NewClinical Research Associate II Inspire Medical Systems Inc.Clinical Research Associate IIMinneapolis, MN$85,000–$105,000 / yearPerform remote and on-site monitoring visits at participating clinical study centers to ensure the safety of study patients, the reporting of accurate study data and appropriate study management at the clinical study center. Applicants with a disability that need accommodation to complete the Inspire Medical Systems application process should contact Human Resources at 844-672-4357 or email careers@inspiresleep(dot)com .
NewClinical Research Associate II Inspire Medical Systems IncClinical Research Associate IIMinneapolis, MN$85,000–$105,000 / yearPerform remote and on-site monitoring visits at participating clinical study centers to ensure the safety of study patients, the reporting of accurate study data and appropriate study management at the clinical study center. Applicants with a disability that need accommodation to complete the Inspire Medical Systems application process should contact Human Resources at 844-672-4357 or email careers@inspiresleep(dot)com.
NewClinical Research Coordinator (Research Professional 2) University of MinnesotaClinical Research Coordinator (Research Professional 2)Minneapolis, MN$25–$33.65 / hourLocated at the heart of one of the nations most vibrant, diverse metropolitan communities, students on the campuses in Minneapolis and St. Paul benefit from extensive partnerships with world-renowned health centers, international corporations, government agencies, and arts, nonprofit, and public service organizations. The Bronstein lab in the University of Minnesota Department of Psychiatry and Behavioral Sciences is seeking a part-time (20 hours per week) Clinical Research Coordinator (Research Professional 2) for a project which focuses on personalized, non-invasive neuromodulation to improve mental health outcomes.
Senior Clinical Research Monitor Integrated Resources, IncSenior Clinical Research MonitorMounds View, MinnesotaFull timeThis position works under minimal supervision, working closely with study teams, site personnel, and Healthcare field personnel and monitoring supervisor for resolution of site issues.· general therapeutic area education and training)Physical Job Requirements• The physical demands described within the Responsibilities section of this job description are representative of those that must be met by an employee to successfully perform the essential functions of this job.
Clinical and Research Post-Doctoral Associate - Raptor and Wildlife Health University of MinnesotaClinical and Research Post-Doctoral Associate - Raptor and Wildlife HealthMinneapolis, MN$62,232–$65,000 / yearDevelop studies focusing on current wildlife health priorities, potentially including but not limited to: clinical outcomes, wildlife epidemiology, environmental toxicology (e.g., PFAS), post-release monitoring, and climate change impacts. Located at the heart of one of the nations most vibrant, diverse metropolitan communities, students on the campuses in Minneapolis and St. Paul benefit from extensive partnerships with world-renowned health centers, international corporations, government agencies, and arts, nonprofit, and public service organizations.
Clinical Research Specialist Integrated Resources, IncClinical Research SpecialistMounds View, MinnesotaContractorClinical Research SpecialistINTEGRATED RESOURCES STAFFING PVT LTDJob DescriptionJob Title: Clinical Research SpecialistLocation: Mounds View, MN Duration: 6 + months (Possibility of extension) Local candidate needed on site. Travel: N/A Site: USA-MN-Mounds View Shift Type: FirstPosition ResponsibilitiesOversight of a clinical study including enrolment, long-term follow-up, trial master file maintenance and study activation phases.
Clinical Research Specialist III Integrated Resources, IncClinical Research Specialist IIIMounds View, MinnesotaFull timeMain duties of project are as follows: · Extensive review of Trial Master File and Site Files to ensure files are complete, accurate and compliant with ISO14155, applicable FDA Code of Federal Regulations, project plans and MDT internal SOPs.· Critical review of target records, to identify any audit risks; recommend or take action to mitigate risks· Document file review, all findings and actions as a deliverable to the Clinical Trial ManagerExperience required: 5 plus yearsE ducational: Bachelor's degree required. Job DescriptionJob Title: Clinical Research Specialist IIILocation: Mounds View, MN Duration: 4+ Months (Possibility of extension) Job Roles & ResponsibilitiesSenior level Clinical Research Specialist with proficiency in BIMO audit preparation needed.
NewSenior Clinical Research Progran Manaager Medtronic PlcSenior Clinical Research Progran ManaagerPlymouth, MNThe following benefits and additional compensation are available to those regular employees who work 20+ hours per week: Health, Dental and vision insurance, Health Savings Account, Healthcare Flexible Spending Account, Life insurance, Long-term disability leave, Dependent daycare spending account, Tuition assistance/reimbursement, and Simple Steps (global well-being program). Utilizes subject matter expertise to provide clinical input to various functions (General Management, Global Strategy & Portfolio Management, Business Development & Licensing, Research & Development, & Marketing) and organizational units to facilitate insightful decision-making and enable achievement of business objectives.
Clinical Research Coordinator II University of MinnesotaClinical Research Coordinator IIMinneapolis, MN$52,000–$63,000 / yearWe are driven to be the choice academic healthcare environment for patients, clinicians, scientists and students who seek exceptional, compassionate, precision cancer therapy; innovative clinical trials and prevention programs; cutting-edge research opportunities; and outstanding advanced education. Located at the heart of one of the nations most vibrant, diverse metropolitan communities, students on the campuses in Minneapolis and St. Paul benefit from extensive partnerships with world-renowned health centers, international corporations, government agencies, and arts, nonprofit, and public service organizations.
