NewPhysician Hematology/Oncology - Competitive Salary McLaren Medical GroupPhysician Hematology/Oncology - Competitive SalaryLansing, MIThe city speaks 63 different languages, boasts of New York level entertainment venues (Wharton Center and the Edythe and Eli Broad Art Museum), and offers either small town or urban city living options. McLaren includes 13 hospitals, ambulatory surgery centers, imaging centers, commercial and Medicaid HMOs, and a 590-member employed primary and specialty care physician network.
Clinical Research Coordinator- Neurology (Detroit, MI) Profound ResearchClinical Research Coordinator- Neurology (Detroit, MI)Detroit, MichiganOur Mission: Improving Lives by Providing Advanced Therapeutic Options Our Vision: Creating the Absolute Best Patient-Physician Experience in Clinical Research Our Values: Compassion: We prioritize the patient-physician relationship, ensuring every interaction is service-oriented and patient-centered. You’ll manage study activities from start-up through closeout, lead interactions with study participants, maintain audit-ready documentation, and work directly with investigators, sponsors, and CROs.
Clinical Research Coordinator (Detroit, MI) Profound Research LLCClinical Research Coordinator (Detroit, MI)Detroit, MILead, implement and coordinate duties for assigned clinical trials including but not limited to study start up, vendor management, subject recruitment, source document review and completion, protocol training, collection of regulatory documents, participant visits, timely data collection and documentation, management and reporting of adverse events, serious adverse events, and deviations, and monitoring visits and follow up. Ensure good documentation practices are applied by all team members when collecting, maintaining and correcting study data and required records of clinical trial activity including but not limited to source documentation, case report forms, queries, drug dispensation records, and regulatory forms.
Contractor- Assistant Clinical Research Coordinator (Detroit, MI) Profound ResearchContractor- Assistant Clinical Research Coordinator (Detroit, MI)Detroit, MichiganAs an Assistant Clinical Research Coordinator at Profound Research, you’ll work alongside experienced clinical research staff at one of our sites, supporting the day-to-day execution of high-volume vaccine clinical trials. Our Mission: Improving Lives by Providing Advanced Therapeutic Options Our Vision: Creating the Absolute Best Patient-Physician Experience in Clinical Research Our Values: Compassion: We prioritize the patient-physician relationship, ensuring every interaction is service-oriented and patient-centered.
Clinical Research Coordinator AssociateTechnician Assistant- Term limited University of MichiganClinical Research Coordinator AssociateTechnician Assistant- Term limitedAnn Arbor, MIMinimum 1 year directly related experience in clinical research and clinical trials is necessary or an advanced degree in a health-related area 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. Scientific Concepts and Research DesignEthical Participant Safety ConsiderationsInvestigational Products Development and RegulationClinical Study Operations GCPsStudy and Site ManagementData Management and InformaticsLeadership and ProfessionalismCommunication and TeamworkClinical Research Coordinator - AssociateParticipant Screening and RecruitmentExplaining study thoroughly reviewing informed consent answering any questions following GCPIRB and obtaining consent.
Clinical Research Coordinator - Department of Internal Medicine Wayne State UniversityClinical Research Coordinator - Department of Internal MedicineDetroit, MIMay obtain blood samples, including blood draws, cultures, tissues, urine, stool, nasal swabs, plasma, microbiological isolates, and other specimens for laboratory analysis and processing, depending upon the study. The position will work with principal investigators and other research team members to accurately and efficiently carry out a range of tasks associated with a variety of clinical research studies.
Clinical Research Coordinator I/II/III Opportunities - Multiple Locations Nationwide Headlands Research IncClinical Research Coordinator I/II/III Opportunities - Multiple Locations NationwideDetroit, MI$45,000–$100,000 / yearThis general interest posting is designed for experienced Clinical Research Coordinators (CRCs) 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. They play a hands-on role in advancing new therapies, supporting patients through clinical trials, and ensuring studies are conducted with the highest level of quality and care.
MADC Clinical Research Coordinator Associate University of MichiganMADC Clinical Research Coordinator AssociateAnn Arbor, MIWe are seeking an experienced positive highly motivated organized person with excellent multi-tasking ability and record-keeping skills to work with principal investigators and other research team members to accurately and efficiently carry out a range of tasks associated with a variety of research studies. Certification 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.
