Under the direction of the Principal Investigator or designee, the Clinical Research Assistant is responsible for performing delegated tasks and procedures involving human subjects in support of clinical research protocols.
Responsibilities
MAJOR RESPONSIBILITIES:
Clinical Operations
Assist PI in development of protocol-specific tools to aid in study documentation
Collect record, evaluate, update, and store/transport pertinent data and samples in relation to protocol
Schedule patient tests and/or interviews
Conduct patient telephone follow-up
Maintain appropriate operations as needed including to stock, inventory, store, and order samples/supplies
Administration
Review medical records and medical record abstractions for consistency and completeness
Comply with established policies, health and safety regulations and requirements, procedures, and department objectives
Maintain patient and study subject confidentiality
Qualifications
REQUIRED QUALIFICATIONS:
Bachelor's degree or equivalent experience
Experience in using computer-based tools (Word, Excel, Access, Outlook, PowerPoint, etc.)
Oral and written communication skills
Excellent organizational and interpersonal skills required
