NewPrincipal Investigator (Gastroenterology) Professional Case ManagementPrincipal Investigator (Gastroenterology)Garden City, MI$156,600–$266,700Risks 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.
NewPrincipal Investigator (Pediatrics) Professional Case ManagementPrincipal Investigator (Pediatrics)Garden City, MI$156,600–$266,700Risks 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.
NewPrincipal Investigator (Psychiatry) Professional Case ManagementPrincipal Investigator (Psychiatry)Garden City, MI$156,600–$266,700Risks 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.
NewPrincipal Investigator (Neurology) Professional Case ManagementPrincipal Investigator (Neurology)Garden City, MI$156,600–$266,700Risks 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.
NewPerm - Physician - Hematology Oncology Detroit, MI VieMed Healthcare StaffingPerm - Physician - Hematology Oncology Detroit, MIDetroit, MI$500,000–$550,000 / yearThe role involves strategic oversight of clinical, academic, and research programs in Hematology/Oncology, with an emphasis on growth, innovation, and excellence. Experience: Proven leadership experience in an academic or large health system setting; prior oversight of faculty, clinical, and research programs.
Senior Clinical Research Associate - CNS/Psychiatry - Midwest (Remote) Worldwide Clinical Trials Holdings IncSenior Clinical Research Associate - CNS/Psychiatry - 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.
Senior Clinical Research Associate - CNS/Rare Disease - Midwest - Remote Worldwide Clinical Trials Holdings IncSenior Clinical Research Associate - CNS/Rare Disease - Midwest - RemoteMIRemote$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.
Clinical Research Associate II ICON PlcClinical Research Associate IIDetroit, MIFlexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others. Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family's well-being.
Clinical Research Associate II IREClinical Research Associate IIDetroit, MichiganICON 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.
Clinical Research Coordinator Act for HealthClinical Research CoordinatorGarden City, MichiganParticipates in recruitment of participants to include personally engaging the general public face to face in local across hard-to-reach communities, attending community events, speaking with physicians and people across diverse cultures and backgrounds to support meeting participant enrollment targets . Ensures adherence to clinical trial protocols and supports the clinical trials team in ensuring that trials are conducted and comply with all regulatory, state, national and internationally accepted guidelines for Good Clinical Practice (ICH GCP).
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 Associate IREClinical Research AssociateDetroit, MichiganWilling and able to travel up to 50% for on-site monitoring visits across Midwest region; preference given to candidates residing in Detroit near major HUB airports to support efficient regional travel. ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
Clinical Research Associate - Oncology - Detroit ICON PlcClinical Research Associate - Oncology - DetroitDetroit, MIWilling and able to travel up to 50% for on-site monitoring visits across Midwest region; preference given to candidates residing in Detroit near major HUB airports to support efficient regional travel. Life assurance Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.
NewClinical Research Associate II Allen SpoldenClinical Research Associate IIOakland, MichiganConduct ongoing study monitoring, including frequent periodic site visits, protocol adherence checks, material handling procedures, inspection of study files, and related monitoring functions. Initiate studies performing initiation site visits, arrange for shipment of clinical supplies, case report forms, and other necessary materials.
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.
RN - 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.
RN - Clinical Oncology Research Coordinator Leader- 40 hours- days Henry Ford HospitalRN - Clinical Oncology Research Coordinator Leader- 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 which 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.
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 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.
NewClinical Research Data Coordinator Actalent IncClinical Research Data CoordinatorDetroit, MI$27–$33.65 / hourWorking closely with data, clinical, regulatory, and nursing colleagues, this role ensures accurate, timely, and compliant data management for oncology and hematology clinical research studies while contributing to a collaborative and growth-oriented environment. The Clinical Data Coordinator supports a hematology-focused research team by managing clinical data throughout its lifecycle, from collection in the electronic medical record (EMR) to upload, query resolution, and audit preparation.
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.
Clinical Research Registered Nurse McLaren Health Care CorpClinical Research Registered NurseDetroit, MIPosition Summary: The CRN is a member of the clinical research team and assists in the recruitment, compliance and follow-up of patients that are eligible for, or registered to a clinical trial. The CRN provides specialized nursing care that ensures exceptional, ethical, safe care yielding high-quality data.
Senior Analyst - Financial - Clinical Research - FT - Days - MHS South Broward Hospital DistrictSenior Analyst - Financial - Clinical Research - FT - Days - MHSMIRequired Work Experience: Three (3) years experience with coverage analysis, clinical trial budget development and negotiation, clinical research study coordination or management, health system operations, or other related research or healthcare experience. Responsibilities:Performs comprehensive and independent analysis of clinical trial protocols and other study documents, including the research study budget, contract, informed consent, pharmacy and lab manuals, and other supporting documentation.
International Medical Graduate (IMG) - Clinical Research Revival Research InstituteInternational Medical Graduate (IMG) - Clinical ResearchSouthfield, 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.
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 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).
Assoc-Research-Clinical- Part time 24 --Henry Ford Providence Hospital Henry Ford HospitalAssoc-Research-Clinical- Part time 24 --Henry Ford Providence HospitalSouthfield, MICollects, prepares and maintains required research documentation, such as informed consent records, case records, clinical notes and medical reports. Assists with the preparation and delivery of internal and external presentations, conference reports and lectures, and publishing submissions.
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 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.
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.
International Medical Graduate (IMG) - Clinical Research Revival Research Institute, LLCInternational Medical Graduate (IMG) - Clinical ResearchSouthfield, 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.
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.
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 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.