Assistant Clinical Research Coordinator- Cardiology/Neurology (Detroit, MI) Profound Research LLCAssistant Clinical Research Coordinator- Cardiology/Neurology (Detroit, MI)Detroit, MIAs an Assistant Clinical Research Coordinator at Profound Research, you'll work alongside experienced clinical research staff at one of our sites, supporting the day-to-day execution of clinical trials that give patients access to therapies they couldn't otherwise reach. High school diploma or technical degree with 3+ years of relevant experience in life sciences, OR Associate's degree with 1+ year of relevant experience, OR Bachelor's degree with relevant coursework or experience in a clinical or life sciences setting.
NewRN - Clinical Oncology Research Coordinator- 40 hours- days Henry Ford HospitalRN - Clinical Oncology Research Coordinator- 40 hours- daysDetroit, MICoordinate patient care across multiple departments/ disciplines, ensuring that the treatment adheres to both strict protocol timelines and the critical clinical timeline that is based on the specific patient scenario/diagnosis. GENERAL SUMMARY: Using established procedures, perform assessments independently and in collaboration with the physician investigator to ensure that the objectives of an established oncology research protocol are met and in compliance with IRB and sponsor guidelines.
International Medical Graduate (IMG) - Clinical Research Coordinator Revival Research InstituteInternational Medical Graduate (IMG) - Clinical Research CoordinatorSouthfield, MichiganAdditional 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 AssociateClinical Research Technician University of MichiganClinical Research Coordinator AssociateClinical Research TechnicianAnn 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. 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.
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.
Contractor- Assistant Clinical Research Coordinator (Detroit, MI) Profound Research LLCContractor- Assistant Clinical Research Coordinator (Detroit, MI)Detroit, MIAs an Assistant Clinical Research Coordinator at Profound Research, you'll work alongside experienced clinical research staff at one of our sites, supporting the day-to-day execution of high-volume vaccine clinical trials. High school diploma or technical degree with 3+ years of relevant experience in life sciences, OR Associate's degree with 1+ year of relevant experience, OR Bachelor's degree with relevant coursework or experience in a clinical or life sciences setting.
Clinical Research Coordinator - Technician University of MichiganClinical Research Coordinator - TechnicianAnn Arbor, MIp>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. 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.
Clinical Research Coordinator Assistant - 1 YR Term Limited University of MichiganClinical Research Coordinator Assistant - 1 YR Term LimitedAnn Arbor, MIThe candidate will assist with all aspects of the study design including recruitment, assisting with setting up driving equipment, running a driving simulator, administering cognitive tests, data base management and assistance with materials needed for presentations and manuscripts. Michigan Medicine is comprised of over 30,000 employees and our vision is to attract, inspire, and develop outstanding people in medicine, sciences, and healthcare to become one of the world?s most distinguished academic health systems.
Coordinator Clinical Research McLaren Health Care CorpCoordinator Clinical ResearchFlint, MIp>Position Summary: Responsible for facilitating research studies; providing knowledgeable information regarding each research protocol to the medical and nursing staff; evaluating the eligibility of potential candidates for research studies; assisting in the informed consent process; monitoring research study compliance; collecting and submitting data; coordinating required study procedures to meet protocol requirements and maintain a system for effective data flow. Essential Functions and Responsibilities: Evaluates eligibility of candidates for clinical research studies by reviewing protocol defined eligibility requirements and/or collecting pertinent data on potential candidates, verifying appropriateness of patients for entry to clinical trials, and assisting the other staff in determining eligibility of potential patients.
Cardiology Clinical Research Coordinator Actalent IncCardiology Clinical Research CoordinatorDetroit, MI$26–$29 / hourIf you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market.
Clinical Research Coordinator II McLaren Health Care CorpClinical Research Coordinator IIDetroit, MIDesign systems for coordinating, compiling and submission of data; design workflow processes and participate in quality assurance measures; coordinate site visits. Maintain logs, including tracker submissions and update the CTO Oncore database in a timely manner according to CTO SOPs.
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.
Contractor- Clinical Research Coordinator (Detroit, MI) Profound ResearchContractor- Clinical Research Coordinator (Detroit, MI)Detroit, MichiganOur Mission: Improving Lives by Providing Advanced Therapeutic Options Our Vision: Creating the Absolute Best Patient-Physician Experience in Clinical Research Our Values: Compassion: We prioritize the patient-physician relationship, ensuring every interaction is service-oriented and patient-centered. You’ll help manage study activities, lead participant visits, complete protocol-required procedures and documentation, and work closely with investigators, sponsors, CROs, and internal teams.
