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Clinical Research Coordinator - Department of Psychiatry Wayne State University is searching for an experiencedClinical Research Coordinator - Department of Psychiatryat its Detroit campus location. Wayne State is a premier, public, urban research university located in the heart of Detroit, Michigan where students from all backgrounds are offered a rich, high-quality education. Our deep-rooted commitment to excellence, collaboration, integrity, diversity and inclusion creates exceptional educational opportunities which prepare students for success in a global society. Essential functions (job duties): Recruit, screen, obtain informed consent, and enroll eligible participants according to protocol for clinical studies. Schedule and coordinate participants study visits....

Provide study coordinator/data management/regulatory specialist support to the Clinical Trials Office (CTO). Responsibilities: Assure all studyrequirements are documented and meet both internal and externalregulations in accordance with protocol guidelines. Maintain logs,including tracker submissions and update the CTO Oncore database in atimely manner according to CTO SOPs. Respond to queriesin a timely fashion. Schedule andparticipate in monitoring visits and participate in multidisciplinary teamprogram meetings as required. Assistmultidisciplinary team in research activities. Bachelor's degree required or equivalent combination of education and experience. Medical and/or science experience/education preferred. Proficient with the Microsoft suite including Excel and Power point. Demonstrated attention to detail. Equal....

Provide study coordinator/data management/regulatory specialist support to the Clinical Trials Office (CTO). Responsibilities: Assure all studyrequirements are documented and meet both internal and externalregulations in accordance with protocol guidelines. Maintain logs,including tracker submissions and update the CTO Oncore database in atimely manner according to CTO SOPs. Respond to queriesin a timely fashion. Schedule andparticipate in monitoring visits and participate in multidisciplinary teamprogram meetings as required. Assistmultidisciplinary team in research activities. Bachelor's degree required or equivalent combination of education and experience. Medical and/or science experience/education preferred. Proficient with the Microsoft suite including Excel and Power point. Demonstrated attention to detail. Equal....

Provide study coordinator/data management/regulatory specialist support to the Clinical Trials Office (CTO). Manage independent assignment, providing excellent customer support and guidance in the clinical trials arena. Responsibilities: Assure all studyrequirements are met and documented and meet both internal and externalregulations in accordance with protocol guidelines. Maintain logs,including tracker submissions and update the CTO Oncore database in atimely manner according to CTO SOPs. Design systems forcoordinating, compiling and submission of data; design workflow processesand participate in quality assurance measures; coordinate site visits. Manage all patientand/or protocol data as assigned and respond to queries in a timelyfashion. Schedule andparticipate in monitoring visits....

Provide study coordinator/data management/regulatory specialist support to the Clinical Trials Office (CTO). Manage independent assignment, providing excellent customer support and guidance in the clinical trials arena. Responsibilities: Assure all studyrequirements are met and documented and meet both internal and externalregulations in accordance with protocol guidelines. Maintain logs,including tracker submissions and update the CTO Oncore database in atimely manner according to CTO SOPs. Design systems forcoordinating, compiling and submission of data; design workflow processesand participate in quality assurance measures; coordinate site visits. Manage all patientand/or protocol data as assigned and respond to queries in a timelyfashion. Schedule andparticipate in monitoring visits....

Provide study coordinator/data management/regulatory specialist support to the Clinical Trials Office (CTO). Manage independent assignment, providing excellent customer support and guidance in the clinical trials arena. Responsibilities: Assure all studyrequirements are met and documented and meet both internal and externalregulations in accordance with protocol guidelines. Maintain logs,including tracker submissions and update the CTO Oncore database in atimely manner according to CTO SOPs. Design systems forcoordinating, compiling and submission of data; design workflow processesand participate in quality assurance measures; coordinate site visits. Manage all patientand/or protocol data as assigned and respond to queries in a timelyfashion. Schedule andparticipate in monitoring visits....

