+ Plus many more! Assists with the day-to-day administrative project management for multiple research studies with different Principal Investigators. + The longer you stay, the more vacation you'll accrue! * Assist with the administration of clinical research projects, recruiting investigators, collecting investigator documentation and site management Preferred: One (1) or more additional years of experience with Phase 1 studies (as a Clinical Research Coordinator or as a CRA). SimplyHired ranks Job Ads based on a combination of employer bids and relevance, such as your search terms and other activity on SimplyHired. At ICON, it's our people that set Principal Investigators (PIs) in the MCC conduct clinical trials to test new treatments for people affected by cancer. Clinical Administrator 3. This policy affects all employees, residents, fellows, students, contractors, new hires, visiting scholars program participants, adjunct faculty, and volunteers who work, train, or collaborate at the John S. Dunn Behavioral Science Center. Learn and prepare for new clinical research studies at the site (typically 1-2 new clinical studies per month). + 100% paid medical premiums for our full-time employees Read and interpret clinical trial study documents including protocol,, The Clinical Research Coordinator 1 serves as an entry level clinical research professional that has a basic foundation in clinical research through assigned, 7 to 9 years of clinical research experience and/or experience in CTI clinical project management demonstrating a clear and thorough understanding of global, 0-2 years of clinical or laboratory research experience. ** The Smidt Heart Institute reflects Cedars-Sinai's steadfast dedication to heart disease and research innovation giving patients access to the highest level of care. Our full-featured web hosting packages include everything you need to get started with your website, email, blog and online store. This position may include work involving potentially hazardous chemical, biological or radioactive agents. * Performs all other duties as assigned. The clinical research coordinator will be provided with a cubicle and a standard Partners computer in an office setting. Headquartered in San Diego, California, Dexcom has emerged as a leader of diabetes care technology. Build HUGE Income Selling Something People MUST Own. CC BY 4.0 This site requires JavaScript to work correctly. Use LoopiaWHOIS to view the domain holder's public information. For more information on our benefits programs please refer to the UTHealth Office of Benefits Website. https://www.uth.edu/benefits/benefits-summary.htm The Clinical Trials Regulatory Research Associate is responsible for the development and maintenance of regulatory documents pertaining to the clinical trials conducted by investigators at the Cancer Center. Displayed here are Job Ads that match your query. Gary Ford FlickrGlenn Ford was born Gwyllyn Samuel Newton Ford . Experience with study budget development and negotiation is preferred. Find job postings in CA, NY, NYC, NJ, TX, FL, MI, OH, IL, PA, GA, MA, WA, UT, CO, AZ, SF Bay Area, LA County, USA, UAE, SA, North America, abroad. craigslist: raleigh jobs, apartments, for sale, services, community. Job Summary The Clinical Research Associate position at Medpace offers the unique opportunity to have an exciting career in the research of drug and medical device development while making a differ Clinical Research Associate - Life Sciences Advanced Degrees (PhD/Post Doc). 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Successful * With the support of the Director, defines and communicates job descriptions, core competencies, performance standards. The clinical research associate will help drive the clinical trial process for several sample collections including submitting protocols, ordering supplies, performing site initiation visits with our physicians, and monitoring the quality of the samples and paperwork we receive. Clinical Research Program ManagerApply (https://usc.wd5.myworkdayjobs.com/ExternalUSCCareers/job/San-Diego-CA/Clinical-Research-Program-Manager.REQ20126284/apply) Keck School of Medicine San Diego, California + Must have a thorough knowledge of clinical research concepts, practices, and FDA regulations and ICH Guidelines regarding drug development phases, clinical research, and medical writing standards; demonstrated ability to interpret and apply these guidelines to document writing. Clinical Operations 3. See salaries, compare reviews, easily apply, and get hired. ! Minimum of a bachelors degree; Health or life science related field preferred; Willing to travel approximately 60-80% nationally; Strong communication and presentation skills a plus. Scheduling patients for clinical trial visits. Share why your MD is useful in trials (detecting symptoms for patients and understanding enrollment criteria). * Liaise with a broad spectrum of internal and external parties, including but not limited to clinical program leadership, investigators, clinical research coordinators and department research support staff, industry sponsors and auditors/monitors. Listed on 2023-01 Oct 27 Apprentice Plumbing Technician / Helper San. See our article on how to work remote in clinical research from home: 5 TIPS AND TRICKS TO WORKING FROM HOME IN CLINICAL RESEARCH DURING A PANDEMICOR REMOTELY. Forest Technologist Entry Level Program (FTELP) BC Public Service 3.2. + Work closely with Sales Automation to implement company-wide projects and procedures Study Site In this role, you will assist the Sales & Catering and Revenue Management teams with managing and maintaining the Delphi.fdc (FDC) database system on the property level, managing Definite bookings, End of Month reporting, lead catching, and user Salesforce training. In addition, all UTHealth employees who are assigned to work at a location that is subject to the affiliated partner's hospital, clinical offices, or agency are required to abide by UTHealth's rules and regulations, as well as the affiliate's rules and regulations, including COVID-19 vaccination and safety requirements. You need a good resume to find the job you want (Stockton). Clinical Research Associate 3. Read more at loopia.com/loopiadns . May review contracts and develop training. Provides work administrative direction and guidance to administrative staff personnel within department. Please, activate it in the options of your browser. **Once you join us you wont want to leave. The CRA position provides many other distinctive advantages including: Dynamic working environment, with varying responsibilities day-to day Defined CRA promotion and growth ladder with potential for mentoring and management advancements Competitive pay and opportunity for significant travel bonus Clinical Study Manager 1. The CMRPD provides comprehensive clinical trials management and oversight support to the various clinical research initiatives of the NCI/DCP. **The role: CLINICAL TRIAL MANAGER Internal Medicine** The Clinical Trial Manager is responsible for the delivery of all clinical aspects of the study. UTHealth includes The University of Texas Harris County Psychiatric Center, as well as the growing clinical practices UT Physicians, UT Dentists and UT Health Services. 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