Travel Clinical Lab Scientist (CLS) - $1,520 to $1,747 per week in Commerce Township, MI AlliedTravelCareersTravel Clinical Lab Scientist (CLS) - $1,520 to $1,747 per week in Commerce Township, MICommerce Township, MI$1,520–$1,747Summary: The Clinical Laboratory Scientist (CLS) is responsible for conducting and overseeing a wide range of laboratory tests across multiple disciplines, including chemistry, hematology, microbiology, immunology, and blood banking. Job Details Fusion Medical Staffing is seeking a skilled Clinical Laboratory Scientist (CLS) – Generalist for a 13-week travel assignment in Commerce, Michigan.
NewClinical Research Coordinator Senior University of MichiganClinical Research Coordinator SeniorAnn Arbor, MIIn this role, the CRC Lead will coordinate and oversee regulatory activities, support harmonization of regulatory processes across participating sites, and work closely with the Principal Investigator, study leadership, and participating research teams to ensure compliance with applicable regulatory and study requirements. The CRC Lead will work closely with PCCM Project Managers and Principal Investigators, multidisciplinary clinical partners, internal and external study teams, and other stakeholders to ensure high-quality and efficient execution of the PCCM clinical research portfolio.
NewClinical Instructor-Clinical Professor University of MichiganClinical Instructor-Clinical ProfessorAnn Arbor, MIGlobally Respected Institution: Home to 150+ clinical and research faculty across 12 state-of-the-art locations where we provide comprehensive and subspecialized vision care and conduct groundbreaking research that changes lives. Collaborative Environment: Enjoy rich opportunities to work alongside top clinicians and researchers while partnering across U-M's leading schools in engineering, public health, business, and more.
Clinical Research Coord Senior University of MichiganClinical Research Coord SeniorAnn Arbor, MITechnical Skills: Proficiency in Microsoft Office Suite (Word, PowerPoint, Excel) and experience with research database and data management software such as REDCap (building a database, managing and troubleshooting); familiarity with file-sharing, reference management, communication platforms including Dropbox, google drive, Zotero, end note, etc. Research & Regulatory: Must have experience supporting study start-up, starting IRB applications from scratch and related submissions, study management, and closeout phases, including familiarity with general IRB processes, eResearch, and regulatory documentation.
Clinical Research Associate (CRA) - Oncology (Remote) Merck & Co IncClinical Research Associate (CRA) - Oncology (Remote)Livonia, MIRemote$96,200–$151,400 / yearConducts site visits including but not limited to validation visits, initiation visits, monitoring visits, close-out visits and records clear, comprehensive and accurate visit & non-visit contact reports appropriately in a timely manner. Works in partnership with GCTO country operations, finance, regulatory affairs, pharmacovigilance, legal and regional operations, HQ functional areas and externally with vendors and IRB/IECs and Regulatory Authorities in support of assigned sites.
Clinical Research Associate (Cra) - Oncology (Remote) Merck & Co., Inc.Clinical Research Associate (Cra) - Oncology (Remote)Livonia, MIRemote$96,200–$151,400 / yearConducts site visits including but not limited to validation visits, initiation visits, monitoring visits, close-out visits and records clear, comprehensive and accurate visit & non-visit contact reports appropriately in a timely manner. Works in partnership with GCTO country operations, finance, regulatory affairs, pharmacovigilance, legal and regional operations, HQ functional areas and externally with vendors and IRB/IECs and Regulatory Authorities in support of assigned sites.
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.
Clinical Instructor - Clinical Professor University of MichiganClinical Instructor - Clinical ProfessorAnn Arbor, MIFrom diagnosis and medical management of common cardiac disorders to groundbreaking therapies for complex congenital heart conditions, our team is committed to providing the most advanced evidence-based care for infants, children and adolescents with all forms of congenital and acquired heart disease, as well as for adults with congenital heart disease. The congenital catheterization laboratory offers congenital heart patients cutting-edge, minimally invasive care including the new Medtronic Harmony transcatheter pulmonary valve, hybrid procedures in collaboration with cardiac surgery, and participation in clinical trials such as the new ASD bioresorbable device trial (ASCENT).
Clinical Research Program Manager University of MichiganClinical Research Program ManagerAnn Arbor, MIThe Center?s mission is to optimize cardiometabolic health and reduce cardiovascular risk across the health system through a data science-driven, risk-based approach spanning six integrated cores: Population and Data Science, Phenotyping, Cardiometabolic Health Clinic and Clinical Trials, Health System Implementation, Industry and Academic Partnerships, and Training and Education. The Clinical Research Program Manager will serve as the operational backbone of this multidisciplinary clinical research enterprise, providing administrative and scientific coordination across active clinical trials, observational studies, and translational research initiatives.
NewClinical Research Technician University of MichiganClinical Research TechnicianAnn Arbor, MIWorks with investigator to: establish and implement procedures for ensuring data quality; review preliminary descriptive statistics from analyses to identify potential problems with data, and initiate corrective action; develop primary data collection/entry protocols, training and procedures manuals; monitor field procedures to determine compliance with protocol. Seeking a highly motivated, responsible, and detail-oriented Research Assistant to work collaboratively with project managers, program staff, therapists and investigators on a clinical trial examining effective treatments for PTSD.
