Health System Specialist
Tucson, AZ · On-site
Develops and maintains a pre-review program that will coincide with the IRB, IACUC, SRS, IBC, CIRB, and/or R&D Committee review of all research involving human subjects, animal subjects, basic ...
Tucson, AZ · On-site
Develops and maintains a pre-review program that will coincide with the IRB, IACUC, SRS, IBC, CIRB, and/or R&D Committee review of all research involving human subjects, animal subjects, basic ...
Tucson, AZ · On-site
Develops and maintains a pre-review program that will coincide with the IRB, IACUC, SRS, IBC, CIRB, and/or R&D Committee review of all research involving human subjects, animal subjects, basic ...
Tucson, AZ · On-site
Responsible for maintaining the federal-wide assurance with the Office of Human Research Protection and ensuring IRBs are appropriately constituted and registered. * Responsible for maintaining the ...
Tucson, AZ · On-site
Responsible for maintaining the federal-wide assurance with the Office of Human Research Protection and ensuring IRBs are appropriately constituted and registered. * Responsible for maintaining the ...
Tucson, AZ · On-site +1
$76K - $98K/yr
Responsible for maintaining the federal-wide assurance with the Office of Human Research Protection and ensuring IRBs are appropriately constituted and registered. * Responsible for maintaining the ...
Tucson, AZ · On-site +1
$76K - $98K/yr
Responsible for maintaining the federal-wide assurance with the Office of Human Research Protection and ensuring IRBs are appropriately constituted and registered. * Responsible for maintaining the ...
Mesa, AZ · On-site
$13.50 - $17/hr
Participate in required research training (e.g., human subjects protection, Project SOPs). * Assist with general Biobank organization and administrative tasks as needed. Requirements Education ...
Mesa, AZ · On-site
$13.50 - $17/hr
Participate in required research training (e.g., human subjects protection, Project SOPs). * Assist with general Biobank organization and administrative tasks as needed. Requirements Education ...
Mesa, AZ · On-site
$13.50 - $17/hr
Participate in required research training (e.g., human subjects protection, Project SOPs). * Assist with general Biobank organization and administrative tasks as needed. Requirements Education ...
Mesa, AZ · On-site
$13.50 - $17/hr
Participate in required research training (e.g., human subjects protection, Project SOPs). * Assist with general Biobank organization and administrative tasks as needed. Requirements Education ...
Mesa, AZ · On-site
$13.50 - $17/hr
Participate in required research training (e.g., human subjects protection, Project SOPs). * Assist with general Biobank organization and administrative tasks as needed. Requirements: Education ...
Quick apply
Mesa, AZ · On-site
$13.50 - $17/hr
Participate in required research training (e.g., human subjects protection, Project SOPs). * Assist with general Biobank organization and administrative tasks as needed. Requirements: Education ...
Winslow, AZ · On-site
$56K - $62K/yr
Oversee the review, correspondence & approval of human research protocols with all regulatory authorities, including study closeout. Determine which research protocols or issues have additional ...
Winslow, AZ · On-site
$56K - $62K/yr
Oversee the review, correspondence & approval of human research protocols with all regulatory authorities, including study closeout. Determine which research protocols or issues have additional ...
Sun City, AZ · On-site
$66K - $83K/yr
Protects the rights and welfare of all human research participants involved in research in accordance with Federal regulations * Cooperates with GI Alliance RESEARCH compliance and monitoring efforts ...
Sun City, AZ · On-site
$66K - $83K/yr
Protects the rights and welfare of all human research participants involved in research in accordance with Federal regulations * Cooperates with GI Alliance RESEARCH compliance and monitoring efforts ...
Tucson, AZ · On-site
$95 - $130/hr
Protect the rights and welfare of all human research participants involved in research. * Cooperate with Iterative Health research compliance and monitoring efforts regarding the access, use, and ...
Tucson, AZ · On-site
$95 - $130/hr
Protect the rights and welfare of all human research participants involved in research. * Cooperate with Iterative Health research compliance and monitoring efforts regarding the access, use, and ...
