Join our Team: Staff Positions

Department-Specific Responsibilities

• Assists in the conduct of clinical research studies or trials following established protocols and standard operating procedures; prepares and organizes space; sets up study-related equipment and supplies.
• Assists in the recruitment of Hispanic/ Latino participants through various methods including cold calls, individual solicitation, and attending various community outreach events.
• Sets up and monitors various research study protocols, such as data collection efforts.
• Assists with routine data collection to support clinical research (such as conducting interviews and symptom assessments).
• Schedules/calls subjects for appointments as directed; obtains screening information via phone or in person from script template for minimal risk studies; records and maintains screening/enrollment/master subject logs.
• Ensures proper recording and archival of all regulatory documents, including informed consent forms for submission to regulatory agencies, files all appropriate correspondence.
• Provides other various support for clinical research efforts (makes copies, prepares transmittal sheets for mailings, sends out various resources/information).

• Assists in the conduct of clinical research studies or trials following established protocols and standard operating procedures; prepares and organizes space; sets up study-related equipment and supplies.
• Sets up and monitors various research study protocols, such as data collection efforts.
• Assists with routine data collection to support clinical research (such as documenting vital signs, performing phlebotomy, etc.).
• Schedules/calls subjects for appointments as directed; obtains screening information via phone or in person from script template for minimal risk studies; records and maintains screening/enrollment/master subject logs.
• Ensures proper recording and archival of all regulatory documents, including informed consent forms for submission to regulatory agencies; files all appropriate correspondence
• Provides other various support for clinical research efforts (makes copies, prepares transmittal sheets for mailings, sends out various resources/information).

• Completes intervention training.
• Conducts in-person Occupational Therapy evaluation of people living with Mild Cognitive Impairment (MCI) and mild dementia (2 hours per client).
• Conducts 4-8 in-person sessions with virtual options (2 hours).
• Provides monitoring and support to persons living MCI and dementia, care partners, and outdoor professionals via telephone.
• Attends every other week virtual case conference meetings during the 12-week intervention.
• Completes post-intervention assessments and documentation.