Research Computing Systems Assistant Manager University of Alaska AnchorageResearch Computing Systems Assistant ManagerFairbanks, AlaskaUAA : (Addresses Anchorage campus, Aviation Technology Complex, JBER - Elmendorf Extension, JBER - Richardson Extension, Kenai Peninsula College - Kachemak Bay campus, Kenai Peninsula College - Kenai River campus, Kodiak College, Kodiak High School Extension, Matanuska-Susitna College, Prince William Sound College, and Prince William Sound College - Cordova Extension) Online: https://www.uaa.alaska.edu/students/safety . * Each university within the University of Alaska system publishes an Annual Security and Fire Safety Report which contains information regarding campus safety and security including topics such as: campus law enforcement authority; crime reporting policies; campus alerts (Timely Warnings and Emergency Notifications); fire safety policies and procedures; programs to prevent dating violence, domestic violence, sexual assault and stalking; the procedures the University will follow when one of these crimes is reported; and other matters of importance related to security on campus.
GA Research: College of Business- Assistant East Texas A&M UniversityGA Research: College of Business- AssistantCommerce, TexasThis position offers graduate students the opportunity to gain hands-on experience in the research process while strengthening essential skills such as time management, academic writing, data analysis, critical thinking, and communication. The role contributes to advancing faculty research efforts while providing students with practical experience that supports academic and career growth.
Department of Radiology - Clinical Trials Research Associate University of IowaDepartment of Radiology - Clinical Trials Research AssociateIowa City, IAThe Clinical Trials Research Associate is responsible for the screening, recruitment, consenting, enrolling, assessment and monitoring of subjects for studies using novel magnetic resonance imaging to evaluate lung function in chronic lung diseases, including lung transplant rejection, asthma, chronic obstructive pulmonary disease, and lung cancer. The University of Iowa Health Care, Department of Radiology is seeking to hire one applicant for a Clinical Trials Research Assistant/Data Manager (25006305) or Research Associate (25006308).
Project Coordinator Research Brown University HealthProject Coordinator ResearchProvidence, RI$53,060.80–$87,547.20 / yearThe core Success Factors include: Instill Trust and Value Differences Patient and Community Focus and Collaborate RESPONSIBILITIES: Supervises non-MD/PhD research staff, assigns work tasks to research assistants and volunteers, coordinates work schedules, ensures completion of hospital and program required trainings, monitors staff adherence to procedures/protocols, and meets regularly with project team to ensure all study related tasks are being completed in a timely manner. Brown University Health employees are expected to successfully role model the organization''s values of Compassion, Accountability, Respect, and Excellence as these values guide our everyday actions with patients, customers and one another.
Research Laboratory Aide Arizona State UniversityResearch Laboratory AideTempe, AZJob Description: The research laboratory aide will assist PI Grodin in all aspects of her day-to-day laboratory tasks, including coordinating meetings, managing undergraduate students, submitting and managing IRB protocols, establishing laboratory data infrastructure, recruiting participants, and running participants through data protocols. Essential Duties: Essential duties include coordinating meetings, managing undergraduate students, submitting and managing IRB protocols, establishing laboratory data infrastructure, recruiting participants, and running participants through data protocols.
Clinical Research Coordinator Boston Children's HospitalClinical Research CoordinatorBoston, MACreates tracking systems and assist with developing processes to enhance efficiency and effectiveness of study operations and data management, such as patient appointment scheduling, and completion and tracking of study data and forms. Ensures on site and subcontract operations are consistent with overall study requirements for database maintenance, coding, completion and computer input of study forms, deadlines and other related issues.
NewClinical Research Coordinator II, Pediatrics (per diem) Boston Medical CenterClinical Research Coordinator II, Pediatrics (per diem)NY$42,500–$59,500 / yearJOB RESPONSIBILITIES: Recruits subjects to participate in the study by using approved methodologies; evaluates and tracks the eligibility of potential study participants; conducts the enrollment of study participants, including explaining research procedures, and obtaining informed consent; schedules study visits; conducts reminder phone calls, messages, or mailings. Administers study visits, qualitative interviews, quantitative assessments and surveys with participants and saves data according to study protocols, coordinates participant remuneration; organizes transcription of study visits and reviews and revises study visit transcripts for quality assurance.
Marine Research Specialist II University of Rhode IslandMarine Research Specialist IINarragansett, RI$55,000–$68,000 / yearIn furtherance of its mission to serve and support all learners as the state's public flagship university, URI continues to expand efforts to recruit and retain a broadly representative workforce as well as to regularly evaluate the effectiveness of those efforts. Contact Phone/Extension Contact Email Physical Demands Campus Location Narragansett Bay Campus Grant Funded Yes Extension Contingency Notes.
NewScientific Computing Research Expert MedcruitScientific Computing Research ExpertRemote$70–$80This could include data reduction, model fitting, simulation setup, instrument data processing, numerical solvers, inverse problems, or other computational research workflows. Build tasks around authentic scientific workflows such as data analysis, model fitting, simulation, numerical methods, or computational problem-solving.
