entries for accuracy and completeness.
• Respond to automatic system-generated queries.
• Relay all other queries to appropriate study coordinator.
• Conduct memory assessments.

QUALIFICATIONS:

• 
  Bachelor’s Degree
• Two years of relevant experience or an equivalent combination of education and training is an asset
• Phlebotomy Training
• 2 or more years experience with working in a certified lab environment

REQUIRED KNOWLEDGE, SKILLS, ABILITIES:

• 
  Computer literacy required
  
• Proficient in MS Office required