NewResearch Executive Assistant InsightResearch Executive AssistantDetroit, MIexperience in clinical research/clinical Trials and a strong understanding of research workflows, regulatory timelines, sponsor interactions, and site operations. Insight Health Systems Clinical Research Research Executive Assistant Title: Research Executive Assistant – Clinical Research.
Clinical Research TechnicianClinical Research Assistant Underfill University of MichiganClinical Research TechnicianClinical Research Assistant UnderfillAnn Arbor, MIThe Clinical Research Technician will also gain key skills in human subjects research process from start to finish, gain experience in 1:1 participant contact and expand knowledge on the intersection of community engagement and innovative research to improve risk reduction and substance use prevention services, particularly in underserved rural areas. In this role, the Clinical Research Technician will: Perform in-person and remote participant facing research activities including (but not limited to): engaging potential participants, screening for eligibility, conducting informed consent procedures, coordinating and scheduling research visits, and completing data collection and entry via survey/qualitative interviews/panels, etc.
NewClinical Research TechnicianClinical Research Assistant - Term Limited University of MichiganClinical Research TechnicianClinical Research Assistant - Term LimitedAnn Arbor, MICRC-tech will work with other team members to: organize and reach out to lists of participants that may be contacted for recruitment, Screen, informed consent, and enrollment of participants according to protocol for research studies, track and follow participants in study after their initial enrollment, enter and manage data, conduct chart reviews as necessary, prepare and send participant mailings, support the distribution of participant incentives, provide customer support around participant usage of the studies? technologies. The successful candidate for this position will participate in many aspects of research analysis and collaborative activities, with research programs including longitudinal cohorts, cross-sectional studies, clinical trials, health services and translational research with funding from a variety of sponsors including, NIH, industry, and others.
Research Grant/Contract Manager III - Cancer Clinical Research - 40 Hours - Days - Detroit Henry Ford HospitalResearch Grant/Contract Manager III - Cancer Clinical Research - 40 Hours - Days - DetroitDetroit, MIUtilizing project management tools and techniques, this role monitors financial aspects of multiple research grants, potential subcontracts or consultant agreements, and staffing data. In addition, this role will provide training to support staff regarding grant financial and institutional procedures and may be responsible for coaching and mentoring junior team members.
Research Study Coordinator II - Cancer Clinical and Translational Research Office - 40 Hours - Days Henry Ford HospitalResearch Study Coordinator II - Cancer Clinical and Translational Research Office - 40 Hours - DaysDetroit, MIOur staff have highly specialized roles in clinical coordination, research nursing, data management, regulatory coordination, grant management, and research sample processing. GENERAL SUMMARY: Under minimal supervision the Research Study Coordinator II: Coordinates research projects within guides of regulatory compliance and/or Code of Federal Regulation.
Research Study Coordinator III - Cancer Clinical & Translational Research - 40 Hours - Days Henry Ford HospitalResearch Study Coordinator III - Cancer Clinical & Translational Research - 40 Hours - DaysDetroit, MIOur staff have highly specialized roles in clinical coordination, research nursing, data management, regulatory coordination, grant management, and research sample processing. GENERAL SUMMARY: Under minimal supervision, the Research Study Coordinator III is responsible for coordinating research projects within guides of regulatory compliance and/or Code of Federal Regulation.
Research Study Coordinator III - Cancer Clinical & Translational Research - 40 hours - Days Henry Ford HospitalResearch Study Coordinator III - Cancer Clinical & Translational Research - 40 hours - DaysDetroit, MIOur staff have highly specialized roles in clinical coordination, research nursing, data management, regulatory coordination, grant management, and research sample processing. GENERAL SUMMARY: Under minimal supervision, the Research Study Coordinator III is responsible for coordinating research projects within guides of regulatory compliance and/or Code of Federal Regulation.
Research Study Coordinator III - Cancer Clinical & Trans Research - Full Time Henry Ford HospitalResearch Study Coordinator III - Cancer Clinical & Trans Research - Full TimeDetroit, MIDuties include but not limited to, interacting with both internal and external customers at all levels and oversight of recruitment and coordinating day-to-day operations of the study. GENERAL SUMMARY: Under minimal supervision, coordinates research projects within guides of regulatory compliance and/or Code of Federal Regulation.
