The Division of Infectious Diseases is excited to recruit an experienced Sr. Research Program Coordinator to lead protocol implementation for projects to improve health outcomes for people in India with tuberculosis. TB PuRe is a pulmonary rehabilitation clinical trial for TB patients in India. BRASS TACS is an observational cohort study examining the impact of drug resis

Requisition # 639488 Location Johns Hopkins Imaging, Baltimore, MD 21201 Category Manager/Supervisor Schedule Day Shift The Johns Hopkins Health System Corporation is a not for profit organization dedicated to providing the highest quality of care in the treatment and prevention of human illness. JHHS is an academically based health system consisting of The Johns Hopkins

Research Duties Verify participant eligibility for studies by comparing patient history with protocol requirements. Recruit participants from the Johns Hopkins Memory and Alzheimer's Treatment Center and other JH entities and complete informed consent process. Coordinate participant research visits. Visit participant within the participant home, as needed. Complete neurop

Requisition # 637200 Location Johns Hopkins Hospital, Baltimore, MD 21201 Category Nursing Schedule Evening Shift Elevate your possibilities The Johns Hopkins Children's Center Neonatal ICU Lactation Consultant is an important member of the multi disciplinary team who is responsible for the coordination, planning, and monitoring of patients and families related to breastf

Department of Geriatric Psychiatry and Neuropsychiatry is seeking a Research Program Coordinator to assist with clinical research involving the Clinic Cohort of the Johns Hopkins Alzheimer's Disease Research Center (JHADRC), working with participants who are cognitively normal, individuals with mild cognitive impairments and persons with dementia. Specific Duties & Respon

Assist in the management, development, and configuration of HLT tools, including machine translation engines, text classification models, transliteration, and optical character recognition Identify and address issues with the integration of technology Facilitate the use of Computer Assisted Translation (CAT) tools such as SDL Trados, including creating translation memory

Conduct coordination tasks and activities for knowledge translation and quality improvement projects at the Armstrong Institute under the guidance of the Program Manager. Develop and edit educational materials and tools, including presentations, scripts, manuals, and assessments. Schedule project meetings and document meeting progress/action items. Participate in developm

Monitor compliance with data quality assurance and quality control goals of clinical studies and follow all written and unwritten study practices, procedures and protocols. Maintain detailed working knowledge of assigned protocols; design and compile materials which aid investigators and other research staff in complying with protocol requirements. Ensure accuracy and tim

Working as an Assistant Director, you are responsible for assisting the Director of Environmental Services in directing and overseeing the operational needs of the Housekeeping Department. You will coordinate the tasks of the Operations Managers. You will serve as a liaison between administration and hospital departments and provide the highest possible level of service.

Working as an Assistant Director, you are responsible for assisting the Director of Environmental Services in directing and overseeing the operational needs of the Housekeeping Department. You will coordinate the tasks of the Operations Managers. You will serve as a liaison between administration and hospital departments and provide the highest possible level of service.

The Division of Gastroenterology and Hepatology is seeking a Sr. Clinical Research Program Manager for the GI Clinical and Translational Research Unit (CTRU). This position will report to CTRU leadership and work in collaboration with multiple investigators in the division. The Sr. Clinical Research Program Manager will be responsible for ensuring regulatory compliance, m

Maintain a good working knowledge of all assigned protocols and reporting requirements. Adhere to all protocol requirements to ensure validity of clinical research data. Interact with clinicians and other gatekeepers to access the patient population. Recruit research participants. Verify patient eligibility for studies. Interview patients. Collect patient specimens (e.g.,

Coordinate and oversee the day to day clinical research operations and serve as the primary contact for research related administrative and regulatory tasks (e.g. IRB compliance). Screen patients in the inpatient and outpatient setting for eligibility in ongoing research studies. Approach eligible patients for consent into appropriate research studies. Coordinate research

Do you consider yourself a self starter with an inner curiosity that drives innovation? Are you passionate about the future and bringing people together to translate a vision into reality? If so, we're looking for someone like you to join our team at APL. We are seeking a self motivated and enthusiastic professional that is well versed in government travel regulations to

Be familiar with good clinical practice guidelines and knowledge of sponsor and FDA guidelines. Works with the principal investigator (PI), or surrogate for the PI such as a research assistant to maintain current subcontracts for other universities and participating centers. Prepare annual reports to the NIH and subcontractors for multiple grants and contracts. Works unde