Clinical Research Coord III University of MinnesotaClinical Research Coord IIIMinneapolis, MN$65,000–$77,000 / yearWe are driven to be the choice academic healthcare environment for patients, clinicians, scientists and students who seek exceptional, compassionate, precision cancer therapy; innovative clinical trials and prevention programs; cutting-edge research opportunities; and outstanding advanced education. Located at the heart of one of the nations most vibrant, diverse metropolitan communities, students on the campuses in Minneapolis and St. Paul benefit from extensive partnerships with world-renowned health centers, international corporations, government agencies, and arts, nonprofit, and public service organizations.
Clinical Research Coordinator University of MinnesotaClinical Research CoordinatorMinneapolis, MN$32.28–$36 / hourIn addition, the position collaborates with other areas of the University to include Clinical Transitional Science Institute (CTSI) clinical research services, and the staff in the Dermatology clinics, research clinics and research laboratories in assuring that studies meet regulatory requirements, policies and procedures and are completed according to study protocols. Located at the heart of one of the nations most vibrant, diverse metropolitan communities, students on the campuses in Minneapolis and St. Paul benefit from extensive partnerships with world-renowned health centers, international corporations, government agencies, and arts, nonprofit, and public service organizations.
MDR - Sr Prin Clinical Research Spec Artech LLCMDR - Sr Prin Clinical Research SpecMounds View, MN$60–$65 / hourServe as a clinical SME, providing strategic clinical input to leadership and cross-functional teams. Analyze complex clinical data and prepare clear, accurate, and defensible scientific summaries.
Registered Dietitian Clinical Research - PRN Act for HealthRegistered Dietitian Clinical Research - PRNMinneapolis, MinnesotaPerforms the full scope of Registered Dietitian practices; including, but not limited to, providing virtual lifestyle counseling visits to improve nutrition and dietary quality, mental health and developing coping skills, and building health behavior and lifestyle habits that align with participant’s goals and values. Works cooperatively with Clinical Project Manager and site personnel to complete visits and submit accurate source documents in a timely manner.
Sr. Principal Clinical Research Specialist Integrated Resources, IncSr. Principal Clinical Research SpecialistMounds View, MNSummary: Our CER-OMA team supports our clinical-regulatory filings for all pre-market and post-market technologies across all geographies and support our global medical affairs operations with real-time scientific use-case assessments and dissemination. Required Knowledge and Experience: Requires mastery level knowledge of specialty area and working knowledge of several other areas, typically obtained through advanced education combined with experience.
NewClinical Research Assistant Headlands Research IncClinical Research AssistantMaplewood, MN$18–$27 / hourAs a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Join a leading, integrated clinical research network dedicated to high-quality data, patient-centered care, and innovation in clinical trials.
Sr Clinical Research Spec LanceSoft IncSr Clinical Research SpecVirtual, MN$50–$55 / hourResolve operational aspects of clinical trials in conjunction with project teams, adhering to SOPs, GCP, and specific country regulations. Advanced knowledge of clinical trial management systems (CTMS), electronic data capture (EDC), and trial master file (TMF).
Clinical Research Coordinator I Brigham and Women's HospitalClinical Research Coordinator ILexington, MN$21–$29.01 / hourFollowing established policies, procedures, and study protocols, provides assistance on clinical research studies, including recruiting, evaluating, and consenting patients for studies; collecting and organizing patient data; scheduling patients for study visits; performing clinical tests such as phlebotomy, EKGs, etc. and maintaining and updating data generated by the study. The Lurie Center for Autism, a Mass General Brigham program based in Lexington, is a multidisciplinary program designed to evaluate and treat children, adolescents and adults with autism spectrum disorder (ASD) and other neurodevelopmental conditions.
Clinical Research Spec - Exempt LanceSoft IncClinical Research Spec - ExemptVirtual, MN$40–$45 / hourThe majority of time is spent delivering and overseeing the projects from design to implementation while adhering to policies, using specialized knowledge and skills normally acquired through advanced education (typically University). Innovation and Complexity: Problems and issues faced are general and may require understanding of a broader set of issues or other job areas but typically are not complex.
Senior Clinical Research Coordinator Laborie Medical Technologies CorpSenior Clinical Research CoordinatorMinnetonka, MinnesotaWho We’re Looking For: As a key member of the Clinical team, theSenior Clinical Research Coordinator services as an experienced clinical operations professional responsible for independently managing complex clinical research activities across multiple studies. The Senior CRC provides operational leadership for trial master file (TMF) management, payments, and contract administration while driving process improvements, ensuring inspection readiness, and mentoring less experienced team members.
Clinical Research Physician (Principal Investigator/Sub-Investigator) - Full Time Thermo Fisher Scientific IncClinical Research Physician (Principal Investigator/Sub-Investigator) - Full TimeRichfield, MN$240,000–$315,000 / yearDemonstrated ability to collaborate effectively across a matrixed organization, partnering with clinical operations, recruitment, regulatory, pharmacy, laboratory, and sponsor-facing teams to achieve study objectives. As a business of PPD, we are committed to optimizing each step in the patient journey and delivering best-in-class site performance to bring our customers greater certainty to clinical trial delivery.