Research Assistant/Associate (Survey Research Operations Manager) Wayne State UniversityResearch Assistant/Associate (Survey Research Operations Manager)Detroit, MI$65,000–$85,000 / yearEssential functions (job duties): Center for Urban Studies, a research center located within Wayne State University in Detroit, Michigan, seeks an experienced Survey Research Operations Manager to oversee the logistics and processes for implementing large-scale multi-mode surveys. Qualifications: A degree in social science research (including political science, public administration, demography, education, geography, psychology, public health, social work, sociology, survey methodology, statistics, and urban studies), especially coursework in research methods, is required.
Research Investigator-Research Assistant Professor University of MichiganResearch Investigator-Research Assistant ProfessorAnn Arbor, MIThe Prevention Research Collaborative brings together research teams from the CDC-funded Prevention Research Center, Michigan Youth Violence Prevention Center, Partners Engaged in Equity Research Hub, Healthy Minds Network, Housing Solutions for Health Equity, and several affiliated federally-funded research initiatives focusing on school and community-based approaches to promoting safe, healthy, and equitable communities. The Prevention Research Collaborative at the University of Michigan, School of Public Health is seeking a highly motivated researcher to support and expand the work of the Collaborative in the areas of youth development, mental health, violence prevention, and structural approaches to promoting health equity within school and community environments.
Research Study Coordinator II - Clinical & Trans Research - 40 Hours - Days Henry Ford HospitalResearch Study Coordinator II - Clinical & Trans Research - 40 Hours - DaysDetroit, MIGENERAL SUMMARY: Under minimal supervision, the Research Study Coordinator II, is responsible for: Coordinates research projects within guides of regulatory compliance and/or Code of Federal Regulation. Duties include but not limited to: Interacting with both internal and external customers at all levels and oversight of recruitment and coordinating day-to-day operations of the study.
Research Study Coordinator I - Cancer Clinical & Trans Research - 40 hours - Days Henry Ford HospitalResearch Study Coordinator I - Cancer Clinical & Trans Research - 40 hours - DaysDetroit, MIDuties include but not limited to, interacting with both internal and external customers at all levels and oversight of recruitment and coordinating day-to-day operations of the study. Reliable transportation to drive to various locations, Clinical skills including phlebotomy could be extremely useful but not required.
Clinical Research Assistant Opportunities - Multiple Locations Nationwide Headlands Research IncClinical Research Assistant Opportunities - Multiple Locations NationwideDetroit, MIThis general interest posting is designed for Clinical Research Assistants (RAs) who may not see a current opening that aligns with their location, but want to be considered for future opportunities across our growing network of clinical research sites nationwide. We welcome interest from candidates who bring: A bachelor's or master's degree involving 1+ year of laboratory classes, preferably within a scientific or healthcare-related field (e.g., biology, chemistry, psychology, pre-med, or similar) and/or.
Clinical Research Coordinator Associate underfill Technician or Assistant University of MichiganClinical Research Coordinator Associate underfill Technician or AssistantAnn Arbor, MICertification is required through Association of Clinical Research Professionals (ACRP) as a Certified Clinical Research Coordinator (CCRC) or Society of Clinical Research Association (SOCRA) as a Certified Clinical Research Professionals (CCRP) or equivalent. Candidates should be able (or willing to develop the ability) to perform most tasks independently, conduct quality checks of their own work, identify and use appropriate resources and support, and recognize when to escalate issues requiring additional intervention.
Clinical Research Coordinator Technician underfill Assistant University of MichiganClinical Research Coordinator Technician underfill AssistantAnn Arbor, MIPlease review SoCRAs Definition of a Clinical Research Professional for qualifying experience prior to applying.) or An advanced degree in a health-related areas such as: Health Sciences, Behavioral Sciences, Public Health, Health Care Administration, Clinical Research Administration, Social Work, Psychology, Epidemiology, Foreign MD. or Minimum 3 years of human subject experience (clinical, lab or health regulations) such as related patient care, related community health and wellness, related clinical information, and research. Michigan Medicine improves the health of patients, populations and communities through excellence in education, patient care, community service, research and technology development, and through leadership activities in Michigan, nationally and internationally.
