Clinical Research Associate-Cancer and Blood Disorders Children's MinnesotaClinical Research Associate-Cancer and Blood DisordersMNPromotion to next higher level, typically CRA II, is determined by the Clinical Research Program Manager through performance reviews that take into account both experience carrying out the department''s job-related duties/tasks, as well as a demonstrated commitment to professionalism in carrying out those tasks in line with Children''s values and organizational policies and procedures. The department at Children's of Minnesota provides care for children of all ages with all types of malignancies including brain tumors, solid tumors, and leukemia; and blood disorders such as sickle cell disease, bleeding disorders, and anemia.
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.
Senior Clinical Study Manager Inspire therapySenior Clinical Study ManagerMinneapolis, MinnesotaManage study safety by tracking and reporting adverse events as required by regulatory bodies, reviewing adverse event trends, and overseeing safety committees including Clinical Events Committees and Data Safety Monitoring Boards. Oversee monitoring activities related to assigned clinical studies including review and approval of monitoring plan and monitoring reports, managing monitoring schedule and ensuring corrective action related to monitoring findings.
Senior Clinical Study Manager Inspire Medical Systems Inc.Senior Clinical Study ManagerMinneapolis, MN$106,000–$170,000 / yearManage study safety by tracking and reporting adverse events as required by regulatory bodies, reviewing adverse event trends, and overseeing safety committees including Clinical Events Committees and Data Safety Monitoring Boards. Oversee monitoring activities related to assigned clinical studies including review and approval of monitoring plan and monitoring reports, managing monitoring schedule and ensuring corrective action related to monitoring findings.
Clinical Research Associate (CRA) II - hybrid in Minneapolis CVRx IncClinical Research Associate (CRA) II - hybrid in MinneapolisBrooklyn Park, MNWe offer a culture of teamwork, collaboration, and positivity, where challenging the status quo is welcomed, continuous learning is valued, and each of us has an opportunity to make a significant impact in an exciting, purpose-driven startup environment while also having fun. The Clinical Research Associate (CRA) II performs the day-to-day operations associated with the execution of clinical trials and is responsible for the direct contact with assigned clinical investigative sites.
NewSr Clinical Research Spec Medtronic PlcSr Clinical Research SpecMounds View, MNIf you are applying to perform work for Medtronic, Inc. ("Medtronic") in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can find here a list of all material job duties of the specific job position which Medtronic reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment. The 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).
NewPSG Tech and Clinical Research Coordinator University of MinnesotaPSG Tech and Clinical Research CoordinatorMinneapolis, MN$31.73–$38.47 / 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. Main duties include setting up home based sleep studies, education of participants in sleep equipment and troubleshooting equipment issues with participants, analyzing data, and ensuring all data handling complies with privacy rules.
Clinical Quality Manager Medtronic PlcClinical Quality ManagerMounds View, MNIf you are applying to perform work for Medtronic, Inc. ("Medtronic") in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can find here a list of all material job duties of the specific job position which Medtronic reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment. The 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).
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.
NewAssociate Clinical Data Manager # 26-19584 US Tech Solutions, Inc.Associate Clinical Data Manager # 26-19584Maple Grove, MNConducts review and analysis of subject data as it accumulates, resolving discrepant or aberrant data points via individual queries to study sites, as well as the identification of systemic and/or significant data quality issues requiring escalation; manages escalation efforts and drives them to resolution in partnership with Project Management, Site Management, Clinical Science, Biometrics, Safety, and organizational leaders. Leads proactive partnership, on both an ad hoc and period/prescribed basic, with field and study team personnel, presenting findings and issues uncovered during central monitoring and data review activities, devising and documenting appropriate resolution and escalation strategies, and managing the overall health of data quality and study conduct through milestones and deliverables over the lifecycle of the study.
Sr Clinical Research Spec LancesoftSr Clinical Research SpecVirtual, MN$50Resolve 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 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.
NewSr Clinical Research Spec Artech LLCSr Clinical Research SpecMinneapolis, MN$50–$55 / hourExperience coordinating clinical studies with cross-functional teams, sites, vendors, and investigators . Experience working for an industry sponsor ; medical device experience strongly preferred .
Sr. Clinical Research Director (CRDN) Medtronic PlcSr. Clinical Research Director (CRDN)Minneapolis, 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). If you are applying to perform work for Medtronic, Inc. ("Medtronic") in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can find here a list of all material job duties of the specific job position which Medtronic reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment.
NewSr Clinical Research Spec - Exempt LanceSoft IncSr Clinical Research Spec - ExemptMinneapolis, MN$50–$55 / hourRequires a University Degree and a minimum of 4 years of relevant experience, or an advanced degree with a minimum of 2 years of relevant experience. Conduct registered and nonregistered clinical studies of products that satisfy medical needs or offer commercial potential.
Clinical 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.
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.
Head of Clinical and Medical Affairs Saluda Medical Pty LtdHead of Clinical and Medical AffairsMinnetonka, MNKnowledge/Skills/Abilities: Knowledge of neuroscience and/or biomedical science Excellent verbal and written communication Ability to think creatively, dynamically, and foster a culture of commitment to thoughtful science to help patients in need Demonstrated leadership experience, including excellent strategic, analytical, planning, and communication skills in a dynamic, fast-paced environment Leadership style that demonstrates professionalism, encourages accountability, and establishes an environment of mutual respect Maturity, confidence and credibility to advise and influence senior management Excellent organizational and project management skills with a high degree of attention to detail High degree of personal integrity. What Youll Bring: 15+ years direct clinical and/or medical affairs experience in medical devices including experience with Active Implantable Medical Devices A minimum of a Masters degree in science/biomedical/health related field; PhD preferred Experience with neurostimulation industry preferred Active implantable experience in neuromodulation field preferred Demonstrated success in working with FDA and/or other regulatory and governmental agencies Demonstrated success in developing clinical evidence strategies, and designing and conducting clinical trials in support of medical device and/or pharmaceuticals.
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.