Clinical Research Assistant

Overview GENERAL SUMMARY OF POSITION:  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