CLINICAL CARE COORDINATOR Ambulatory Care Services Rogel Cancer Center Research Nurse University of MichiganCLINICAL CARE COORDINATOR Ambulatory Care Services Rogel Cancer Center Research NurseAnn Arbor, MI$43.10–$67.03 / hourMaintain lab supplies in collaboration with research lab services and data coordinators\n Participate in quality improvement initiatives, study meetings, and research program development\n Provide cross-coverage for research nurses and coordinators as needed\n \n\n \nNursing Specific Info\n \nSalary & Nursing Framework Level:\n \nThis UMPNC RN posting is posted under the Role-Specific Advancement Model (RSAM) as:\n \nCCC- COMPETENT NE.\n \nActual RSAM LEVEL and salary will be determined at time of hire.\n \nRSAM levels range from CCC-COMPETENT NE to CCC-EXPERT NE TO CCC-MASTERY NE or CCC-Mastery Plus NE.\n \nRequired qualifications must be met by the candidate in order to be interviewed and considered for the position. The Research Nurse is required to have a working knowledge of clinical trial protocol requirements and good clinical practices as set forth by federal regulations.\n \nThe ideal candidate for this role is a highly motivated oncology nurse who wants to be at the forefront of cutting-edge cancer research and plays a pivotal role in advancing innovative therapies while delivering exceptional, patient-centered care.\n \nThe Clinical Research Group Research Nurse will be a key driver of clinical trial excellence: blending advanced nursing practice, scientific rigor, and compassionate care to improve outcomes for patients with hematologic malignancies.
Research Study Coordinator II - Cancer Clinical - 40 Hours - Days Henry Ford HospitalResearch Study Coordinator II - Cancer Clinical - 40 Hours - DaysDetroit, MIGENERAL SUMMARY: Under minimal supervision the Research Study Coordinator II: 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.
Contractor- Clinical Research Coordinator (Detroit, MI) Profound Research LLCContractor- Clinical Research Coordinator (Detroit, MI)Detroit, MIDiverse Clinical Exposure: Work across multiple therapeutic areas and study phases, building a breadth of experience that's rare in a single organization (for Clinical / Patient-Facing roles). You'll help manage study activities, lead participant visits, complete protocol-required procedures and documentation, and work closely with investigators, sponsors, CROs, and internal teams.
Clinical Research Coord Assoc University of MichiganClinical Research Coord AssocAnn Arbor, MIThis position will serve as a Clinical Research Coordinator Associate or Clinical Research Coordinator Technician in the Oncology Clinical Trial Support Unit (O-CTSU - Clinic Research Group) in the Rogel Cancer Center, providing study coordination support to faculty and research teams for the University of Michigan Rogel Cancer Center - an NCI-Designated Comprehensive Cancer Center and a member of the National Comprehensive Cancer Network (NCCN). Certification 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 Professional (CCRP) or equivalent.
NewClinical Research Regulatory Associate Actalent IncClinical Research Regulatory AssociateDetroit, MI$25.12–$41.25 / hourThis role focuses on preparing and submitting regulatory documents, coordinating IRB submissions, maintaining study records, and ensuring monitors and study teams have appropriate system access. The Regulatory Associate works closely with Clinical Research Coordinators and Data Coordinators to ensure regulatory compliance, data integrity, and smooth study operations in a collaborative and growth-oriented environment.
NewClinical Research Coord Lead University of MichiganClinical Research Coord LeadAnn Arbor, MIThe CPFRC is a collaborative and collegial program that enjoys the opportunity to partner with many intramural and extramural researchers and includes longitudinal cohorts, clinical trials, health services, and translational research with funding from a variety of sponsors including NIH, industry, and others. The Chronic Pain and Fatigue Research Center (CPFRC), located within the Department of Anesthesiology, is seeking a highly motivated and detailed-oriented Clinical Research Coordinator to provide study coordination for multiple clinical research studies of any complexity.
