System Administrator Salary at Deckwise® BETA

As a Learning Management System Administrator at CONMED, you will play a pivotal role in maintaining and optimizing our Learning Management System (LMS) globally, with the ultimate goal of enhancing our ability to consistently deliver exceptional results for healthcare providers and the patients they serve. You will be responsible for ensuring compliance of our training system in the highly regulated medical device industry. You will identify and implement improvements to our LMS, compliance and training programs in partnership with key stakeholders from HR, Quality, Legal, Operations and IT. This position offers a unique opportunity to make training even more effective, engaging and impactful for our employees, leading to the development of essential skills and valuable competencies. By aligning training efforts with organizational priorities, you will contribute significantly to the overall success of CONMED. This is a hybrid position in Largo, FL. - Oversee the learning management s

Linux Admin Hybrid Ogden UT Mid Level Systems Administrator This is a mid-level position. Provides functional and IT administration, integration, documentation, and implementation assistance on customer on-site issues which require a thorough knowledge of the related technical subject matter for effective system continuity. Participates in all phases of systems administration and customer support. Applies principals and methods of the functional area to difficult problems in technical areas to arrive at automated solutions. Performs as a member of a team or as a Team Lead as required. Must have 5-8 years of work experience. The candidate shall have the following skills/experience: UNIX/Linux experience with command line literacy. RedHat experience preferred Solve real-time challenges with the help of other systems administrators and fellow engineers Collaborate in a team environment Strong interpersonal communication skills MS Windows Server 2019 or higher MS SQL Server 2019 or higher

Join the team that is revolutionizing health care - BayCare Health System Our network consists of 16 community-based hospitals, a long-term acute care facility, home health services, outpatient centers and thousands of physicians. With the support of more than 30,000 team members, we promote a forward-thinking philosophy that's built on a foundation of trust, dignity, respect, responsibility, and clinical excellence. Title: Research Administration Specialist Facility: BayCare Systems Office (Hybrid) Responsibilities & Required Skills: Responsible for managing the administration of a specified portfolio of clinical research contracts throughout the clinical trial lifecycle for the purpose of maintaining financial compliance with both sponsor and government requirements. Responsible for supporting the Clinical Research Manager(s) associated with their assigned portfolio of specialties in developing coverage analysis reports and study budgets during study start-up. Also works with Patient

Overview: BrainCheck, Inc. has an immediate opening for a Part-Time Research Coordinator to contribute their efforts towards data collection in an active research project. We are looking for a Research Coordinator in or around Southwest Florida. This project involves direct engagement with older members of these communities on a day-to-day basis to collect data as efficiently and objectively as possible. You'll serve as the face of BrainCheck displaying appropriate decorum and demeanor when engaging with older individuals and participating organizations. Key responsibilities & Duties: Travel onsite to participating study locations within and around the designated region Assist with the coordination of site visits, correspond with study participants, disseminate and collect study related activities and materials, maintain study documents and information confidentially and securely Administer health related questionnaires, surveys and assessments Responsible for the recording and mainten

Description: Job Title: Clinical Research Coordinator Date Prepared: 02/27/2017 Status: Exempt EEO: Professional Date Revised: 01/12/2023 Statement of Purpose: The Clinical Research Coordinator (CRC) supports, facilitates, and coordinates the daily clinical trial activities under the direction of the Principal Investigator (PI). The CRC coordinates to support and complete the administration of the compliance, financial, personnel and other related aspects of the clinical study. Ensures that the best interests of all participants and the researchers are protected. Essential Functions: Coordinates with the PI, and the Director of Clinical Research (DCR); collaborating agencies, administration, and departments to help ensure that the clinical research and related activities are performed in accordance with Federal regulations and sponsoring agency policies and procedures. Collaborates with the PI and DCR to develop materials and tools necessary to appropriately train study participants in

As a Learning Management System Administrator at CONMED, you will play a pivotal role in maintaining and optimizing our Learning Management System (LMS) globally, with the ultimate goal of enhancing our ability to consistently deliver exceptional results for healthcare providers and the patients they serve. You will be responsible for ensuring compliance of our training system in the highly regulated medical device industry. You will identify and implement improvements to our LMS, compliance and training programs in partnership with key stakeholders from HR, Quality, Legal, Operations and IT. This position offers a unique opportunity to make training even more effective, engaging and impactful for our employees, leading to the development of essential skills and valuable competencies. By aligning training efforts with organizational priorities, you will contribute significantly to the overall success of CONMED. Oversee the learning management system and training compliance Design and i

Join the team that is revolutionizing health care – BayCare Health System Our network consists of 16 community-based hospitals, a long-term acute care facility, home health services, outpatient centers and thousands of physicians. With the support of more than 30,000 team members, we promote a forward-thinking philosophy that’s built on a foundation of trust, dignity, respect, responsibility, and clinical excellence. Title: Research Administration Specialist Facility: BayCare Systems Office (Hybrid) Responsibilities & Required Skills: Responsible for managing the administration of a specified portfolio of clinical research contracts throughout the clinical trial lifecycle for the purpose of maintaining financial compliance with both sponsor and government requirements. Responsible for supporting the Clinical Research Manager(s) associated with their assigned portfolio of specialties in developing coverage analysis reports and study budgets during study start-up. Also works with Patient

About the job Systems Administrator Top Secret Clearance Jobs is dedicated to helping those with the most exclusive security clearance find their next career opportunity and get interviews within 48 hours. Job Description:Type of Requisition:Regular Clearance Level Must Currently Possess:Top Secret/SCI Clearance Level Must Be Able To Obtain:Top Secret/SCI Suitability:Public Trust/Other Required:None Job Family:Systems Administration Skills:Job Qualifications:Information Technology (IT) Systems, Infrastructure Management (IM), Microsoft Windows Server, System Administration, Troubleshooting Certifications:Security+, CE - Sec+ CE Experience:3 + years of related experience US Citizenship Required:Yes Job Description:GDIT has an immediate opening for a Systems Administrator supporting infrastructure management on the CITS contract for USCENTCOM. The position is based in Tampa, Florida. Position Overview: The Systems Administrator will be responsible for maintaining and supporting Windows s