Sub-Investigator/Advanced Practice Provider, Clinical Trials Research SRI InternationalSub-Investigator/Advanced Practice Provider, Clinical Trials ResearchPlymouth, Michigan$43.47–$61 / hourOverview: SRI's Clinical Trials Unit is seeking an experienced Sub-Investigator (Sub-I)/Nurse Practitioner with a background as an Advanced Practice Provider (APP) for a part-time, temporary role in clinical trials research. Serve as a clinical liaison between research participants, investigators, sponsors, and healthcare providers to support participant safety and study quality.
Sub Investigator/Advanced Practice Provider, Clinical Trials Research SRI InternationalSub Investigator/Advanced Practice Provider, Clinical Trials ResearchPlymouth, MI$43.47–$61 / hourSRI''s Clinical Trials Unit is seeking an experienced Sub-Investigator (Sub-I)/Nurse Practitioner with a background as an Advanced Practice Provider (APP) for a part-time, temporary role in clinical trials research. Serve as a clinical liaison between research participants, investigators, sponsors, and healthcare providers to support participant safety and study quality.
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.
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.
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.
NewResearch 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.
Faculty Research Integration Lead-HFH+MSU Partnership Henry Ford HospitalFaculty Research Integration Lead-HFH+MSU PartnershipDetroit, MIEDUCATION/EXPERIENCE REQUIRED: Bachelor's degree in a related field and seven (7) years of relevant experience, including at least three (3) years of research experience; experience leading cross functional teams or a small to moderate sized project OR Master's degree in a related field with two (2) years of relevant experience and competency, including at least one (1) year of research experience. We are seeking a highly organized, proactive, and collaborative Faculty Research Integration Lead to support the successful relocation, onboarding, and integration of new research faculty into the Henry Ford Health + Michigan State University Health Sciences (HF+MSU) partnership.
Research Associate - Department of Physical Medicine & Rehab Wayne State UniversityResearch Associate - Department of Physical Medicine & RehabDetroit, MIEvaluate and perform data analysis using graphs, charts or tables to highlight the key points of the research results collected in accordance with the research protocols as stipulated. Design and perform research protocols independently or as directed through training in more difficult or specialized procedures to meet the needs of the research protocol.
Research Associate - Department of Oncology Wayne State UniversityResearch Associate - Department of OncologyDetroit, MIEvaluate and perform data analysis using graphs, charts, or tables to highlight the key points of the research results collected in accordance with the research protocols as stipulated. Design and perform experiments, recruit participants for studies by developing surveys and interviewing candidates.
Research Associate - Department of Ophthalmology, Visual and Anatomical Sciences Wayne State UniversityResearch Associate - Department of Ophthalmology, Visual and Anatomical SciencesDetroit, MIEvaluate and perform data analysis using graphs, charts or tables to highlight the key points of the research results collected in accordance with the research protocols as stipulated. Job Purpose: Under the direction of the Principal Investigator, provide scientific and technical assistance to complete laboratory based, clinical or population science research.
Post-Doctoral Fellow/Research Associate - Department of Oncology Wayne State UniversityPost-Doctoral Fellow/Research Associate - Department of OncologyDetroit, MIEvaluate and perform preliminary analysis of the data using graphs, charts or tables to highlight the key points of the research results collected in accordance with the research protocols as stipulated. Evaluate and perform data analysis using graphs, charts or tables to highlight the key points of the research results collected in accordance with the research protocols as stipulated.
Research Project Manager Actalent IncResearch Project ManagerDetroit, MI$43.50–$53 / 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.
RN - Nurse Manager-Oncology Research- 40 hours- days Henry Ford HospitalRN - Nurse Manager-Oncology Research- 40 hours- daysDetroit, MIProvides clinical leadership and works in partnership with nursing, the health care team, and leadership to assure quality patient care provided in accordance with departmental, Henry Ford Medical Group and health system policies and procedures. GENERAL SUMMARY: Under the leadership of a Vice President, Director, Group Practice Director and/or Physician Leadership, the individual in this position focuses on activities associated with clinical research operations.
Medical Director of Research- Infectious Disease Henry Ford HospitalMedical Director of Research- Infectious DiseaseDetroit, MIHenry Ford Health in Detroit, Michigan is seeking a Board Certified Infectious Diseases physician to serve as Medical Director of Infectious Disease Research, leading a nationally respected division with a long history of excellence in clinical care, education, and scientific innovation. This academic leadership role offers the opportunity to shape the division's research strategy, oversee clinical trials and translational studies, foster interdisciplinary collaborations, mentor faculty and trainees, and guide grant development across NIH, CDC, and industry funded portfolios.
Senior Manager Clinical Study Lead (Clinical Experimental Sciences) Regeneron PharmaceuticalsSenior Manager Clinical Study Lead (Clinical Experimental Sciences)Warren, MichiganThe CES Ops portfolio is dynamic in nature; study types include, but are not limited to, less complex data transfer agreements, retrospective sample/data acquisition studies to more complex prospective studies including sample/data acquisition, biomarker/technology/method validation, genotypic/phenotypic call back studies, and challenge/screening studies. The Senior Clinical Study Lead (CSL) – Clinical Experimental Sciences Operations (CES Ops) is accountable for the execution of assigned clinical studies/research collaborations from study design, through execution, to study close out.
Postdoctoral Fellow (Lung and Ovarian Cancers Research) - 40 Hours - Days Henry Ford HospitalPostdoctoral Fellow (Lung and Ovarian Cancers Research) - 40 Hours - DaysDetroit, MIGENERAL SUMMARY: Under the direction of a senior investigator design, executes, analyzes, and interprets various laboratory experiments with a focus on current scientific questions, as identified by the senior scientists. Our lab focuses on uncovering the molecular mechanisms of cancer development, metabolic reprogramming and therapy resistance, with the ultimate goal of identifying combinatorial strategies for improving treatment outcome.