Tucson, AZ · On-site
$23 - $30.50/hr
Support the protection of human research participants in compliance with federal regulations, GCP, HIPAA, and institutional policies * Maintain compliance with all site SOPs, privacy standards, and ...
Tucson, AZ · On-site
$23 - $30.50/hr
Support the protection of human research participants in compliance with federal regulations, GCP, HIPAA, and institutional policies * Maintain compliance with all site SOPs, privacy standards, and ...
Phoenix, AZ · On-site
Ensures assigned studies are conducted in accordance with the Food and Drug Administration (FDA), Office for Human Research Protections (OHRP), and Good Clinical Practices (GCP) guidelines, including ...
Phoenix, AZ · On-site
Ensures assigned studies are conducted in accordance with the Food and Drug Administration (FDA), Office for Human Research Protections (OHRP), and Good Clinical Practices (GCP) guidelines, including ...
Phoenix, AZ · On-site
$24 - $32/hr
Ensures assigned studies are conducted in accordance with the Food and Drug Administration (FDA), Office for Human Research Protections (OHRP), Good Clinical Practices (GCP), and institutional ...
Phoenix, AZ · On-site
$24 - $32/hr
Ensures assigned studies are conducted in accordance with the Food and Drug Administration (FDA), Office for Human Research Protections (OHRP), Good Clinical Practices (GCP), and institutional ...
Sun City, AZ · On-site
$66K - $83K/yr
Protects the rights and welfare of all human research participants involved in research in accordance with Federal regulations * Cooperates with GI Alliance RESEARCH compliance and monitoring efforts ...
Sun City, AZ · On-site
$66K - $83K/yr
Protects the rights and welfare of all human research participants involved in research in accordance with Federal regulations * Cooperates with GI Alliance RESEARCH compliance and monitoring efforts ...
Sun City, AZ · On-site
$66K - $83K/yr
Protects the rights and welfare of all human research participants involved in research in accordance with Federal regulations * Cooperates with GI Alliance RESEARCH compliance and monitoring efforts ...
Quick apply
Sun City, AZ · On-site
$66K - $83K/yr
Protects the rights and welfare of all human research participants involved in research in accordance with Federal regulations * Cooperates with GI Alliance RESEARCH compliance and monitoring efforts ...
Tucson, AZ · On-site
$65K - $81K/yr
... human research participants in accordance with federal regulations. * Maintain ongoing communication with the CRO, sponsor, research participants, Site Manager, and PI throughout the course of each ...
Tucson, AZ · On-site
$65K - $81K/yr
... human research participants in accordance with federal regulations. * Maintain ongoing communication with the CRO, sponsor, research participants, Site Manager, and PI throughout the course of each ...
Demonstrated knowledge and understanding of human research policies, regulations, procedures and standards as according to HIPAA, IRB, FDA, ICH, and GCP guidelines is required. Coordinates and ...
Demonstrated knowledge and understanding of human research policies, regulations, procedures and standards as according to HIPAA, IRB, FDA, ICH, and GCP guidelines is required. Coordinates and ...
Phoenix, AZ · On-site
Ensures assigned studies are conducted in accordance with the Food and Drug Administration (FDA), Office for Human Research Protections (OHRP), and Good Clinical Practices (GCP) guidelines, including ...
Phoenix, AZ · On-site
Ensures assigned studies are conducted in accordance with the Food and Drug Administration (FDA), Office for Human Research Protections (OHRP), and Good Clinical Practices (GCP) guidelines, including ...
$24.33 - $36.19/hr
Demonstrated knowledge and understanding of human research policies, regulations, procedures and standards as according to HIPAA, IRB, FDA, ICH, and GCP guidelines is required. Coordinates and ...
$24.33 - $36.19/hr
Demonstrated knowledge and understanding of human research policies, regulations, procedures and standards as according to HIPAA, IRB, FDA, ICH, and GCP guidelines is required. Coordinates and ...
Phoenix, AZ · On-site
$24.33 - $36.19/hr
Demonstrated knowledge and understanding of human research policies, regulations, procedures and standards as according to HIPAA, IRB, FDA, ICH, and GCP guidelines is required. Coordinates and ...
