156 Results for

Research Jobs in Waterford, MI

Jobs

Ann Arbor, MI7 days ago

Ideal candidates will possess combinations of clinical and research excellence, leadership abilities and dedication to education, and will bring innovation in clinical care as we create advanced care delivery models. The University of Michigan, Department of Internal Medicine, Division of Metabolism, Endocrinology & Diabetes is a seeking a full-time, board certified/eligible candidate for a faculty position in the rank of Clinical Assistant Professor.

Ann Arbor, MI11 days ago

Please 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.

Detroit, MI30+ days ago

This 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.

Ann Arbor, MI30+ days ago

We are looking for a personable, self-motivated, and organized Clinical Research Assistant to help with participant recruitment and mailing activities for a large, multi-year clinical trial testing the efficacy of behavioral interventions on menthol smoking cessation among a diverse population of adults from six states. At least six months of previous experience in one or more of the following areas: research, clinical/hospital work or volunteer experience, customer service, and/or work experience requiring cold calling or managing a high volume of phone calls.

Ann Arbor, MI18 days ago

Please 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.).

Detroit, Michigan21 days ago

As 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.

Ann Arbor, MI30+ days ago

Minimum 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.

Ann Arbor, MI18 days ago

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. 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.

Detroit, MI30+ days ago

Our 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.

Detroit, MI30+ days ago

Our 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.

Ann Arbor, MI17 days ago

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. 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.

Detroit, MI20 days ago

As 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.

Detroit, MI30+ days ago

As 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.

Ann Arbor, MI30+ days ago

The 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.

Detroit, Michigan13 days ago

The institute is equipped with advanced platforms—including organoid and stem cell models, AI-driven analysis, FACS, and CRISPR technologies—and provides access to extensive shared core facilities. NGNRI supports both in-house researchers and visiting scientists, creating a dynamic, mission-driven ecosystem designed to advance innovation and deliver impact in an underserved field.

Ann Arbor, MI30+ days ago

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. 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.

Royal Oak, MI11 days ago

Under supervision of Chief of MR Rad Imaging Physics in the Department of Radiation Oncology, Corewell Health William Beaumont University Hospital in Royal Oak, the candidate is responsible for data entry and maintaining research data base, MR imaging (MRI) data analysis, consenting and scheduling patients for research MRI studies, retrieving clinical data from electronic medical records, dealing with IRB regulatory issues, supporting manuscript and grant development, and other research activities as assigned by the supervisor. We require a drug-free workplace and require team members to comply with the MMR, Varicella, Tdap, and Influenza vaccine requirement if in an on-site or hybrid workplace category.

Ann Arbor, MI30+ days ago

or An advanced degree in a health-related areas such as Health Sciences Behavioral Sciences Public Health HealthCare Administration Clinical Research Administration Social Work Psychology Epidemiology Foreign MD. or Minimum 3 years of human subject experience clinical lab or health regulations. • Scientific Concepts and Research Design • Ethical Participant Safety Considerations • Investigational Products Development and Regulation • Clinical Study Operations GCPs • Study and Site Management • Data Management and Informatics • Leadership and Professionalism • Communication and Teamwork.

Detroit, MI30+ days ago

Assist principal investigator with writing methods and summarizing/organizing data to be used in preparing and presenting presentations for professional, scientific and academic conferences and submittal to academic and scholarly peer-reviewed journals. 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.

Detroit, MI30+ days ago

Proofread and edit research data and documents to ensure accuracy Assist principal investigator with writing methods and summarizing/organizing data to be used in preparing and presenting presentations for professional, scientific and academic conferences and submittal to academic and scholarly peer-reviewed journals. 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.

Detroit, MI30+ days ago

Detroit, MI10 days ago

Detroit, MI30+ days ago

Assist principal investigator with writing methods and summarizing/organizing data to be used in preparing and presenting presentations for professional scientific and academic conferences and submission to academic and scholarly peer-reviewed journals. 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.

Detroit, Michigan30+ days ago

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. 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.

MI13 days ago

Remote

$97,000–$193,000 Per Year

Typically 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.

Detroit, MI30+ days ago

$45,000–$100,000 Per Year

This 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.

Ann Arbor, MI30+ days ago

Interest in issues of health promotion, personal commitment to high-quality work, excellent communication skills, both oral and written in the English language, attention to detail, strong organizational skills, excellent interpersonal skills, the ability to multi-task and prioritize efforts, the ability to work both as part of a team and individually while meeting deadlines, and a commitment to improving the care and lives of children. Working with a multidisciplinary team and across external study sites throughout the U.S., organizing, developing, and expanding research networks of clinicians, inventing and refining new models of care for patients recovering from critical illness.

Ann Arbor, MI30+ days ago

It is presumed that this position is able to apply their skills to a broad range of different types of clinical studies navigate available resources appropriately effectively use all tools and job aids at their disposal and operate e-clinical technologies with a reasonable degree of proficiency. 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.

Southfield, Michigan12 days ago

Additional 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.

Southfield, Michigan30+ days ago

Detroit, MI13 days ago

The institute is equipped with advanced platforms-including organoid and stem cell models, AI-driven analysis, FACS, and CRISPR technologies-and provides access to extensive shared core facilities. NGNRI supports both in-house researchers and visiting scientists, creating a dynamic, mission-driven ecosystem designed to advance innovation and deliver impact in an underserved field.

Detroit, MI30+ days ago

May 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.

Ann Arbor, MI30+ days ago

Primary job duties include: (1) administer and score cognitive and behavioral test measures, (2) facilitate study visits, (3) enter data into an electronic database, (4) maintain detailed study records, and (4) effectively collaborate with the study?s coordinating center and local Michigan Alzheimer?s The SuperAging Program is seeking a highly motivated, organized individual with excellent record-keeping skills to work in a semi-independent manner to accurately and efficiently carry out a range of tasks associated with the study.

