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Senior Wetland DelineatorSouthern CAWe are the Environment & Planning Division. You will join an existing team of Natural Resources professionals that includes wildlife biologists, botanists, aquatic resource biologists (waters, wetlands, and riparian areas), restoration ecologists, and regulatory specialists and will work closely with ICF project managers.
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ICF is seeking a Cyber Operations Specialist for a program responsible for ensuring critical infrastructure protection and resilience through effective collaboration between federal, private sector, and academic entities.
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50,000 for Waiver Programs, $57,500 for ICF Programs. Manage the day-to-day operations of one to four programs in a community including organization and implementation of direct supports, person-centered planning, and implementation, health care, advocacy, stakeholder relations, regulatory compliance, recruiting, retention, staffing, training, safety, financial management, and maintenance of the physical environment.
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Residential Habilitation (Res Hab) or Intermediate Care Facilities (ICF) experience is preferred. Manage the implementation of program planning; monitor the delivery of services and supports; ensure services are consistent, engaging, and relevant to the individuals served.
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Knowledge and understanding of clinical drug development strategic planning of clinical research, ICF, ICH GCP, GLP, In Vitro Diagnostic Regulation (IVDR) 2017/746, General Data Protection Regulation (GDPR) and clinical laboratory specimen handling.
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This position provides executive level leadership to Medicaid Waiver and Supervised Group Living (ICF/IDD) programs across Monroe, Lawrence and Bartholomew Counties in Southern Indiana. Demonstrates knowledge of all aspects of service provision and regulatiory standards including CARF, Indiana Department of Health (ICF/IDD), BQIS (Medicaid Waiver), Medicaid and other applicable standards.
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Will provide and schedule special trainings to increase the quality of care at each of the several ICF, IRA and Family Care homes including but not limited to activities of daily living, food planning and preparation, house and room maintenance, budgeting, and money management.
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The Talent Development Manager will advise on the planning and execution of learning and development programs that support and align with business strategy. ICF accreditation at the PCC level required.
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The ICF Natural Resources practice is currently seeking a full time Principal Biologist and Project Manager with education and experience in biology, environmental impact analysis, regulatory compliance (ESA, Clean Water Act, State species and water statutes), planning, and project management to support our HCP, ESA, and CEQA/NEPA work.
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Study Planning and Execution: Provides input on major milestones of trial, clinical trial plan and contingency planning; Analyzes and updates management on potential risks to study deliverables; Provides input on ICF creation; Oversees recruitment and retention; establishes and implements contingency plans for shortfalls; Consults & recruits members for DSMB and/or adjudication committee setup.
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Work with AVP, HR and OD and global talent partners to develop and oversee the management of performance management system, talent/succession planning process, and career development system, incorporating key organizational goals.
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The Clinical Research Associate (CRA) supports global and regional clinical trial managers and trial leaders in the planning, designing, executing, monitoring, and reporting of clinical trials.
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ICF is hiring a Senior Bat Biologist to join our Environmental Planning, Natural Resources, and Habitat Conservation Planning Teams. 4+ years of experience with ESA Section 7 and 10, habitat conservation plans, NEPA analyses, conservation planning, biological assessment preparation, agency coordination, and/or scientifically sound assessment of project effects.
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Study Planning: Contributes to clinical trial planning including identification of potential risks to study deliverables; development of contingency plan; development of protocol profile, protocol, and ICF template; selection of ARO, CRO, and members for DSMB and/or adjudication committee; development of charters for study committees (e.g., Executive Committee.
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Provide operational and strategic input into study planning and study specific documents such as synopsis, protocol, ICF, CRFs, CRF Completion Guidelines, Study Execution Plans, Clinical Data Review Plan, Clinical Database edit specifications, Clinical Study Report (CSR) development, etc.
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