Phoenix, AZ · On-site
$24.33 - $36.19/hr
Demonstrated knowledge and understanding of human research policies, regulations, procedures and standards as according to HIPAA, IRB, FDA, ICH, and GCP guidelines is required. Coordinates and ...
Tucson, AZ · On-site
$53K - $66K/yr
Research Compliance Auditor Posting Number req26721 Department Human Subjects Protection Prgm Department Website Link Location Tucson Campus Address Tucson, AZ USA Position Highlights The Human ...
Tucson, AZ · On-site
$53K - $66K/yr
Research Compliance Auditor Posting Number req26721 Department Human Subjects Protection Prgm Department Website Link Location Tucson Campus Address Tucson, AZ USA Position Highlights The Human ...

8.1
Based on 671 frontline employees who took The Breakroom Quiz
50th of 290 rated public sector bodies
The Research Committee Manager position is vital within the ORD and the facilities where research programs are conducted. Research Program Managers provide the link between Veterans and highly innovative projects. Duties and responsibilities include but are not limited to:
Oversees and manages these programs and their activities, including preparation of committee and reviewer materials with appropriate documentation, ensuring projects are reviewed by appropriate personnel, and ensuring all outstanding issues related to project management are resolved in a timely manner.
Serves in an advisory capacity to the R&D Leadership, research investigators, research committee members, and research committee Chairs and others on issues relative to carrying out the institution's research activities involving the use of humans, animals, and safety procedures for investigative purposes.
Serves as the accreditation Facility Liaison.
Oversees the protocol review process of multiple programs and committees, ensuring projects are reviewed by appropriate personnel, including the Information System and Security Officer (ISSO) and Privacy Officer (PO), and issues related to project management are resolved.
Develops and maintains a pre-review program that will coincide with the IRB, IACUC, SRS, IBC, CIRB, and/or R&D Committee review of all research involving human subjects, animal subjects, basic laboratory science and the human research protection program.
Develops and manages required annual and semi-annual reviews of the assigned programs.
Stays informed on guidelines relating to security and safety in the conduct of research and advises Research and Safety leadership, as needed.
Educates the investigative community of local and external policies and procedures with regards to research involving animal and human subjects.
Develops reporting procedures, sampling techniques, and measurements at various points in the research committee process and research programs to identify problem areas or inherent weaknesses in work processes, procedures, information systems and content.
Responsible for maintaining the federal-wide assurance with the Office of Human Research Protection and ensuring IRBs are appropriately constituted and registered.
Responsible for maintaining the IBC registration with the National Institutes of Health Office of Science Policy and ensuring IBC is appropriately constituted and registered.
Responsible for maintaining the program's accreditation process for the Association for the Assessment and Accreditation for Laboratory Animal Care International (AAALAC).
Analyzes and evaluates each research project to ensure compliance with Federal and State regulations, including but not limited to VA, FDA, OHRP (Office of Human Research Protection), ORO, and other applicable regulatory and procedural requirements.
Develops programs, policies, and procedures within the Research.
Monitors quality assurance program implementation and indicators designed to prevent erroneous transactions and ineffective work practices and to verify adherence to quality assurance plans and requirements.
Responsible for alerting investigators of deficiencies found within their submissions and educating them as to the steps required to correct the deficiencies.
Assumes responsibility in preparing for all external reviews.
Research and/or analyzes problems, administrative issues, or program requirements as they relate to animal, human subject or safety research and the research review process.
Initiates or reviews correspondence for all research.
Oversees and refines customized, networked computerized databases to allow for timely tracking of research projects.
Serves as the electronic records system administrator for the Research Office.
Work Schedule: Full-time, Monday thru Friday, 8:00AM to 4:30 PM
Compressed/Flexible: Not authorized.
Telework: This position is not authorized for telework.
Virtual: This is not a virtual position.
Position Description/PD#: Health System Specialist/ PD99586S
Relocation/Recruitment Incentives: Not authorized.
Critical Skills Incentive (CSI): Not authorized.
Permanent Change of Station (PCS): Not authorized.
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Public administration and motion picture and video production
10,000+ Employees
Washington, DC, US