Position Summary: Provide experienced Clinical Research Coordinator (CRC) support to the Clinical Trials Office (CTO) and Multidisciplinary Team (MDT) team. Independently manage a variety of assignments (including complex, early phase and multifaceted studies) as well as provide training and mentoring to KCI research team members. Function as primary support to service specific CRC Supervisor, providing coverage, as needed. This position is integral to the overall efficient operation of the CTO and activities related to research. Facilitate excellent customer service and guidance in the clinical trials arena . Essential Functions and Responsibilities: Ensure all study requirements are documented and meet both....

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries. Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You'll also have access to: Career development with an international company where you can grow the career you dream of. Free....

Clinical SLP Specialist Days FT - 2305003609 Description : DMC Rehabilitation Institute of Michigan is one of the nation’s largest hospitals specializing in rehabilitation medicine and research. RIM is known for its clinical expertise in spinal cord injury, brain injury, stroke, amputee, orthopedics and catastrophic injury care. The Institute houses the Center for Spinal Cord Injury Recovery and the Southeastern Michigan Traumatic Brain Injury System (SEMTBIS), one of only 16 federally designated model systems of care for brain injury care and research. RIM also operates 31 outpatient sites throughout southeast Michigan specializing in sports medicine and orthopedics. Job Summary Under....

Clinical Social Worker Case Management FT Days - 2406002668 Description : DMC Sinai-Grace Hospital is DMC’s largest hospital, offering a comprehensive heart center, cancer care, gerontology, emergency medicine, obstetrics/gynecology and cosmetic services. Sinai-Grace’s joint replacement program features a revolutionary minimally invasive knee and hip replacement surgery that attracts patients from all over the country. Sinai-Grace operates more than 21 outpatient care sites and ambulatory surgery centers throughout Wayne and Oakland Counties and is one of 10 hospitals in the nation to be awarded a Robert Wood Johnson Foundation grant to help set the standards of cardiac care for hospitals and....

At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You'll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world. A Day in the Life IN THIS ROLE YOU WILL PROVIDE DIRECT CLINICAL SUPPORT TO THE MEDTRONIC ENDOSCOPY PORTFOLIO Careers That Change Lives: The Clinical Specialist (CS) will be responsible for the implementation and training of Medtronic's Endoscopy Solutions customers and potential customers on clinical indications and applications of the Bravo pH Monitoring System, the ManoScan Manometry and pH-Impedance systems, the SmartPill System, and....

GENERAL SUMMARY: Under minimal supervision, coordinates clinical research projects in compliance with the Code of Federal Regulations. Provide technical support to Principal Investigators. Analyze protocol specific requirements and implement quality assurance measures to ensure physician, patient and clinician compliance. Abstract medical information from various sources in the patient medical record. Report adverse events to medical monitor, FDA, and all other governing bodies. Coordinate all external audits and monitoring visits, and serve as liaison between institution and sponsor. Serve as departmental and system-wide resource. EDUCATION/EXPERIENCE REQUIRED : Bachelor's degree in Clinical Research, Biology, Chemistry, Nursing or other closely related field. Two....

GENERAL SUMMARY: Under minimal supervision, coordinates clinical research projects in compliance with the Code of Federal Regulations. Provide technical support to Principal Investigators. Analyze protocol specific requirements and implement quality assurance measures to ensure physician, patient and clinician compliance. Abstract medical information from various sources in the patient medical record. Report adverse events to medical monitor, FDA, and all other governing bodies. Coordinate all external audits and monitoring visits, and serve as liaison between institution and sponsor. Serve as departmental and system-wide resource. EDUCATION/EXPERIENCE REQUIRED : Bachelor's degree in Clinical Research, Biology, Chemistry, Nursing or other closely related field. Two....

