Clinical Research Assistant, MOSAAIC Study for Asian Americans
$19.23 - $24.04 per hourThe University Of Chicago
Department BSD IPP - MOSAAIC About the Department The Institute for Population and Precision Health (IPPH), located in the Biological Sciences Division, integrates a wide spectrum of factors such as human health behaviors, environmental factors, social and economic factors, policies and genetic determinants of health, into studies focused on the treatment and prevention of disease, as well as the maintenance of wellness. Leveraging and integrating the University of Chicago’s considerable institutional strength in population science with research spanning diverse fields such as genetic medicine, cancer epidemiology, microbiome, and epigenomics, the Institute has the common goal of improving human health outcomes. Another major goal of the Institute is to develop a multidisciplinary training program to equip researchers with emerging tools and methods to conduct precision health research within a population health framework. Our faculty lead research projects in biostatistics, epidemiology, and health services research, and participate in interdisciplinary teams with faculty in other departments to address complex problems in health and healthcare, in our communities and around the globe. Job Summary The job provides technical research support activities related to collecting, documenting, and reporting on basic clinical studies. Supports the administrative and operational tasks for clinical research conducted across the University. This at-will position is wholly or partially funded by contractual grant funding, which is renewed under provisions set by the grantor of the contract. Employment will be contingent upon the continued receipt of these grant funds and satisfactory job performance. This at-will position is wholly or partially funded by contractual grant funding which is renewed under provisions set by the grantor of the contract. Employment will be contingent upon the continued receipt of these grant funds and satisfactory job performance. Responsibilities Collects and maintains biometric data and biospecimens. Introduces patients at the UCMC and in the communities in the Community Mobile Clinic Van to the research study, answers questions pertaining to participation and consent, and may assist in administering tests &/or questionnaires following protocols. Performs blood draws and processing of blood and urine samples. Will be responsible to package and ship biological samples to an outside lab. Completes all activities by strictly following Good Clinical Practices (GCP) & all relevant current local, state, & federal laws, regulations, guidance, policy & procedure developed by the UChicago Institutional Review Board (IRB), Food & Drug Administration (FDA) Code of Federal Regulations (CFR), & the International Conference on Harmonization (ICH). Maintains detailed records of results which may include collecting, extracting & entering data; &/or preparing basic charts & graphs. Responsible for other duties such as preparing charts for the participant visits, setting up and cleaning the exam rooms before and after the visits, entering data as needed, performing data and equipment quality control checks, etc. Assists with and performs various administrative and operational tasks as assigned under direct supervision. Acquires and applies knowledge of clinical studies to collect analyzable clinical research data and/or samples. Performs other related work as needed. Minimum Qualifications Education: Minimum requirements include vocational training, apprenticeships or the equivalent experience in related field (not typically required to have a four-year degree). Work Experience: Minimum requirements include knowledge and skills developed through Certifications: --- Preferred Qualifications Education: Bachelor's degree in Epidemiology, Public Health, Nursing, Biology or closely related field. Experience: 1-yearrelevant research experience including experience with outreach efforts, study recruitment, and collecting biometric data. Phlebotomy experience. Wet lab sample processing experience. Preferred Competencies Knowledge in relevant scientific field. Knowledge of research techniques or methods. Knowledge of regulatory policies and procedures. Analytical skills. Problem-solving skills. Attention to detail. Organizational skills. Verbal and written communication skills. Ability to work independently and as part of a team. Knowledge of Microsoft Office. Working Conditions On-campus, office and clinic locations. Community partner locations. Application Documents Resume (required) Cover Letter (preferred) Job Family Research Role Impact Individual Contributor Scheduled Weekly Hours 40 Drug Test Required Yes Health Screen Required Yes Motor Vehicle Record Inquiry Required No Pay Rate Type Hourly FLSA Status Non-Exempt Pay Range $19.23 - $24.04 The included pay rate or range represents the University’s good faith estimate of the possible compensation offer for this role at the time of posting. Benefits Eligible Yes The University of Chicago offers a wide range of benefits programs and resources for eligible employees, including health, retirement, and paid time off. Information about the benefit offerings can be found in the Benefits Guidebook. Posting Statement The University of Chicago is an equal opportunity employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender, gender identity, or expression, national or ethnic origin, shared ancestry, age, status as an individual with a disability, military or veteran status, genetic information, or other protected classes under the law. For additional information please see the University's Notice of Nondiscrimination. Job seekers in need of a reasonable accommodation to complete the application process should call View phone number on click.appcast.io or submit a request via Applicant Inquiry Form. All offers of employment are contingent upon a background check that includes a review of conviction history. A conviction does not automatically preclude University employment. Rather, the University considers conviction information on a case-by-case basis and assesses the nature of the offense, the circumstances