Senior Clinical Research Associate - CNS/Rare Disease - Midwest (Remote) Worldwide Clinical Trials Holdings IncSenior Clinical Research Associate - CNS/Rare Disease - Midwest (Remote)MIRemote$97,000–$193,000 / yearTypically involved in all stages of the clinical study, including identifying potential sites to participate in the research effort, performing various study start-up activities such as working with sites to collect appropriate regulatory documents and supporting the negotiation of contracts and budgets, training the sites to collect data properly and report any potential safety-related events, managing the site's activities during study maintenance, and closing down research activities at the sites once the study has concluded. As a Clinical Research Associate (CRA) at Worldwide, you will find yourself working alongside brilliant minds across diverse therapeutic areas, including Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases.
NewClinical Research Coord Inter University of MichiganClinical Research Coord InterAnn 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. The CRC Intermediate will work within a small team to recruit participants, screen for eligibility, schedule appointments, collect informed consent, collect survey data, and administer tailor-made interventions one-on-one with parents over a period of 6 to 8 weeks per family.
Senior Clinical Data Manager (Remote - US) MMSSenior Clinical Data Manager (Remote - US)Canton, MIRemoteProvides oversight and resolves all issues in data management study processing activities including CRF tracking and data entry, integration of external electronic data (e.g., lab data) with clinical database, data validation and review, query processing and resolution, adverse event and medication coding, SAE reconciliation, database lock and database QC audits. Oversees and develops data management study documentation including Case Report Forms, CRF Completion Guidelines, Database Design via annotated CRFs, Validation specifications (edit checks), and Data Management Plan.
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 Coordinator Revival Research InstituteClinical Research CoordinatorDearborn Heights, MichiganMaster's Degree: A master's degree in a relevant field (such as clinical research, biostatistics, epidemiology, or healthcare management) may be preferred or allow candidates to enter the role with less practical experience, given the advanced knowledge and research skills acquired during their studies. Here's a detailed overview of the responsibilities and skills required for a CRC: Core Responsibilities: Regulatory Document Management: Manage essential regulatory documents, including Institutional Review Board (IRB) submissions and safety reports, ensuring compliance with all regulatory authorities and guidelines (e.g., FDA, DSMB).
Clinical Research Technician Underfill University of MichiganClinical Research Technician UnderfillAnn Arbor, MIMichigan 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. Staff members are expected to work independently when appropriate and regularly exercise good judgment in setting priorities, resolving operational problems, and applying policies, procedures, and methods, while maintaining the strictest of confidentiality at all times.
Addiction Research Area Specialist IntermediateAssociate Underfill - Clinical Intervention Specialist University of MichiganAddiction Research Area Specialist IntermediateAssociate Underfill - Clinical Intervention SpecialistAnn Arbor, MIAdditional qualifications that will help individuals succeed in this role at any level include: 3+ years of direct clinical experience providing counseling/ behavioral health support, or case management to individuals with substance use disorders or co-occurring mental health conditions delivering substance use-focused interventions using motivational interviewing, harm reduction, treatment readiness, trauma-informed care, overdose education and prevention, contingency management, or other evidence-informed approaches. Other day-to-day study-related tasks may include participant recruitment and retention, assisting with informed consent processes, tracking participant engagement, entering study data, participating in clinical supervision and fidelity monitoring, supporting quality assurance activities, and collaborating with community partners.
International Medical Graduate (IMG) - Clinical Research Coordinator Revival Research Institute, LLCInternational Medical Graduate (IMG) - Clinical Research CoordinatorSouthfield, MIFull timeAdditional Qualifications: Database and computer skills: Microsoft Office (Word, Excel), Outlook, excellent verbal and written communication skills, ability to work independently and assume responsibility, excellent organizational skills, ability to meet data deadlines and maintain confidentiality. Education/ Training: International Medical Graduate; MBBS, BMBS, MBChC, MBBCh, MD, DO, MCM, DM, MCM, MMSc, MMedSc, MM, MMed, MS, MSurg, MChir, MCh, ChM, CM, MSc, DCM, DClinSurg, DMSc, DMedSc, DS, DSurg.
RN Clinical Unit Leader - Emergency Department - Full Time - Variable - JACKSON Henry Ford HospitalRN Clinical Unit Leader - Emergency Department - Full Time - Variable - JACKSONJackson, MIThe Clinical Unit Leader (CUL) under general supervision from the department manager and/or director, and in accordance with policies and guidelines established within the organization and individual unit, priority is to function as shift supervisor and clinical liaison with staff, physicians, and management, providing continuity of leadership day to day. Ability to problem solve; effective verbal and written communication skills and interpersonal skills necessary for effective leadership of the patient care team.
RN Clinical Unit Leader - Maternal Child Administration - Full Time - Nights Henry Ford HospitalRN Clinical Unit Leader - Maternal Child Administration - Full Time - NightsJackson, MIGENERAL SUMMARY: The Clinical Unit Leader (CUL), under general supervision from the unit manager and/or director, and in accordance with policies and guidelines established within the organization and individual unit, priority is to function as shift supervisor and clinical liaison with staff, physicians, and management, providing continuity of leadership day to day. Ability to problem-solve, effective verbal and written communication skills, and interpersonal skills necessary for effective leadership of the patient care team.