Clinical Research Assistant

Summary
Assist research coordinator with specimen collections and data management for clinical trials.
Essential Duties and Responsibilities
Screen and enroll participants for clinical trials based on their eligibility status
Provide informed consent to patients after explaining the details of the trials
Collect and test biological samples (nasal swabs, nasal pharyngeal swabs, etc.)
Ensure that samples are collected, processed, stored, and shipped per protocol and in accordance with FDA standards.
Answer patients' questions regarding the protocols in a clear and concise manner
Ensure all documentation is complete, thorough, and submitted in a timely manner
Assist in training other research and lab personnel on study procedures as directed
Maintain competency as testing personnel to assist with clinic workflow as volume dictates
Must be adaptable and willing to train on new protocols as they become available
Must be detail-oriented and reliable.
Other Duties and Responsibilities
Responds promptly to study coordinator's needs and the needs of the Primary Investigator.
Treats people with respect, inspires the trust of others, and works with integrity.
Adapts to changes in the work environment, manages competing demands.
Other duties and responsibilities as assigned.
Qualifications
Previous laboratory experience required.
Previous research experience preferred.
Work Environment
Standing for long periods regularly
Occasionally required to sit, climb, balance, stoop, kneel, crouch, or crawl
Must regularly lift and/or move up to 10 pounds
Potential exposure to moving mechanical parts, fumes, or airborne particles

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