- Mayo Clinic (Jacksonville, FL)
- …to resolve problems and ensure efficient completion of research studies . Position Overview: Independently coordinates complex (ie interventional, therapeutic greater ... within the department. Performs administrative and regulatory duties related to the study as appropriate. Some travel may be required. Protocol Development and… more
- University of Maryland, Baltimore (Baltimore, MD)
- …in study design and provides expert recommendations regarding research studies . Supports and assists with development and submission of grant proposals, ... written deliverables such as protocols, amendments, regulatory submissions, and study -related documentation throughout initiation, execution, and closeout. Assists and… more
- ThermoFisher Scientific (Middleton, WI)
- …the study team subject matter expert on the filing process for assigned studies . * Liaise with the clinical study team to resolve outstanding issues ... (WPD). This role also provides broad technical assistance to study teams. What You'll Do: * Process (scans/images, indexes,...You'll Do: * Process (scans/images, indexes, files) incoming study documents (paper and/or electronic). * Act as… more
- Johns Hopkins University (Baltimore, MD)
- …& Responsibilities** + Contribute as a member of a collaborative team to study design formulation. + Participate in development, testing and evaluation of manuals, ... data. + Develop and oversee design and implementation of study procedures and tools for data collection, eg participant...the next steps. + Identify and suggest ideas for sub- studies . + Extract data, review literature, and assist with… more
- Vitalief (New Brunswick, NJ)
- …tasks including patient screening, ordering tests, collecting specimens and study documentation of patient reported responses, relative to various Phase ... Participates in site preparation for trials including protocol feasibility, preliminary study budget, startup meeting preparation, training staff, and preparation of… more
- Parexel (Dover, DE)
- …in Clinical Trials** + Serve as **Medical Monitor** for gastroenterology studies , ensuring scientific integrity and patient safety + Provide expert medical ... oversight throughout the clinical trial lifecycle-from protocol development through study completion + Review and approve critical study documents including… more
- Albany Medical Center (Albany, NY)
- …is accountable for assisting in the timely and accurate conduct of research studies . Activities include participating in the study start up and termination ... procedures, working with study participants in various study tasks including patient recruitment, screening as well as data collection and study completion… more
- Dartmouth Health (Lebanon, NH)
- …with the medical team * Ensure that patients are scheduled for all study assessments as required per research protocol * Prepare and administer all medications ... and Informatics * Utilize electronic systems, technologies, and software necessary for study operations * Accurately document study visit assessments for data… more
- University of Pennsylvania (Philadelphia, PA)
- …FTDC's industry funded clinical trials portfolio focused on interventional studies in young onset neurodegenerative diseases including frontotemporal degeneration ... visit activities including recruitment, enrollment, collection and processing of study data and biological samples, data entry and queries,...includes but is not limited to supportive oversight of study teams, study conduct and study… more
- AbbVie (North Chicago, IL)
- …at a global level, including all affiliate offices who participate in GPRD studies as well as US Clinical Field Operations (UCFO) and International Clinical Field ... as needed. Assess workload and headcount needs based on study timelines and complexity of study and...based on study timelines and complexity of study and site issues. Responsible for consistency of performance… more
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