Detroit, MI13 days ago

$108,800–$202,000 Per Year

Relationship Management & Site Support: Builds deep, multi-stakeholder relationships at strategic sites (including investigators, pharmacists, and administration), acting as a "site champion" and Primary Point of Contact to maintain cross-study consistency and address site needs. Cross-Functional Collaboration & Reporting: Partners seamlessly with internal teams (e.g., Medical Affairs, Study Start-Up) and CROs to ensure unified site communication, while maintaining meticulous documentation of site visits and interactions in central systems (e.g., Veeva).

Detroit, MI30+ days ago

Lead, 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.

Ann Arbor, MI14 days ago

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.

Ann Arbor, MI30+ days ago

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. 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.

Detroit, MI30+ days ago

Evaluate 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.

Ann Arbor, MI19 days ago

Responsibilities: 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.

Flint, MI30+ days ago

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.

Detroit, MI30+ days ago

Flexible 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.

Detroit, MI10 days ago

Position 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.

Ann Arbor, MI30+ days ago

The Michigan Biotrust for Health is seeking an organized Research Associate to support the next data collection and recruitment phase for a Multimedia Informed Consent Intervention study conducted throughout multiple sites across Michigan. Michigan Medicine conducts background screening and pre-employment drug testing on job candidates upon acceptance of a contingent job offer and may use a third-party administrator to conduct background screenings.

Detroit, MI30+ days ago

Willing 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.

Detroit, MI30+ days ago

Initiate grant proposals in the areas of survey research and/or program evaluation, including identifying funding sources and RFPs, conducting literature reviews, developing research questions, designing research methods, data analysis plan, and data collection procedures. • Computer-Assisted Telephone Interviewing (CATI) • Work closely with others to set up call center procedures and protocols, including training, monitoring interviewer performance, tracking interviewing hours against numbers of completes, etc.

Detroit, MI10 days ago

EDUCATION/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. 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.

Detroit, MI13 days ago

EDUCATION/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.

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Research Jobs in Waterford, MI

Endocrinology Clinical Assistant Professor University of Michigan

Clinical Research Coord Tech underfill Clinical Research Assistant University of Michigan

Clinical Research Assistant Opportunities - Multiple Locations Nationwide Headlands Research Inc

Clinical Research Assistant University of Michigan

Clinical Research Technician Assistant University of Michigan

Contractor- Assistant Clinical Research Coordinator (Detroit, MI) Profound Research

Clinical Research Coord Tech underfill Asst. University of Michigan

Clinical Research Coordinator AssociateTechnician Assistant- Term limited University of Michigan

Clinical Research Coord Inter-TERM LIMITED University of Michigan

Research Study Coordinator III - Cancer Clinical & Translational Research - 40 Hours - Days Henry Ford Hospital

Research Study Coordinator II - Cancer Clinical and Translational Research Office - 40 Hours - Days Henry Ford Hospital

Clinical Research Coordinator AssociateClinical Research Technician University of Michigan

Contractor- Assistant Clinical Research Coordinator (Detroit, MI) Profound Research LLC

Assistant Clinical Research Coordinator- Cardiology/Neurology (Detroit, MI) Profound Research LLC

Clinical Research Coordinator Assistant - 1 YR Term Limited University of Michigan

Research Assistant Grade II/III Rocket Mortgage

Clinical Research Technician Underfill University of Michigan

Research Assistant Corewell Health

Clinical Research Technician University of Michigan

Research Assistant - Center for Nursing Workforce Wayne State University

Research Assistant - Department of Internal Medicine Wayne State University

Research Assistant - Department of Oncology Wayne State University

Research Assistant - Department of Psychiatry Wayne State University

Research Assistant - Office of Women''s Health Wayne State University

Research Assistant - Department of Ophthalmology, Visual and Anatomical Sciences Wayne State University

Research Assistant - Department of Emergency Medicine Wayne State University

Clinical Research Coordinator- Neurology (Detroit, MI) Profound Research

Senior Clinical Research Associate - CNS/Rare Disease - Midwest - Remote Worldwide Clinical Trials Holdings Inc

Clinical Research Coordinator I/II/III Opportunities - Multiple Locations Nationwide Headlands Research Inc

Clinical Research Coord Inter University of Michigan

Clinical Research Coord Assoc University of Michigan

International Medical Graduate (IMG) - Clinical Research Revival Research Institute

International Medical Graduate (IMG) - Clinical Research Coordinator Revival Research Institute

Research Assistant Grade II/III Rocket Companies Inc

Clinical Research Coordinator - Department of Internal Medicine Wayne State University

SuperAging Research Assistant 2 yr Term limited University of Michigan

Clinical Research Engagement Lead - Northeast Region (Detroit, MI) Genentech Inc

Clinical Research Coordinator (Detroit, MI) Profound Research LLC

Clinical Research Technician Temporary University of Michigan

Clinical Research Coord Assoc Term Limited University of Michigan

Post-Doctoral Fellow/Research Associate - Department of Oncology Wayne State University

Clincal Research Coordinator - Technician University of Michigan

Coordinator Clinical Research McLaren Health Care Corp

Clinical Research Associate II ICON Plc

Clinical Research Registered Nurse McLaren Health Care Corp

RESEARCH ASST II TEMP University of Michigan

Clinical Research Associate - Oncology - Detroit ICON Plc

Research Assistant Wayne State University

Research Project Mgmt I- Full time- Center for Health Services Henry Ford Hospital

Research Project Managment I -FRC/SRC Coordinator - Days - New Center One Henry Ford Hospital

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