Clinical Research Assistant Opportunities - Multiple Locations Nationwide Headlands ResearchClinical Research Assistant Opportunities - Multiple Locations NationwideDetroit, MIThis general interest posting is designed for Clinical Research Assistants (RAs) who may not see a current opening that aligns with their location, but want to be considered for future opportunities across our growing network of clinical research sites nationwide. We welcome interest from candidates who bring: A bachelor's or master's degree involving 1+ year of laboratory classes, preferably within a scientific or healthcare-related field (e.g., biology, chemistry, psychology, pre-med, or similar) and/or.
Clinical Research Coord Tech underfill Asst. University of MichiganClinical Research Coord Tech underfill Asst.Ann Arbor, MIPlease review SoCRAs Definition of a Clinical Research Professional for qualifying experience prior to applying.) or An advanced degree in a health-related areas such as: Health Sciences, Behavioral Sciences, Public Health, Health Care Administration, Clinical Research Administration, Social Work, Psychology, Epidemiology, Foreign MD. or Minimum 3 years of human subject experience (clinical, lab or health regulations) such as related patient care, related community health and wellness, related clinical information, and research. Michigan Medicine improves the health of patients, populations and communities through excellence in education, patient care, community service, research and technology development, and through leadership activities in Michigan, nationally and internationally.
Clinical Research Technician University of MichiganClinical Research TechnicianAnn Arbor, MIPlease review SoCRA's Definition of a Clinical Research Professional for qualifying experience prior to applying.) or An advanced degree in a health-related areas such as: Health Sciences, Behavioral Sciences, Public Health, Health Care Administration, Clinical Research Administration, Social Work, Psychology, Epidemiology, Foreign MD. or Minimum 3 years of human subject experience (clinical, lab or health regulations) such as related patient care, related community health and wellness, related clinical information, and research. Performs study procedures with minimal supervision; Schedules, assists with preparation for, and attends study initiation meetings, monitors, and audits; Ensures integrity of specimen management (collection, processing, packing/shipping, storing, labeling, tracking, etc.).
Research Assistant, Clinical/Population Sciences - Dept. Psychiatry and Behavioral Neurosciences Wayne State UniversityResearch Assistant, Clinical/Population Sciences - Dept. Psychiatry and Behavioral NeurosciencesDetroit, MIPreferred qualifications: Interpersonal Skills: Comfortable working in a fast-paced, team setting with diverse and/or clinical populations Schedule Flexibility: Must be available on-site for early morning, evening, or weekend visits or activities as needed Leadership: Demonstrated ability to work independently, manage a team, and multitask in a fast-paced research setting Technical Skills: Proficient in Microsoft Office; willingness to learn study software (e.g., REDCap, Ripple) Preferred Experience: Human subjects research and IRB processes Programming/statistical software (e.g., R, SPSS) REDCap or similar research software Scientific publications or presentations Health Compliance: Must be fully vaccinated and adhere to university health policies Commitment: Priority given to applicants interested in a minimum two-year commitment. Unique duties: The Trauma History Investigation of Neurodevelopment in Kids (THINK) Lab (wsuthinklab.com), directed by Dr. Hilary Marusak at Wayne State University, is seeking an experienced Research Assistant to assist with ongoing clinical research studies.
Research Data Assistant - Center for Social Work Research Wayne State UniversityResearch Data Assistant - Center for Social Work ResearchDetroit, MIThe position supports compliance with reporting requirements for the Substance Abuse and Mental Health Services Administration (SAMHSA) State Opioid Response (SOR) 4 grant administered through the Michigan Department of Health and Human Services (MDHHS), including timely entry of agency-level and client-level data, and preparation of required reports. The position is responsible for collecting, entering, organizing, cleaning, verifying, and reporting data to support research projects and federally and state-funded grant requirements.