340 Results for

Clinical Jobs in Redford, MI

Jobs

Canton, MI7 days ago

$100,000–$130,000 Per Year

We are a rapidly growing, BCBA-founded ABA organization committed to delivering compassionate, outcomes-driven autism services across center-based, home-based, school, and community settings. The Clinical Director will partner closely with executive leadership to drive clinical excellence, improve operational outcomes, mentor BCBA Supervisors, and support the continued expansion of services to families across assigned regions.

Canton, MI8 days ago

With Home Program Manager staff meetings at least monthly or as needed to keep patient care staff informed of changes in patient care needs or operations to improve delivery of care. Approve or disapprove time or personnel schedule changes in the absence on the Home Therapy Manager ensuring compliance with applicable regulations, policies and procedures for documenting time of work hours for staff members on assigned shift.

New!

Ann Arbor, MI2 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.

New!

Eastpointe, MIToday

$238,832–$341,189

For patients that are unable to come to the office—in hospital, SNF, LTC or homebound, engages with the transitional care team and others including case managers, acute and transitional-care physicians, and other resources that may be available depending on the market. Leads Super Huddle (SH) and Transforming Care Meeting (TCM) weekly, as well as supports Center Manager/Center General Manager center clinical leader and/or market clinical leader is not available, based on guidance from Market Chief Medical Officer.

New!

Eastpointe, MIToday

$238,832–$341,189

New!

Eastpointe, MIToday

$238,832–$341,189

New!

Eastpointe, MIToday

$238,832–$341,189

New!

Eastpointe, MIToday

$238,832–$341,189

New!

Garden City, MIToday

$156,600–$266,700

Risks 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.

New!

Garden City, MIToday

$156,600–$266,700

New!

Garden City, MIToday

$156,600–$266,700

New!

Garden City, MIToday

$156,600–$266,700

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.

MI8 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.

New!

Ann Arbor, MI6 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.

Ann Arbor, MI13 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.).

Ann Arbor, MI13 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.

Ann Arbor, MI30+ days ago

The Center?s mission is to optimize cardiometabolic health and reduce cardiovascular risk across the health system through a data science-driven, risk-based approach spanning six integrated cores: Population and Data Science, Phenotyping, Cardiometabolic Health Clinic and Clinical Trials, Health System Implementation, Industry and Academic Partnerships, and Training and Education. The Clinical Research Program Manager will serve as the operational backbone of this multidisciplinary clinical research enterprise, providing administrative and scientific coordination across active clinical trials, observational studies, and translational research initiatives.

Ann Arbor, MI20 days ago

Remote

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.

Garden City, Michigan14 days ago

Participates 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).

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.

Warren, Michigan30+ days ago

PhD/PharmD in a relevant scientific discipline with a minimum of 5 years of progressively responsible experience in a pharmaceutical, biotechnology or related environment OR equivalent combination of experience and education. The Senior Manager, Clinical Pharmacology conducts pharmacokinetic/toxicokinetic studies to support preclinical and clinical development of novel therapies and life cycle management.

Dearborn, MI13 days ago

$66,800–$125,000 Per Year

Essential Functions: Monitors investigator sites with a risk-based monitoring approach: applies root cause analysis (RCA), critical thinking and problem-solving skills to identify site processes failure and corrective/preventive actions to bring the site into compliance and decrease risks. May need to maintain regular contact between monitoring visits with investigative sites to confirm that the protocol is being followed, that previously identified issues are being resolved and that the data is being recorded in a timely manner.

New!

Warren, Michigan3 days ago

May be assigned unmasked tasks for studies, which may include but is not limited to, assisting with masked investigational product, set up and management of unmasked trial master file, review of unmasked data in the electronic data capture system, point of contact for IVRS issues, and support oversight of unmasked clinical monitoring. Oversees and provides input to the development of study specific documentation including but not limited to: case report forms (CRF), data management plan, monitoring plan, monitoring oversight plan, project specific training plan, data review plan, statistical analysis plan, etc.

Warren, Michigan9 days ago

Assigns tasks to Clinical Study Management staff and supports their deliverables; directly supervises CTM staff (work assignments, performance management, recruitment, professional development, coaching, mentoring, ongoing training and compliance, and study support/oversight); recommends and participates in cross-functional and departmental process improvements; and identifies innovative, globally informed approaches to study execution and continuous improvement of CTM SOPs. Leads the cross-functional study team responsible for clinical study delivery, serving as the primary point of contact for leadership and oversight, and oversees execution against planned timelines, deliverables, and budget while raising issues (conduct, quality, timelines, budget) to the Program Operations Lead and stakeholders and implementing corrective actions.

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.

Warren, Michigan10 days ago

Manage CTM inspection action items throughout the inspection lifecycle, from pre-inspection activities (readiness meetings, Q&As, storyboards, presentation requests with internal/CRO stakeholders) to post-inspection tasks (remediation plans, timelines, documentation, closure updates), ensuring prompt resolution and a complete audit trail. This role is expected to leverage Artificial Intelligence (AI)-powered tools — including large language model (LLM) applications such as Claude — to accelerate deliverable production, strengthen documentation quality, and drive continuous improvement in inspection readiness operations, with all AI-assisted outputs subject to human review and full GCP compliance.

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.

Detroit, Michigan16 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.

Southfield, Michigan30+ 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, Michigan7 days ago

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.

Warren, Michigan30+ days ago

This involves supporting Clinical Trial Managers (CTMs) with activities related to: study start-up; investigator site feasibility and selection; essential document review related to investigator site initiation and investigational product release and patient enrollment. Performing periodic ad hoc, interim and end-of-study reviews/audits on paper and electronic TMFs for several trials to ensure TMF meets sponsor’s expectations (includes TMF reconciliation at study close-out).