Research Assistant Professor Charles R. Drew UniversityResearch Assistant ProfessorLos Angeles, CaliforniaWorks with investigators to formalize analysis plans and reporting specifications; advises as to choice of statistical analysis strategies, reliability of measurements and identifiability of models, and interpretation and presentation of statistical results. Builds and sustains collaborative relationships with individuals in different disciplines and serves as subject-matter expert for research teams, internal and external committees, and other constituencies and collaborators.
Assistant Clinical Research Coordinator UCSF Medical CenterAssistant Clinical Research CoordinatorSan Francisco, CAThe assistant CRC will be responsible for assisting with our outreach efforts in the Spanish-speaking community, scheduling in-person visits, scheduling blood draws, MRI scans, and neurological evaluations, carrying out cognitive assessments, scheduling ancillary studies like PET scans, Fitbit monitoring, and remote cognitive assessments. Abstracts clinical data from medical records; enters data onto case report forms, study flow sheets, and other forms; submits required data and data forms in accordance with accuracy and timeliness requirements of the protocols; addresses and resolves data queries; identifies, investigates and resolves data quality issues.
Assistant Director, RI NSF EPSCoR (Experimental Program to Stimulate Competitive Research) University of Rhode IslandAssistant Director, RI NSF EPSCoR (Experimental Program to Stimulate Competitive Research)Kingston, RI$90,000–$95,000 / yearAbout URI: The University of Rhode Island enrolls approximately 17,000 students across its graduate and undergraduate programs and is the State's flagship public research university, as well as the land grant and sea grant university, for the state of Rhode Island. POSITION SUMMARY: Provide strategic, operational, and administrative leadership for Rhode Island's NSF EPSCoR Cooperative Agreement "Rhode Island Network for Excellence in Science and Technology", which oversees the jurisdictional EPSCoR office.
Assistant Clinical Research Coordinator - Memory and Aging UCSF Medical CenterAssistant Clinical Research Coordinator - Memory and AgingSan Francisco, CAThe Assistant Clinical Research Coordinator may be responsible for the coordination of one or more single or multi-site, active or follow-up clinical studies and may help design flow sheets, data forms and source documents; gather and interpret medical, surgical and laboratory data regarding clinical subjects; may apply understanding of inclusion/exclusion eligibility criteria for protocols; help recruit, enroll, register, schedule and retain study subjects; record protocol specific treatments and assure collection and shipment of samples; assist research personnel to keep patients on study schedules; complete study forms to submit to sponsors and/or appropriate agencies; collect, enter and clean data into study databases, maintaining data quality; assist with data analysis; assist with preparation of reports and tables; attend team meetings; and perform other duties as assigned. Abstracts clinical data from medical records; enters data onto case report forms, study flow sheets, and other forms; submits required data and data forms in accordance with accuracy and timeliness requirements of the protocols; addresses and resolves data queries; identifies, investigates and resolves data quality issues.
Assistant Nurse Manager - Clinical and Translational Research Center University of Texas MD Anderson Cancer CenterAssistant Nurse Manager - Clinical and Translational Research CenterHouston, TX$111,000–$167,000 / yearInformation Requisition ID: 179622 Employment Status: Full-Time Employee Status: Regular Work Week: Days Minimum Salary: US Dollar (USD) 111,000 Midpoint Salary: US Dollar (USD) 139,000 Maximum Salary: US Dollar (USD) 167,000 FLSA: exempt and eligible for overtime, paid at a straight rate Fund Type: Hard Work Location: Onsite Pivotal Position: Yes Referral Bonus Available?: Preferred: Certification in Oncology, American Heart Association Basic Life Support (BLS), ACLS (Advanced Cardiac Life Support) or PALS (Pediatric Advanced Life Support) certification as required by patient care area.
Assistant Clinical Research Coordinator - Pediatric CHAMP Program UCSF Medical CenterAssistant Clinical Research Coordinator - Pediatric CHAMP ProgramSan Francisco, CADuties may include, but will not be limited to supporting the management and coordinating the tasks of single or multiple clinical research studies, depending on their size and complexity; act as intermediary between services and departments while overseeing data and specimen management; manage and report on study results; create, clean, update, and manage databases and comprehensive datasets and reports; manage Investigator's protocols in the Committee on Human Research online system, as well as renewals and modifications of protocol applications and the implementation of new studies; participate in the review and writing of protocols to ensure institutional review board approval within University compliance; help assure compliance with all relevant regulatory agencies; oversee study data integrity; implement and maintain periodic quality control procedures; interface with departments to obtain UCSF approval prior to study initiation; maintain all regulatory documents; report study progress to investigators; participate in any internal and external audits or reviews of study protocols; and perform other duties as assigned. The Assistant Clinical Research Coordinator will perform independently or with general direction at the fully operational journey level of the series to execute, manage, and coordinate research protocols, as directed by the Clinical Research Supervisor and/or Principal Investigator (PI); may coordinate the data collection and operations of two concurrent clinical research studies under the guidelines of research protocols, UCSF and regulating agency policies.
