Clinical Research Assistant-Cancer Center Protocol Office

GENERAL SUMMARY/ OVERVIEW STATEMENT:

The Clinical Research Assistant works under general supervision to perform administrative and clinical support for multiple clinical trials.

PRINCIPAL DUTIES AND RESPONSIBILITIES:

The following job duties will be performed under supervision by the Program Manager:

• Assists Clinical Research Coordinators with performing EKGs and vital signs
• Collects receipts and submits reimbursement for clinical trial participants
• Maintains kit inventories and clinical research supplies.
• Obtains outside records
• Assists with scanning of source documents
• Prepares research supplies for protocol visits
• Processes and ships blood and tissue samples per IATA guidelines
• Coordinate, obtain, process, and orders placed by the investigator and research team
• Provides administrative support duties

SKILLS/ ABILITIES/ COMPETENCIES REQUIRED:

• Careful attention to detail
• Good organizational skills
• Ability to follow directions
• Good verbal and written communication skills
• Computer literacy

EDUCATION:

• High School diploma preferred

EXPERIENCE:

• None

SUPERVISORY RESPONSIBILITY:

• None

WORKING CONDITIONS:

• Duties will be performed in a hybrid remote and office setting