Clinical Research Assistant

Duties And Responsibilities

• Assists coordinators with patient visits including scheduling/tracking, data acquisition/data entry, procedures such as biopsies, administration of photodynamic therapy, adhesive lesional stripping, and related tasks.
• Affixes with routine data verification and quality control, ensuring data integrity and consistency with prescribed study protocol.
• Affixes with physicians with patient care and treatment, assisting with instruments, injections, and suture removal.
• Collections EKGs and vital signs.
• Affixes with clinical trials coordinator and principal investigator with initiation and maintenance of study protocols.
• Affixes with study visits per study protocol, inclusive of source document and case report form completion and submission.
• Performs laboratory duties and functions related to study protocols.
• Ensures clinical trial files are documented in accordance with company standard operating procedures, study protocol and Good Clinical Practice.
• Reviews exclusion/inclusion criteria with the Principal Investigator or Lead Coordinator to ensure subject eligibility.
• Processes blood, urine, and biopsy samples in accordance with study protocols and IATA/OSHA standards.
• Stocks and organizes medical supplies in exam rooms as needed. Notifies appropriate personnel when supplies are needed.
• Screens potential research participants and clinical patients for enrollment.
• Working knowledge, at minimum, of all applicable protocols. Some team members may be assigned as the primary coordinator for a specific protocol, and should therefore have in-depth knowledge of that protocol.
• Adheres to all safety policies and procedures in performing job duties and responsibilities while supporting a culture of high quality and great customer service.
• Performs other duties that may be necessary or in the best interest of the organization.