surrounding it, the proximity in time of the conviction, and its relevance to the position. The University of Chicago's Annual Security & Fire Safety Report (Report) provides information about University offices and programs that provide safety support, crime and fire statistics, emergency response and communications plans, and other policies and information. The Report can be accessed online at: Paper copies of the Report are available, upon request, from the University of Chicago Police Department, 850 E. 61st Street, Chicago, IL 60637. The University of Chicago is an urban research university that has driven new ways of thinking since 1890. Our commitment to free and open inquiry draws inspired scholars to our global campuses, where ideas are born that challenge and change the world. We empower individuals to challenge conventional thinking in pursuit of original ideas. Students in the College develop critical, analytic, and writing skills in our rigorous, interdisciplinary core curriculum. Through graduate programs, students test their ideas with UChicago scholars, and become the next generation of leaders in academia, industry, nonprofits, and government. To learn more about the university click here #J-18808-Ljbffr The University Of Chicago
$65k
Research Associate and Visiting Faculty in Women's Studies and Religion Please see Special Instructions for... ...(*). * Academic Rank Assistant Professor Associate Professor... ...Area of Study African American Religions African... ...Early Christianity East Asian Religions Ethics Hebrew...SuggestedFull time- AbbVie is seeking a Clinical Research Associate (CRA) to monitor clinical trial sites in the Madison area. You will collaborate closely with... ...compliance, data integrity, and subject safety across assigned studies. You will leverage risk-based monitoring approaches, utilize...Suggested
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...Japanese national to serve as a research associate and to deepen... ...management, and administrative assistance. Research areas include... ...DC, dedicated to promoting American leadership for a secure, free... ...in international relations, Asian studies, political science, security...SuggestedFull timeWork at office- ...Grants & Special Projects, the Clinical Research Associate coordinates all... ...CLINICAL TRIALS: Responsible for assisting in the selection and... ...research trials by reviewing studies, adhering to federal regulations... ...Certification issued by AHA-American Heart Association. The pay...SuggestedFull time
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- Brown University Health seeks a Clinical Research Assistant to assist in acquisition and analysis of patient information for multiple clinical research... .... You will interview patients, prepare and maintain study records, and enter data via computer while supporting statistical...
$115k - $140k
...your skills, knowledge, and clinical judgement to provide a high standard... ...based upon clinical research standards. Responsibilities Responsible... ...for all aspects of study site monitoring including routine... ...as assigned by management. Assist with training of new employees...Work at officeLocal areaRemote workNight shift$71.9k - $189k
...to ensure that sites are conducting the study(ies) and reporting study data as required... ...accordance with contracted scope of work and Good Clinical Practice.Work with sites to adapt, drive,... ...skill in applying, applicable clinical research regulatory requirements.Good therapeutic...Full timePart timeLocal areaImmediate startWorldwide- ...findings. Performs quality control studies and routine preventative... ...courteously and promptly. Assists in the orientation and training... ...experience in a healthcare, clinical setting, or a relevant area.... ...Certifications & Licensures American Society of Clinical Pathology...Full timePart timeWork experience placementReliefInternshipImmediate startFlexible hoursShift work
- The University of Miami is seeking a research support specialist to help implement prevention... ...data collection, coordination of study activities, and ensuring adherence to regulatory... ..., obtain informed consent, and assist with data entry and analysis under the guidance...
- ...A leading clinical research organization is seeking a Senior Study Manager to oversee all aspects of complex Phase I and II clinical trials. This role involves managing clinical pharmacology activities, ensuring adherence to budgets, and leading cross-functional teams...
$21 - $29.01 per hour
...business people, tech experts, researchers, and systems analysts to... ...statistical and analytical methods. -Assist in data interpretation and... ...'s Degree Related Field of Study required Can this role accept... ...of 1974, and Title I of the Americans with Disabilities Act of 1990...Hourly payDaily paidInternshipRemote workShift work$60k - $70k
...Senior Research Support Specialist ANNOUNCEMENT OF PROFESSIONAL... ...on trans-ancestry genetic studies exploring major depression, bipolar... ...analyze large-scale genomic, clinical, and behavioral datasets.... ...(PGC) and the Latin American Genomics Consortium (PGC). The...Full timeLocal areaMonday to Friday- University of Utah is seeking Clinical Study Coordinators to support clinical studies, ensuring protocol compliance and accurate documentation. The role includes participant recruitment, consent, logistics, and budget discussions, with emphasis on vaccinations per CDC...
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- PSI is a leading Contract Research Organization with more than 30 years... .... Job Description As a Clinical Research Associate at PSI you... ...monitoring tasks and work on clinical studies in different therapeutic... ...of Investigator newsletters Assist Site Management Associates in...Contract workWork visa
- ...expertise to the forefront of innovation. We are looking for a Clinical Research Associate (CRA) to join our A-team (remote; with travel). As... ...actively detect issues, provide solutions to ensure clinical studies are performed according to the trial protocol and in...Work at officeRemote workFlexible hours2 days per week
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