Ann Arbor, MI30+ days ago

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, MI9 days ago

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

$124,000–$280,000 Per Year

Examples of the skills, knowledge, and experiences you need to lead and deliver value at this level include but are not limited to: • Craft and convey clear, impactful and engaging messages that tell a holistic story. PwC does not intend to hire experienced or entry level job seekers who will need, now or in the future, PwC sponsorship through the H-1B lottery, except as set forth within the following policy: https://pwc.to/H-1B-Lottery-Policy.

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

We 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.

Detroit, Michigan9 days ago

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).

New!

Detroit, MI5 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

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.

Warren, Michigan10 days ago

Acts as medical expert and leader in interactions with external collaborators (e.g., regulatory authorities, key opinion leaders, advisory boards, patient advocacy groups), internal collaborators (e.g., Research, Early Clinical Development, Global Medical Affairs, Marketing, HEOR), and internal decision boards. This role requires an impactful and highly hard-working individual who serves as a clinical role model for the team and demonstrates outstanding clinical scientific knowledge applicable to hematology clinical research.

Warren, Michigan10 days ago

The Medical Director, Clinical Sciences, Oncology is a qualified physician scientist with exceptional academic clinical trials' experience, preferably in solid tumor Oncology drug development. The Medical Director drafts designs of clinical study concepts which lead to clinical trial protocols and is responsible for medical/scientific supervision of individual clinical trials.

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, MI30+ days ago

SABER clinical study monitors provide independent oversight of study conduct and collaborate with project managers, principal investigators, and coordinating center leadership to ensure compliance and alignment across study activities. Work experience in monitoring clinical trials in an academic or industry setting, including monitoring compliance with research regulations and supporting or participating in FDA inspections and audits (desired).

Southfield, MI30+ days ago

The hospital features a 25-bed Acute Psychiatric Care Unit, providing comprehensive inpatient behavioral health services for adults ages 18 and older, and is the only hospital within the health system to receive a 4-Star CMS Quality Rating. Additionally, U.S. News & World Report recognized the hospital as a High Performer (Top 10%) in Adult Specialty rankings for Gastroenterology & GI Surgery and Orthopedics (2025-2026), based on reputation, patient outcomes, safety, and structural measures.

Southfield, MI29 days ago

Resume Resources

Free Resume Templates Free Resume Builder

Get noticed by top employers!

Upload your resume to let employers know you're open to Clinical job opportunities. Plus, receive relevant job recommendations in your inbox.

Create A Free Account

Clinical Jobs in Redford, MI

Clinical Director BCBA Jobot

Clinical Coordinator - Charge Registered Nurse - Dialysis Fresenius Medical Care

Endocrinology Clinical Assistant Professor University of Michigan

Associate Clinical Manager ChenMed

Clinical Manager ChenMed

Associate Chief Clinical Officer ChenMed

Associate Center Clinical Director ChenMed

Chief Clinical Officer ChenMed

Principal Investigator (Neurology) Professional Case Management

Principal Investigator (Pediatrics) Professional Case Management

Principal Investigator (Psychiatry) Professional Case Management

Principal Investigator (Gastroenterology) Professional Case Management

Clinical Research Coord Inter University of Michigan

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

Clinical Research Coord Tech underfill Clinical Research Assistant University of Michigan

Clinical Research Technician Assistant University of Michigan

Clinical Research Coord Inter-TERM LIMITED University of Michigan

Clinical Research Program Manager University of Michigan

Clinical Research Technician University of Michigan

Clinical Research Coordinator Act for Health

Clinical Research Coordinator AssociateTechnician Assistant- Term limited University of Michigan

Senior Manager, Clinical Pharmacology PTC Therapeutics

Clinical Research Associate II - Oncology, Neurology, Ophthalmology (MN, WI, IN, MI, OH) Thermo Fisher Scientific Inc

Senior Manager, Clinical Study Lead, Internal Medicine Regeneron Pharmaceuticals

Senior Manager, Clinical Study Lead Regeneron Pharmaceuticals

Manager, Clinical Study Lead Regeneron Pharmaceuticals

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

Senior Manager Clinical Study Inspection Readiness Regeneron Pharmaceuticals

Clinical Research Coord Assoc University of Michigan

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

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

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

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

Contract, Clinical Trial Associate PTC Therapeutics

Clinical Research Coord Tech underfill Asst. University of Michigan

Clinical Research Coordinator (Detroit, MI) Profound Research LLC

Clinical Research Technician Temporary University of Michigan

Clinical Research Coord Assoc Term Limited University of Michigan

Payer STARS/Quality Clinical Consultant, Senior Manager PricewaterhouseCoopers LLP

Clinical Research Coordinator - Department of Internal Medicine Wayne State University

MADC Clinical Research Coordinator Associate University of Michigan

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

Clinical Research Registered Nurse McLaren Health Care Corp

Clinical Research Technician Underfill University of Michigan

Executive Medical Director, Clinical Development, Hematology Cell Therapy Regeneron Pharmaceuticals

Medical Director, Clinical Development, Oncology (Lung, Breast, Colorectal, Gastric Cancers) Regeneron Pharmaceuticals

Clinical Research Assistant University of Michigan

Clinical Study Monitor University of Michigan

Assistant Clinical Manager, Registered Nurse, Cardiac Stepdown Intermediate Care - Full Time Henry Ford Hospital

Assistant Clinical Manager, Registered Nurse, Stepdown Intermediate Care- Full Time Henry Ford Hospital

Resume Resources