Principal Investigator (Neurology) Professional Case ManagementPrincipal Investigator (Neurology)Garden City, MI$156,600–$266,700 / yearRisks to research subjects are minimized by using procedures which are consistent with sound research design and which do not unnecessarily expose the subjects to risk; and, whenever appropriate, by using procedures already being performed on the subjects for diagnostic or treatment purposes; Risks to human research subjects are reasonable in relation to the anticipated benefits (if any) to the individual, and the importance of the knowledge that may be expected to result; Selection of human subjects and patients for research participation is equitable; Individuals are adequately informed of the risks and benefits of research participation and the procedures that will be involved in the research, and that informed consent will be obtained from each prospective human research subject, or his/her legally authorized representative, in accordance with, and to the extent required, by company policies and federal regulations; Informed consent of human research subjects will be obtained in advance of research participation and appropriately documented in accordance with, and to the extent required, by company policies and federal regulations; Where appropriate, there is routine monitoring of the data collected to ensure the safety of human research subjects; The privacy of human research subjects is protected and the confidentiality of data is maintained; Appropriate additional safeguards are included in the study to protect the rights and welfare of human research subjects who are likely to be vulnerable to coercion or undue influence (e.g., children, prisoners, individuals with impaired decision-making capacity, or economically or educationally disadvantaged persons). Maintaining adequate, current, and accurate records of research data, outcomes, and reportable new information to permit an ongoing assessment of the risk/benefit ratio of study participation; Reporting promptly any internal or external adverse event that is considered to be unexpected, serious, and possibly or definitely related to the study; Reporting promptly any significant changes in the risk/benefit of study participation; Ensuring that, in the event a research subject experiences a significant adverse event, every reasonable effort is made to provide the subject with adequate care to correct or alleviate the consequences of the adverse event to the extent possible; Ensuring that human research subjects are kept fully informed of any new information that may affect their willingness to continue to participate in the research study; Ensuring that all listed investigators have the appropriate credentials to conduct the portion of the study in which they are involved and have completed the applicable company required training modules; Ensuring that conduct of the research study adheres to Good Clinical Practice guidelines.
NewClinical Dietitian AramarkClinical DietitianHolland, MIHolland Hospital has a 189-bed main campus and is the only hospital in West Michigan to receive a 5-star rating every year since 2016 when the Centers for Medicare and Medicaid Services (CMS) began its rating system. So, no matter what you're pursuing - a new challenge, a sense of belonging, or just a great place to work - our focus is helping you reach your full potential.
Clinical Research Coordinator II - Troy, MI Iterative HealthClinical Research Coordinator II - Troy, MITroy, MichiganWe built a leading performance-driven network of 100+ sites across the US, Europe, India, and Australia, conducting research directly in the communities where care is delivered across gastrointestinal, hepatology, obesity, and cardiology. By combining deep clinical trial expertise with cutting-edge AI, we connect sponsors' scientific ambitions with high-performing research teams that expedite and expand access to novel therapeutics for patients in need.
International Medical Graduate (IMG) - Clinical Research Revival Research Institute, LLCInternational Medical Graduate (IMG) - Clinical ResearchSouthfield, MIAdditional 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.
Clinical Research Coordinator II - Pediatric Clinical Research Unit Washington University in St LouisClinical Research Coordinator II - Pediatric Clinical Research UnitSt Louis, WashingtonRoutinely implements and manages all phases of study/protocol including recruitment, enrollment and eligibility as well as informed consent; ensures compliance with protocol guidelines and requirements of regulatory agencies; establishes record-keeping systems; makes assessments and determinations of participants’ progress in the study; analyzes, investigates, and reports adverse events; makes decisions as when to notify physicians of issues, when to stop participant inclusion, and/or to make and/or recommend adjustment of the protocol of particular participants; resolves IRB/protocol management issues and recommends corrective action as appropriate; serves as liaison with funding or sponsoring agency. Position within the Pediatrics Clinical Research Unit (PCRU) assists investigators as coordinator of complex clinical research studies; responsible for multiple research studies simultaneously, acting as a liaison with the school, sponsoring agency, community and the study participants; responsible for managing and recording all phases of study protocol as required by sponsoring agency to ensure compliance.
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.
Clinical Research Associate II ICON PlcClinical Research Associate IIDetroit, MIICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a CRA II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.
Remote Community Based Clinical Coordinator - Care Manager - Mackinac County, MI Upper Peninsula Health PlanRemote Community Based Clinical Coordinator - Care Manager - Mackinac County, MISt. Ignace, MIRemoteWorks as a member advocate and collaborates with support teams, medical care offices, medical equipment companies, home health agencies, hospital care teams, and other parties to ensure appropriate discharge plan, care plan, and coordination of acute care and long-term care services. Preferred: Bachelor of science in nursing, limited licensed bachelor of social work, limited licensed master of social work, fully licensed bachelor of social work, or fully licensed master of social work.