GENERAL SUMMARY: Under minimal supervision, coordinates clinical research projects in compliance with the Code of Federal Regulations. Provide technical support to Principal Investigators. Analyze protocol specific requirements and implement quality assurance measures to ensure physician, patient and clinician compliance. Abstract medical information from various sources in the patient medical record. Report adverse events to medical monitor, FDA, and all other governing bodies. Coordinate all external audits and monitoring visits, and serve as liaison between institution and sponsor. Serve as departmental and system-wide resource. EDUCATION/EXPERIENCE REQUIRED : Bachelor's degree in Clinical Research, Biology, Chemistry, Nursing or other closely related field. Two....

Under minimal supervision, coordinates clinical research projects in compliance with the Code of Federal Regulations. Provide technical support to Principal Investigators. Analyze protocol specific requirements and implement quality assurance measures to ensure physician, patient and clinician compliance. Abstract medical information from various sources in the patient medical record. Report adverse events to medical monitor, FDA, and all other governing bodies. Coordinate all external audits and monitoring visits, and serve as liaison between institution and sponsor. Serve as departmental and system-wide resource. Position is located at One Ford Place and Henry Ford Main Campus. EDUCATION/EXPERIENCE REQUIRED: Bachelor's degree in Clinical Research....

Under minimal supervision, coordinates clinical research projects in compliance with the Code of Federal Regulations. Provide technical support to Principal Investigators. Analyze protocol specific requirements and implement quality assurance measures to ensure physician, patient and clinician compliance. Abstract medical information from various sources in the patient medical record. Report adverse events to medical monitor, FDA, and all other governing bodies. Coordinate all external audits and monitoring visits, and serve as liaison between institution and sponsor. Serve as departmental and system-wide resource. EDUCATION/EXPERIENCE REQUIRED : Bachelor's degree in Clinical Research, Biology, Chemistry, Nursing or other closely related field. Two (2) years....

Under minimal supervision, coordinates clinical research projects in compliance with the Code of Federal Regulations. Provide technical support to Principal Investigators. Analyze protocol specific requirements and implement quality assurance measures to ensure physician, patient and clinician compliance. Abstract medical information from various sources in the patient medical record. Report adverse events to medical monitor, FDA, and all other governing bodies. Coordinate all external audits and monitoring visits, and serve as liaison between institution and sponsor. Serve as departmental and system-wide resource. EDUCATION/EXPERIENCE REQUIRED: Bachelor's degree in Clinical Research, Biology, Chemistry, Nursing or other closely related field. Two (2) years of....

Specialty/Competency: Functional & Industry Technologies Industry/Sector: Technology Time Type: Full time Travel Requirements: Up to 60% A career within Data and Analytics services will provide you with the opportunity to help organisations uncover enterprise insights and drive business results using smarter data analytics. We focus on a collection of organisational technology capabilities, including business intelligence, data management, and data assurance that help our clients drive innovation, growth, and change within their organisations in order to keep up with the changing nature of customers and technology. We make impactful decisions by mixing mind and machine to leverage data, understand and navigate....

Specialty/Competency: Functional & Industry Technologies Industry/Sector: Technology Time Type: Full time Travel Requirements: Up to 60% A career within Data and Analytics services will provide you with the opportunity to help organisations uncover enterprise insights and drive business results using smarter data analytics. We focus on a collection of organisational technology capabilities, including business intelligence, data management, and data assurance that help our clients drive innovation, growth, and change within their organisations in order to keep up with the changing nature of customers and technology. We make impactful decisions by mixing mind and machine to leverage data, understand and navigate....

Accenture is a leading global professional services company that helps the world's leading businesses, governments and other organizations build their digital core, optimize their operations, accelerate revenue growth and enhance citizen services-creating tangible value at speed and scale. We are a talent- and innovation-led company with approximately 742,000 people serving clients in more than 120 countries. Technology is at the core of change today, and we are one of the world's leaders in helping drive that change, with strong ecosystem relationships. We combine our strength in technology and leadership in cloud, data and AI with unmatched industry experience, functional expertise....