Assistant Research Scientist University of GeorgiaAssistant Research ScientistAthens, GAThe successful candidate should have strong analytical problem-solving skills, evidence of developing and validating analytical methods, and the ability to collaborate effectively with researchers from diverse disciplines while managing multiple client-driven projects, a demonstrated record of operating and maintaining chromatography and mass spectrometry instrumentation. This renewable 12-month position will lead the commissioning and operation of a new hybrid triple quadrupole/linear ion trap LC-MS/MS system and develop analytical services for a diverse client base spanning environmental science, ecology, agriculture, archaeology, forensics, biomedical research, and related fields.
Assistant Director of Research and Evaluation - WV Higher Education Policy Commission - Kanawha Co. State of West VirginiaAssistant Director of Research and Evaluation - WV Higher Education Policy Commission - Kanawha Co.Charleston, WVCollaborate with the West Virginia Higher Education Policy Commission, Council for Community and Technical College Education, West Virginia institutions of higher education, the West Virginia Department of Education, local county boards of education, the U.S. Department of Education, and external evaluators. Collaborate with the institutions of higher education, the WV Department of Education, U.S. Department of Education, local county boards of education and an external evaluator to collect, analyze, report, and utilize data to improve college access and success programming.
CALS_ Research Administrative Assistant- Grant Coordinator- Office of Pre-Award Services (Hybrid) Cornell UniversityCALS_ Research Administrative Assistant- Grant Coordinator- Office of Pre-Award Services (Hybrid)Ithaca, NY$26–$30.08 / hourWhile position responsibilities vary, every member of our community is expected to foster a culture of belonging and a psychologically healthy work environment by communicating across differences; being cooperative, collaborative, open, and welcoming; showing respect, compassion, and empathy; engaging and supporting others regardless of background or perspective; speaking up when others are being excluded or treated inappropriately; and supporting work/life integration of oneself and others. Under the direction of the Assistant Director/Team Lead and Grant and Contract Officers of the CALS Office of Pre-Award Services, in collaboration with eligible Principal Investigators (PIs), the Research Administration Assistant provides support for pre-award sponsored projects and other restricted proposal submissions as required.
Research Scientist/Engineer Assistant - Department of Global Health (Temporary) University of WashingtonResearch Scientist/Engineer Assistant - Department of Global Health (Temporary)Seattle, WashingtonThe sponsor requires that the successful candidate must be willing to train for 3-6 weeks on antimicrobial susceptibility testing; demonstrate proficiency by testing panels of blind isolates (2 times/year) and participate in 6 other proficiency testing events for molecular testing performed in the laboratory; and support ongoing rigorous quality assessment and continuous laboratory improvement activities. The individual will also contribute to ongoing research aimed at enhancing diagnostics for sexually transmitted infections, investigating commensal bacteria as potential reservoirs of antimicrobial resistance transferable to Neisseria gonorrhoeae, and investigating the host-pathogen interactions underlying gonococcal infections.
Research Regulatory Assistant Brown University HealthResearch Regulatory AssistantProvidence, RI$41,537.60–$68,556.80 / yearThe core Success Factors include: Instill Trust and Value Differences Patient and Community Focus and Collaborate RESPONSIBILITIES: The Regulatory Assistant supports clinical trials in an administrative manner and is responsible for the following duties:• white-space:pre Assist with the preparation and/ or collection of study related research required regulatory documents, including but not limited to:o white-space:pre CVso white-space:pre MLso white-space:pre Financial Disclosure Formso white-space:pre Conflict of Interest Formso white-space:pre FDA 1572o white-space:pre Delegation of Authority/ Staff Signature Logs• white-space:pre May collect signatures to ensure accuracy of study documents• white-space:pre Receives and processes clinical trial external safety reports, including SUSARs• white-space:pre May process and file IRB and RDC approvals; may update the Clinical Trial Management System• white-space:pre May complete minor revisions to clinical trials, such as personnel updates or continuing reviews• white-space:pre May assist with the preparation and and set-up of sponsor visits, such as Monitoring Visits, Site Initiation Visits and Close-Out Visits• white-space:pre Liaises with regulatory staff, sponsors, investigators, and research team members• white-space:pre Participates in Study Initiation Visits and Interim Monitoring Visits• white-space:pre Performs other duties as assigned MINIMUM QUALIFICATIONS: BASIC KNOWLEDGE:• white-space:pre Bachelor's degree in Applied or Life Sciences or related area, including courses in research methodologies and microcomputer systems. In lieu of a bachelor's degree, an additional 2-3 years of experience may be substituted.• white-space:pre Knowledge of theory and techniques of research methodology• white-space:pre Must possess the following skills:o white-space:pre Detail-oriented and excellent organizational skillso white-space:pre Strong-self-startero white-space:pre Interpersonal skillso white-space:pre Team-orientedo white-space:pre Excellent oral and written communication skillso white-space:pre Proficient in Microsoft office and in various database applicationsEXPERIENCE:6 months - 1 year in direct clinical trial administration experience or relevant administrative experience preferred but not required.