Core Job Responsibilities• Responsible for compliance with applicable Corporate and Divisional Policies and procedures.• Ensure ACPRU Technician work schedule provides adequate coverage for clinical study activities.• Review Draft Protocols and provide comment on aspects of study that impact general Study Technician duties, ACPRU workflow and operational aspects of the studies conducted at the ACPRU. Is able to offer suggestions for improvement.• Maintain professional communication and interaction throughout all aspects of work at the ACPRU and with outside client groups. Is able to effectively communicate with all levels of AbbVie management.• Accurately comply with study protocol and SOP requirements and complete source data in PIMS or on source data worksheets. Is able to independently generate necessary source worksheets from study protocols. Ensure study documents are completed appropriately.• Ensure safety and confidentiality of all study subjects through diligent surveillance and training of study personnel on safety and operational aspects of compound under study. Ensure staff knows how to recognize safety and operational related events appropriately handle them and pass information along to next work shift. Ensure Study Coordinator is informed of safety updates in a timely manner.• Understand GCP requirements and potential risk of compliance deficiencies. Review policies and procedures and suggest improvements.• Initiate, manage and/or participate in quality and compliance improvement projects to assure ACPRU maintains compliance with all relevant AbbVie and regulatory standards.• Prepare and present multiple project progress reports to update management and keep project teams informed.• Create training programs regarding ACPRU operation, safety and clinical research topics for the ACPRU staff.• Mentor, coach and train Research Technician staff.

• Interact with Principal Investigator, Nursing, and Ancillary staff to organize study specific laboratory, technical, and facility needs • Assist with Research Technician staffing, training, and internal continued educational training• Serve as both a Research Technician Mentor & Trainer • Address training deficits and provide corrective action training for Nurses and Research Technicians• Serve as the point of contact in the absence of Management• Serve as a member of the SOP / Work Instruction Development Team• Serve as a member of study set-up team responsible for initiating set-up of Electronic Data Collection (EDC) Program: Phase 1 Management System (PIMS) to meet each study’s protocol requirements• Assist Data Management Team with monitoring the completion of all Source Documents, Case Report Forms (CRFs), Data Correction Forms (DCF), Data Queries, and Adverse Event Documentation • Serve as a member of the ABBIOS & Non-ABBIOS Electrocardiogram Reconciliation Team• Attend draft clinical study protocol meetings to identify potential issues that may impact the clinical research unit. Also offer suggestions and/or solutions to logistic concerns• Strong knowledge of FDA and ICH/GCP Guidelines• Excellent observational skills, analytical and conceptual capabilities• Effectively work and communicate with multiple cross-functional teams• Ability to work independently with minimal supervision

• First Sergeant supervising 300+ soldiers• Solder Management / Readiness• Plan, coordinate, and manage Annual Training• Plan, coordinate, and manage monthly mission essential tasks• Performance Review for the Enlisted Soldiers• Manage Unit Prevention Drug Testing Program for 300+ soldiers• Coordinate Administrative Department with Line of Duty Investigations, Coordinate Promotions and Awards for enlisted soldiers

• Interact with Principal Investigator, Nursing, and Ancillary staff to organize study specific laboratory, technical, and facility needs • Assist with Research Technician staffing, training, and internal continued educational training• Serve as both a Research Technician Mentor & Trainer • Address training deficits and provide corrective action training for Nurses and Research Technicians• Serve as the point of contact in the absence of Management• Serve as a member of the SOP / Work Instruction Development Team• Serve as a member of study set-up team responsible for initiating set-up of Electronic Data Collection (EDC) Program: Phase 1 Management System (PIMS) to meet each study’s protocol requirements• Assist Data Management Team with monitoring the completion of all Source Documents, Case Report Forms (CRFs), Data Correction Forms (DCF), Data Queries, and Adverse Event Documentation • Serve as a member of the ABBIOS & Non-ABBIOS Electrocardiogram Reconciliation Team• Attend draft clinical study protocol meetings to identify potential issues that may impact the clinical research unit. Also offer suggestions and/or solutions to logistic concerns• Strong knowledge of FDA and ICH/GCP Guidelines• Excellent observational skills, analytical and conceptual capabilities• Effectively work and communicate with multiple cross-functional teams• Ability to work independently with minimal supervision