Clinical Research Assistant

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.MAJOR RESPONSIBILITIES:Clinical OperationsAssist PI in development of protocol-specific tools to aid in study documentationCollect record, evaluate, update, and store/transport pertinent data and samples in relation to protocol Schedule patient tests and/or interviewsConduct patient telephone follow-upMaintain appropriate operations as needed including to stock, inventory, store, and order samples/supplies AdministrationReview medical records and medical record abstractions for consistency and completeness Comply with established policies, health and safety regulations and requirements, procedures, and department objectivesMaintain patient and study subject confidentialityREQUIRED QUALIFICATIONS:Bachelor’s degree or equivalent experienceExperience in using computer-based tools (Word, Excel, Access, Outlook, PowerPoint, etc.)Oral and written communication skillsExcellent organizational and interpersonal skills requiredPreferred Qualifications:Bachelor’s degree in psychology, neuroscience, biology, or a related fieldPrevious TMS or neurostimulation experience (preferred, but training available).Familiarity with clinical research protocols and regulatory compliance (preferred).Strong interpersonal and communication skills.Detail-oriented with excellent organizational and documentation abilities.Ability to work both independently and collaboratively in a multidisciplinary team.Current CPR certification (or ability to obtain).Physical Requirements:Ability to remain seated or standing for extended periods.Manual dexterity to handle TMS coils and related equipment.Occasional lifting (up to 25 lbs.) and movement of equipment.

Created: 2025-11-17