Clinical Research Coord Inter University of MichiganClinical Research Coord InterAnn Arbor, MI30 - Clinical Coordinator Responsibilities Performs study procedures with accuracy Triages complex study concerns appropriately Schedules prepares for and attends study initiation meetings monitor visits and audits Demonstrates ability to manage increasing levels of protocol complexity andor volume efficiently Leads aortic clinical trials under supervision of Clinical Trial Lead and Clinical Research Manager. 15 - Administrative Responsibilities Provides logistic and regulation guidance on Investigator Initiated Studies for adherence to University and Federal guidelines Provides other administrative support for study activity including management of subject reimbursement and payments Oversees aortic clinical research coordinators Supports study team members on a range of communication and teamwork best practices.
Clinical Research Coord Inter-TERM LIMITED University of MichiganClinical Research Coord Inter-TERM LIMITEDAnn 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 Clinical Research Coordinator will work alongside the Principal Investigator in the Department of Family Medicine and a team of investigators across U-M and another institution to oversee a multi-site federally-funded R01 that will develop an online maternal health toolkit.
Clinical Research Coord Assoc Term Limited University of MichiganClinical Research Coord Assoc Term LimitedAnn 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. 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.
CLINICAL RESEARCH NURSE / COLLEGE OF MEDICINE Central Michigan UniversityCLINICAL RESEARCH NURSE / COLLEGE OF MEDICINESaginaw, MI$70,000–$90,000 / yearClinical responsibilities may include assisting with developing and implementing the activities of a clinical research trial which consists of pre-screening patients for study eligibility and performing delegated study tasks including but not limited to: treatment procedures, drawing blood, performing EKGs, administration and accountability of study medication/study devices, recording adverse events, monitoring patient retention, withdrawals, ethical/legal practices, and audit preparation. This may include the following: creation of drafts for informed consent forms, abstracts, communications with sponsors and/or committees, determination of consent form changes per protocol, amendments, presentation of new study information to the Institutional Review Board-New Study packet, revisions, serious adverse events, protocol deviations, etc.
Research Study Coordinator II- Full time- Cardiovascular Medicine Henry Ford HospitalResearch Study Coordinator II- Full time- Cardiovascular MedicineDetroit, MIli>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. GENERAL SUMMARY: Under minimal supervision, coordinates research projects within guides of regulatory compliance and/or Code of Federal Regulation.
Clinical Research Technician University of MichiganClinical Research TechnicianAnn Arbor, MIRemoteMichigan 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. 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.
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.
Clinical Research Technician Assistant University of MichiganClinical Research Technician AssistantAnn 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.).
Clinical Research Assistant University of MichiganClinical Research AssistantAnn Arbor, MIMay work with regulatory support to collect essential documents and maintain regulatory binder (CVs, MD licenses, lab certifications, IRB rosters, lab norms, etc.); Assists with AEs and SAEs, ORIOS reporting; Uses proper documentation techniques as outlined in the ICH-GCP guidelines.). 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.
Research Study Coordinator I- Full time -Biorepository Research Henry Ford HospitalResearch Study Coordinator I- Full time -Biorepository ResearchDetroit, 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. EDUCATION/EXPERIENCE REQUIRED: Bachelor's degree in a scientific field, Psychology, Sociology, Anthropology or related field.
Research Project Managment I -FRC/SRC Coordinator - Days - New Center One Henry Ford HospitalResearch Project Managment I -FRC/SRC Coordinator - Days - New Center OneDetroit, MIEDUCATION/EXPERIENCE REQUIRED: Bachelor's degree in a related field and five (5) years of relevant experience, including at least two (2) years of research experience; experience leading cross functional teams or a small to moderate sized project. GENERAL SUMMARY: Work closely on one or more moderately complex projects/assignments in collaboration with leadership including the Principal Investigator, Senior Bioscientific Staff, and/or Director or Vice President.
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.
Research Study Coordinator II, CCTRO New Trial Intake Coordinator) - Days - 40 Hours Henry Ford HospitalResearch Study Coordinator II, CCTRO New Trial Intake Coordinator) - Days - 40 HoursDetroit, MIGENERAL SUMMARY: Under minimal supervision, the Research Study Coordinator III, 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.
Clinical Research Nurse RN MyMichigan HealthClinical Research Nurse RNMidland, MichiganThe Clinical Research Nurse works under the guidance and supervision of the Principal Investigator, ensures the integrity and quality of clinical trials are maintained and conducted with federal, state, and local regulations, IRB board approvals, and MyMichigan Health policies and procedures. Provide in service education to the clinical staff of the hospitals (pharmacy, nursing, etc.) related to investigational drugs, devices, or procedures, including physiological effects, drug interactions, side effects, nursing care considerations, etc.
