• Conduct clinical studies according to all regulations and guidelines

• Ensure the safety and welfare of the study participants.
• Follow requirements for reporting and study approval

• Ability to read, understand and perform research protocols to ensure all study activities are completed accurately and completely
• Recruit and screen potential study participants according to the protocol’s inclusion and exclusion criteria
• Effectively interact with Principal Investigator, monitor and staff .
• Collect, process and document subject blood samples, cultures, tissues and other specimens for laboratory analysis.
• Maintain detailed, accurate and complete records
• Medical Terminology Knowledge/Experience
• Detail-oriented with the ability to collect, compile and analyze study information.
• Ability to work independently on multiple tasks and manage time effectively.
• Ability to work with Study Research Team and support other Study Coordinators and site staff as needed
• Must be a LPN, Medical Assistant, Phlebotomist or comparative experience in Research, medical or health-related field.
• Must have one year experience in a health or research environment, familiarity with basic medical and research terminology and procedures.

Job Type: Full-time

Pay: $13.00 - $16.00 per hour

Benefits:

• 401(k)
• Dental insurance
• Health insurance
• Paid time off
• Vision insurance

Schedule:

• 8 hour shift

Work Location: One location

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