262 Results for

Clinical Jobs in New Baltimore, MI

Jobs

New!

Warren, Michigan3 days ago

The 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.

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.

MI15 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.

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).

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, 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, MI28 days ago

$150,500–$245,500 Per Year

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, MI30+ days ago

$128,600–$210,000 Per Year

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. As a Manager, Clinical Study Lead, a typical day may include the following: 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 escalating issues (conduct, quality, timelines, budget) to the Program Operations Lead and stakeholders and implementing corrective actions.

Warren, Michigan7 days ago

Dearborn, MI20 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.

Warren, Michigan17 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.

Detroit, Michigan23 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, Michigan14 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.

MI30+ days ago

$105,000–$145,000 Per Year

Any unsolicited resumes sent to Zoetis from a third party, such as an Agency recruiter, including unsolicited resumes sent to a Zoetis mailing address, fax machine or email address, directly to Zoetis employees, or to Zoetis resume database will be considered Zoetis property. You will deliver pilot and pivotal clinical studies that support product registrations and provide expertise in companion animal medicine and study conduct to research and development phase projects.

New!

Detroit, MI2 days ago

$25.12–$41.25 Per Hour

This role focuses on preparing and submitting regulatory documents, coordinating IRB submissions, maintaining study records, and ensuring monitors and study teams have appropriate system access. The Regulatory Associate works closely with Clinical Research Coordinators and Data Coordinators to ensure regulatory compliance, data integrity, and smooth study operations in a collaborative and growth-oriented environment.

Detroit, MI23 days ago

Under limited direction, and according to established policies and procedures, provides clinical pharmacy services including primary and consultative services to patients and health care providers to ensure optimal drug utilization in assigned specialty area. A specialty referral hospital, Harper has established Centers of Excellence in neurosciences, bariatric surgery, vascular services, multidisciplinary cardiovascular services, hypertension, stroke prevention and heart failure.

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.

Detroit, MI30+ days ago

li>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.

Detroit, MI15 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, MI28 days ago

$197,000–$295,000 Per Year

In addition, our positions offer a short-term incentive bonus opportunity; eligibility to participate in our equity-based long-term incentive program (salaried roles), to receive a retirement contribution (hourly roles), and commission payment eligibility (sales roles). Capture applicable field insights (feasibility, operational bottlenecks, patient pathways) and deliver them to global and local partners to lead early risk identification and inform protocol/process adjustments.

Warren, Michigan17 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, Michigan17 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.

Detroit, MI12 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.

Bingham Farms, MI17 days ago

$93,500–$115,000 Per Year

As a Home Health Clinical Manager, you'll oversee the coordination and quality of care for patients throughout their home health journey, ensuring they receive the right care at the right time while supporting positive outcomes and an exceptional patient experience. You'll provide leadership, mentorship, and clinical guidance to a multidisciplinary team of nurses, therapists, social workers, and home health aides while fostering a culture of collaboration, accountability, and continuous improvement.

Clinton Township, Michigan15 days ago

Remote

This role oversees clinical outcomes, coordinates quality initiatives, ensures adherence to regulations, and collaborates with the interdisciplinary team to drive continuous improvement in patient safety and clinical quality performance. Collaborate with physicians, nurses, dietitians, social workers, and leadership to support evidence-based clinical initiatives.

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, MI30+ days ago

li>

Southfield, MI30+ days ago

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. 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.

Southfield, MI30+ days ago

li>

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.

Detroit, MI22 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, Michigan30 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. ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

Detroit, Michigan30 days ago

ICON 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.

Troy, MI30+ days ago

Full-time

Southfield, MI30+ days ago

Full-time

Detroit, MI30+ days ago

li>

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, 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.

New!

Detroit, MI6 days ago

Coordinate 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.

Detroit, MI16 days ago

$26–$29 Per Hour

If 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.

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.

Dearborn, MI19 days ago

Experience as a CEAP or EAP internal/external consultant to a work site area required (for the integrated unit only), or A minimum of 2 years' experience, prior to licensure with Carelon Behavioral Health Options Clinical Operations Unit functioning as a Clinical Support Specialist with required licensure activities supervised by the Clinical Manager or Clinical Director. Evaluates clinical appropriateness of treatment using professional knowledge within Carelon Behavioral Health Options clinical and work site guidelines and renders certification decisions or seeks consultations for non-certification decisions.