Senior Clinical Research Associate - Oncology Zp Group LlcSenior Clinical Research Associate - OncologyLansing, MIRemote$100,000–$130,000 / yearKeywords: Clinical research associate, CRA, hospital, travel, oncology, documentation, trials, trial sites, cancer, cancer research, GCP, ICH, recruitment plans, projects, project, protocol adherence, regulatory submissions, enrollment, CRF completion, data, data query, start-up phase, phase 1, trial master file, TMF, Investigators site file, ISF, mentorship, Microsoft office, mobile devices. Piper Companies is seeking a well-rounded Senior Clinical Research Associate I with direct oncology monitoring experience to work with a Global CRO.
Clincal Research Coordinator - Technician University of MichiganClincal Research Coordinator - TechnicianAnn Arbor, MIResponsibilities: Assist study team with aspects of clinical research coordination including: identifying potential subjects, screening subjects, consenting and enrolling subjects, and collecting and managing patient and laboratory data for clinical research subjects. Staff members are expected to work independently and regularly exercise good judgment in setting priorities, resolving operational problems, and applying policies, procedures, and methods, while always maintaining the strictest of confidentiality.
RN Clinical Research Corewell HealthRN Clinical ResearchGrand Rapids, MichiganCoordinates and/or performs study activities which may include: respiratory therapy assessments; identification of adverse events; investigational product/test article (drug or device) accountability and administration; collection, processing, and shipment of research specimens; and other research activities to the extent permitted by law and policy. Communicates, collaborates, networks, and acts as a consultant to the study sponsor and/or CRO, research study centers, academic institutions, investigators, physicians/physician offices, ancillary departments, and the multidisciplinary team (including students and residents).
NewClinical Research Specialist Corewell HealthClinical Research SpecialistGrand Rapids, MichiganIdentifies, recruits, screens, and enrolls eligible subjects per protocol; with appropriate training and delegation, performs protocol-required research activities and/or protocol-required research procedures with low clinical complexity (e.g. Coordinates and/or performs study activities which may include: identification of adverse events; assist with management of investigational product/test article (drug or device); collection, processing, and shipment of research specimens; and other research activities to the extent permitted by law and policy.
Research Study Coordinator I-Full time-- Cardiovascular Medicine Henry Ford HospitalResearch Study Coordinator I-Full time-- Cardiovascular MedicineDetroit, 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. EDUCATION/EXPERIENCE REQUIRED: Bachelor's degree in a scientific field, Psychology, Sociology, Anthropology or related field.
NewRegistered Nurse Clinical Coordinator (RN) - Med Surg DMC Harper University/Hutzel Women's HospitalRegistered Nurse Clinical Coordinator (RN) - Med SurgDetroit, MIA specialty referral hospital, Harper has established Centers of Excellence in neurosciences, bariatric surgery, vascular services, multidisciplinary cardiovascular services, hypertension, stroke prevention and heart failure. 4. Coordinates/provides in-service programs to assist staff to maintain or enhance their competence in fulfilling job responsibilities based on identified needs of patient care personnel.
Registered Nurse Clinical Coordinator (RN) - Hemodialysis DMC Harper University/Hutzel Women's HospitalRegistered Nurse Clinical Coordinator (RN) - HemodialysisDetroit, MIA specialty referralhospital, Harper has established Centers of Excellence in neurosciences, bariatricsurgery, vascular services, multidisciplinary cardiovascular services, hypertension,stroke prevention and heart failure. 4. Coordinates/provides in-service programs to assist staff to maintain or enhance their competence in fulfilling job responsibilities based on identified needs of patient care personnel.
Hospital and Clinical Affiliates Curriculum Coordinator - Dept. of Undergraduate Medical Education Wayne State UniversityHospital and Clinical Affiliates Curriculum Coordinator - Dept. of Undergraduate Medical EducationDetroit, MIp>Position Purpose: The Hospital and Clinical Affiliates Curriculum Coordinator will manage and run the required clerkships assigned to the segment 3 (third year, M3) medical students, and will work in concert with and under the guidance of the Associate Dean for Clinical Education and the Director of Undergraduate Medical Education and Curricular Affairs. This position will provide leadership within the clerkships in support of the individual clerkship directors (MD/DO) and the departmental coordinators, the hospitals, and other affiliates, and within the SOM in collaboration with the other administrative areas.