RESEARCH ASSISTANT - Full Time
Behavioral Health Market Context
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Job Description
ical Research Department.
• Ensure that patients are appropriately scheduled for study related activities in compliance with the protocol, while assuring confidentiality of patient information.
• Recruitment of Study participants so must review and comprehend each assigned protocol including study proceedings and timelines, inclusion and exclusion criteria, confidentiality and privacy protections.
• Assists with sponsor prequalification visits, monitor visits, study termination visits.
• Responsible for compilation, registration and submission of data within regulatory timelines; maintains current and accurate protocol documentation, monitors and ensures study compliance with intense monitoring of study specific requirements, and maintains a system for effective data flow associated with research protocols.
• Assists with forms and data entry (EPIC, EDC, ect.). Assists with data clarification requests in a timely manner.
• Is familiar and in compliance with clinical research and related activities are performed in accordance with Federal regulations, BFS, sponsoring agency and RMC policies and procedures.
• Assists with required logs for patients and or studies and or Department. Assist with ordering and stocking of all materials for each clinical trial protocol and department needs.
• Works collaboratively with the other members of the clinical research team and the clinical and administrative support teams to ensure all protocols are followed and that there is timely documentation and submission of study data.
• Prep source charts, ensuring the most recent version of the source is always utilized.
• Assist with specimen processing, shipping and handling.
• Assists with establishing and organizing study files, including but not limited to, regulatory binders, study specific source documentation and other materials as required. Assists the Research Coordinator(s) and/or Principal Investigator(s) in submission of accurate and timely closeout documents to applicable Federal agencies, Riverside Medical Clinic for Sight, and the sponsoring agency in accordance with Federal regulations and institutional policies and procedures.
Requirements
• High school diploma or general education degree (GED) required.
• One to two years related experience and/or training; or equivalent combination of education and experience in clinical research, including recruitment, reporting, specimen processing and handling and source documentation.
• Good Clinical Practice (GCP); IATA and NIH current certificates or obtained within 4 weeks of hire.
Benefits
• Challenging and rewarding work environment
• Growth and Development Opportunities within UHS and its Subsidiaries
• Competitive Compensation
• Ensure that patients are appropriately scheduled for study related activities in compliance with the protocol, while assuring confidentiality of patient information.
• Recruitment of Study participants so must review and comprehend each assigned protocol including study proceedings and timelines, inclusion and exclusion criteria, confidentiality and privacy protections.
• Assists with sponsor prequalification visits, monitor visits, study termination visits.
• Responsible for compilation, registration and submission of data within regulatory timelines; maintains current and accurate protocol documentation, monitors and ensures study compliance with intense monitoring of study specific requirements, and maintains a system for effective data flow associated with research protocols.
• Assists with forms and data entry (EPIC, EDC, ect.). Assists with data clarification requests in a timely manner.
• Is familiar and in compliance with clinical research and related activities are performed in accordance with Federal regulations, BFS, sponsoring agency and RMC policies and procedures.
• Assists with required logs for patients and or studies and or Department. Assist with ordering and stocking of all materials for each clinical trial protocol and department needs.
• Works collaboratively with the other members of the clinical research team and the clinical and administrative support teams to ensure all protocols are followed and that there is timely documentation and submission of study data.
• Prep source charts, ensuring the most recent version of the source is always utilized.
• Assist with specimen processing, shipping and handling.
• Assists with establishing and organizing study files, including but not limited to, regulatory binders, study specific source documentation and other materials as required. Assists the Research Coordinator(s) and/or Principal Investigator(s) in submission of accurate and timely closeout documents to applicable Federal agencies, Riverside Medical Clinic for Sight, and the sponsoring agency in accordance with Federal regulations and institutional policies and procedures.
Requirements
• High school diploma or general education degree (GED) required.
• One to two years related experience and/or training; or equivalent combination of education and experience in clinical research, including recruitment, reporting, specimen processing and handling and source documentation.
• Good Clinical Practice (GCP); IATA and NIH current certificates or obtained within 4 weeks of hire.
Benefits
• Challenging and rewarding work environment
• Growth and Development Opportunities within UHS and its Subsidiaries
• Competitive Compensation
Qualifications
- •High school diploma or general education degree (GED) required
- •One to two years related experience and/or training; or equivalent combination of education and experience in clinical research, including recruitment, reporting, specimen processing and handling and source documentation
- •Good Clinical Practice (GCP); IATA and NIH current certificates or obtained within 4 weeks of hire
Benefits
- •Challenging and rewarding work environment
- •Growth and Development Opportunities within UHS and its Subsidiaries
- •Competitive Compensation
Responsibilities
- •SUMMARY: Assist Clinical Research and Coordination of Clinical Trials
- •Assists the Clinical Research Coordinator(s), Medical Director and Providers the research assistant will be responsible for supporting multiple research activites to assure efficacy and regulatory compliance of protocol, and data management projects as needed to meet the needs of the Clinical Research Department
- •Ensure that patients are appropriately scheduled for study related activities in compliance with the protocol, while assuring confidentiality of patient information
- •Recruitment of Study participants so must review and comprehend each assigned protocol including study proceedings and timelines, inclusion and exclusion criteria, confidentiality and privacy protections
- •Assists with sponsor prequalification visits, monitor visits, study termination visits
- •Responsible for compilation, registration and submission of data within regulatory timelines; maintains current and accurate protocol documentation, monitors and ensures study compliance with intense monitoring of study specific requirements, and maintains a system for effective data flow associated with research protocols
- •Assists with forms and data entry (EPIC, EDC, ect.). Assists with data clarification requests in a timely manner
- •Is familiar and in compliance with clinical research and related activities are performed in accordance with Federal regulations, BFS, sponsoring agency and RMC policies and procedures
- •Assists with required logs for patients and or studies and or Department
- •Assist with ordering and stocking of all materials for each clinical trial protocol and department needs
- •Works collaboratively with the other members of the clinical research team and the clinical and administrative support teams to ensure all protocols are followed and that there is timely documentation and submission of study data
- •Prep source charts, ensuring the most recent version of the source is always utilized
- •Assist with specimen processing, shipping and handling
- •Assists with establishing and organizing study files, including but not limited to, regulatory binders, study specific source documentation and other materials as required
- •Assists the Research Coordinator(s) and/or Principal Investigator(s) in submission of accurate and timely closeout documents to applicable Federal agencies, Riverside Medical Clinic for Sight, and the sponsoring agency in accordance with Federal regulations and institutional policies and procedures
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