Southfield, MI30+ days ago

The Manager, Clinical Informatics develops, organizes, directs, evaluates, and promotes informatics functions and initiatives in implementing and utilizing the Electronic Health Record (EHR) technology to improve the quality and accessibility of healthcare, increase clinician EHR efficiencies, designing and validating clinical databases, creating procedures to handle data management, data entry and processing, including electronic health record transfers and maintenance, increase patient participation and satisfaction, improve the accuracy of diagnoses and health outcomes, and to realize efficiencies and costs savings (e.g., streamlined coding and billing procedures). This includes working collaboratively and effectively with operational and medical leadership, multiple disciplines, quality, system performance improvement teams, and committees to plan and implement changes in organizations; facilitating problem-solving processes (e.g., identifying issues and outlining action plans); and assisting leaders with planning and assessments.

Dearborn, Michigan20 days ago

Two years of demonstrated informal leadership experience for internal candidates, which may include roles such as Charge Nurse, Lead Nurse, or participation in Shared Governance Councils. This role provides leadership and oversight of patient care staff to support a culture of excellence in clinical practice, staff engagement, recruitment and retention, and strong clinical and operational outcomes.

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Clinical Jobs in New Baltimore, MI

Senior Manager Clinical Study Lead (Clinical Experimental Sciences) Regeneron Pharmaceuticals

Senior Manager, Clinical Pharmacology PTC Therapeutics

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

Contract, Clinical Trial Associate PTC Therapeutics

Payer STARS/Quality Clinical Consultant, Senior Manager PricewaterhouseCoopers LLP

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

Senior Manager, Clinical Study Lead Regeneron Pharmaceuticals Inc

Manager, Clinical Study Lead Regeneron Pharmaceuticals Inc

Senior Manager, Clinical Study Lead, Internal Medicine Regeneron Pharmaceuticals

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

Senior Manager Clinical Study Inspection Readiness Regeneron Pharmaceuticals

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

Clinician, Companion Animal Clinical Development Zoetis Inc

Clinical Research Regulatory Associate Actalent Inc

Clinical Pharmacist Specialist Full Time Days DMC Harper University/Hutzel Women's Hospital

Clinical Research Coordinator (Detroit, MI) Profound Research LLC

Clinical Research Coordinator - Department of Internal Medicine Wayne State University

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

Field Clinical Advisor - Cell Therapy - OH/MI AstraZeneca Plc

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

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

Clinical Research Registered Nurse McLaren Health Care Corp

Home Health RN Clinical Manager - $10,000 Sign On Bonus! Optimal Care

Strategic Clinical Quality Manager - Michigan Region Fresenius Medical Care

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

Assistant Clinical Manager, Registered Nurse, Labor and Delivery/NICU- Full Time Henry Ford Hospital

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

Assistant Clinical Manager, Registered Nurse, Med Surg Neuro Trauma - Full Time Henry Ford Hospital

Assistant Clinical Manager, Registered Nurse, ICU - Full Time Henry Ford Hospital

Assistant Clinical Manager, Registered Nurse, Acute Rehab - Full Time Henry Ford Hospital

Assistant Clinical Manager, Registered Nurse, Cardiac ICU - Full Time Henry Ford Hospital

Assistant Clinical Manager, Registered Nurse - Stepdown Intermediate Care/Med Surg Nephrology Care Unit - Full Time Henry Ford Hospital

Assistant Clinical Manager, Registered Nurse, Emergency Department - Full Time Henry Ford Hospital

Clinical Research Assistant Opportunities - Multiple Locations Nationwide Headlands Research Inc

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

Clinical Research Associate IRE

Clinical Research Associate II IRE

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

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

Clinical Research Associate II ICON Plc

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

RN - Clinical Oncology Research Coordinator- 40 hours- days Henry Ford Hospital

Cardiology Clinical Research Coordinator Actalent Inc

Clinical Research Associate - Oncology - Detroit ICON Plc

Clinical Care Manager II (Union) - Michigan Licensed Elevance Health Inc

Clinical Informatics Manager Corewell Health

Clinical Nurse Manager NICU Corewell Health

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