Clinical Research Coordinator II - Troy, MI Iterative Scopes Inc.Clinical Research Coordinator II - Troy, MITroy, MIThis role is responsible for managing complex studies with minimal oversight while partnering closely with patients, investigators, sponsors, CROs, and internal teams to drive high-quality study execution and enrollment success. Perform protocol-required clinical procedures including vital signs, ECGs, specimen collection, investigational product accountability, and phlebotomy, as permitted by applicable regulations, training, and organizational policy.
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.
NewSenior Clinical Research Coordinator Iterative Scopes Inc.Senior Clinical Research CoordinatorFlowood, MICRC) at Iterative Health you will serve as a key team member within the clinical research site, overseeing complex studies while supporting staff development, operational performance, and high-quality patient experiences. This role combines hands-on study coordination with mentorship, process improvement, and cross-functional collaboration to help drive successful study execution, enrollment performance, and regulatory compliance.
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 Nurse- Start Up BAMF Health ManagementClinical Research Nurse- Start UpGrand Rapids, MichiganDevelop protocol-specific source documentation, workflows, and readiness checklists in collaboration with operations staff, and participate in quality control efforts to ensure startup documentation accuracy and procedural compliance. BAMF Health will reasonably accommodate qualified individuals with a disability so that they can perform the essential functions of a job unless doing so causes a direct threat to these individuals or others in the workplace and the threat cannot be eliminated by reasonable accommodation or if the accommodation creates an undue hardship to BAMF Health.
NewClinical Research Nurse - Mercy STL - Full Time MercyClinical Research Nurse - Mercy STL - Full TimeSt LouisThe Clinical Research Nurse is responsible for the day-to-day operational tasks related to clinical trials and performs a variety of duties including, but not limited to, volunteer recruitment, drug/device/supply inventory maintenance, interaction with physicians, nurses, office staff, patients, and clinical monitors. As a Clinical Research Nurse, you'll combine your nursing expertise with cutting-edge research, working alongside physicians, healthcare professionals, and industry partners to bring tomorrow's treatments to patients today.
Clinical Research Associate - Full-Service Syneos Health IncClinical Research Associate - Full-ServiceMITogether we share insights, use the latest technologies and apply advanced business practices to speed our customers' delivery of important therapies to patients. Selecting us as an employer secures a career in which you're guaranteed to: Collaborate with passionate problem solvers Partner with the most diverse team of experts in the industry.
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.
Assistant Clinical Manager, Registered Nurse, Med Surg Oncology - Full Time Henry Ford HospitalAssistant Clinical Manager, Registered Nurse, Med Surg Oncology - Full TimeSouthfield, MIAdditionally, U.S. News & World Report recognized the hospital as a High Performer (Top 10%) in Adult Specialty rankings for Gastroenterology & GI Surgery and Orthopedics (2025-2026), based on reputation, patient outcomes, safety, and structural measures. The hospital features a 25-bed Acute Psychiatric Care Unit, providing comprehensive inpatient behavioral health services for adults ages 18 and older, and is the only hospital within the health system to receive a 4-Star CMS Quality Rating.
Research Associate, Clinical Population Sciences - Department of Internal Medicine Wayne State UniversityResearch Associate, Clinical Population Sciences - Department of Internal MedicineDetroit, MIEssential functions (job duties): Job Purpose: Under the direction of the Principal Investigator, provide scientific, technical, regulatory, and administrative assistance to support clinical and population science (human subjects) research studies. Assist in the coordination and implementation of behavioral and population-based research protocols, including participant recruitment, regulatory compliance, data collection and management, and dissemination of research findings.
Clinical Manager - Reentry- LMSW, LPC, LCSW Cherry HealthClinical Manager - Reentry- LMSW, LPC, LCSWDetroit, MichiganThe Manager, Clinical - Reentry is responsible for overseeing the entire clinical process within the reentry program, including case management, therapy, treatment plan development, ancillary services, employment services, case reviews, group counseling, aftercare planning, and client case monitoring. Clinical Supervision and Process Oversight: Oversee the development of ancillary services, treatment methods, and strategies to meet the specific therapeutic needs of the resident population (e.g., education, vocational training, career development, and aftercare planning).
Assistant Clinical Manager, Registered Nurse, Cardiac Stepdown Intermediate Care - Full Time Henry Ford HospitalAssistant Clinical Manager, Registered Nurse, Cardiac Stepdown Intermediate Care - Full TimeSouthfield, MIThe hospital features a 25-bed Acute Psychiatric Care Unit, providing comprehensive inpatient behavioral health services for adults ages 18 and older, and is the only hospital within the health system to receive a 4-Star CMS Quality Rating. Additionally, U.S. News & World Report recognized the hospital as a High Performer (Top 10%) in Adult Specialty rankings for Gastroenterology & GI Surgery and Orthopedics (2025-2026), based on reputation, patient outcomes, safety, and structural measures.