Clinical Research Assistant 253578
Behavioral Health Market Context
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Job Description
• Creating and maintaining patient charts for all assigned studies.
• Preparing participant visits based on CRC's schedule, ensuring all source documents, assessments, lab kits, and other visit materials are available and accurate. Filing of lab results, EKG results, and other communication in designated patient charts.
• Maintaining inventory of study-specific supplies, including lab kits, assessments, and participant-facing materials.
• Timely completion of data entry and query resolution for all CRFs, based on sponsor-specific timelines and deadlines established in contract or other communication.
• Assisting Coordinators in assessments, including but not limited to blood pressure, urine collection.
• Communicating with study participants, caregivers, third-party vendors, and laboratories as needed.
• Assisting Coordinators with scheduling, copying, faxing, and other clerical tasks.
• Aiding Coordinators in the facilitation of study monitoring visits.
• Completion of daily responsibilities delegated by CRC as they pertain to the study and/or participants.
• Preparing participant visits based on CRC's schedule, ensuring all source documents, assessments, lab kits, and other visit materials are available and accurate. Filing of lab results, EKG results, and other communication in designated patient charts.
• Maintaining inventory of study-specific supplies, including lab kits, assessments, and participant-facing materials.
• Timely completion of data entry and query resolution for all CRFs, based on sponsor-specific timelines and deadlines established in contract or other communication.
• Assisting Coordinators in assessments, including but not limited to blood pressure, urine collection.
• Communicating with study participants, caregivers, third-party vendors, and laboratories as needed.
• Assisting Coordinators with scheduling, copying, faxing, and other clerical tasks.
• Aiding Coordinators in the facilitation of study monitoring visits.
• Completion of daily responsibilities delegated by CRC as they pertain to the study and/or participants.
Responsibilities
- •Creating and maintaining patient charts for all assigned studies
- •Preparing participant visits based on CRC's schedule, ensuring all source documents, assessments, lab kits, and other visit materials are available and accurate
- •Filing of lab results, EKG results, and other communication in designated patient charts
- •Maintaining inventory of study-specific supplies, including lab kits, assessments, and participant-facing materials
- •Timely completion of data entry and query resolution for all CRFs, based on sponsor-specific timelines and deadlines established in contract or other communication
- •Assisting Coordinators in assessments, including but not limited to blood pressure, urine collection
- •Communicating with study participants, caregivers, third-party vendors, and laboratories as needed
- •Assisting Coordinators with scheduling, copying, faxing, and other clerical tasks
- •Aiding Coordinators in the facilitation of study monitoring visits
- •Completion of daily responsibilities delegated by CRC as they pertain to the study and/or participants
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