Registered Nurse / Clinical Manager, Home Health AccentCare, Inc.Registered Nurse / Clinical Manager, Home HealthBurnsville, MN$110,000–$115,000This includes the coordination and management of patient care, and the supervision and coaching of clinical personnel to ensure that care and services are delivered appropriately. If you meet these qualifications, we would love to meet you: Graduate from an approved school of professional nursing and currently licensed to practice as a registered nurse in the state of agency operation.
NewSenior 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 Research Manager Minneapolis Heart Institute Foundation IncClinical Research ManagerMinneapolis, MN$115,000–$125,000 / yearA minimum of 2 years of supervisory/manager experience leading highly skilled clinical/medical personal which may include hiring, training, coaching, developing and managing performance of individuals or equivalent and proven experience in influencing, support, and coaching others. Allocates work, delegates assignments, and matches skills to the tasks to ensure that work is assigned at the right level to optimize staff talents and effectiveness.
NewClinical 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.
Per Diem Clinical Research Nurse - Home Visits Science 37 IncPer Diem Clinical Research Nurse - Home VisitsMinneapolis, MN$50–$55 / hourWith interest/expertise in Science 37's decentralized model of care delivery, the Mobile Research Nurse will perform delivery of care to participants as well as collaborate with brick and mortar sites, if indicated, for shared clinical trial implementation. Science 37's Nursing Solutions Group brings together expert nurses who share a passion for organizing, planning and implementing mobile clinical nurse services to participants in clinical trials.
Director of Clinical Research Minnesota OncologyDirector of Clinical ResearchSt. Paul, Minnesota$150,000–$190,000 / yearFunctioning at a highly strategic level providing leadership and guidance in the development of new processes to improve efficiency and effectiveness of organizational strategic outcomes for clinical trials resulting in the success of the research program. Specific knowledge of all aspects of clinical research – ability to read, analyze and interpret technical items such as protocols, informed consent documents, and regulatory documents, ability to solve problems and implement solutions.
Per Diem Clinical Research Nurse - Home Visits Science 37Per Diem Clinical Research Nurse - Home VisitsMinneapolis, MN$50–$55 / hourWith interest/expertise in Science 37's decentralized model of care delivery, the Mobile Research Nurse will perform delivery of care to participants as well as collaborate with brick and mortar sites, if indicated, for shared clinical trial implementation. Science 37's Nursing Solutions Group brings together expert nurses who share a passion for organizing, planning and implementing mobile clinical nurse services to participants in clinical trials.
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.
Clinical Research Coordinator-Neonatal Children's MinnesotaClinical Research Coordinator-NeonatalMNPromotion to next higher level, typically Senior Clinical Research Coordinator (SCRC), 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. Baccalaureate in a health-related field and at least four years of clinical research-related experience; or registered nurse with a current license to practice, and at least two years of clinical research experience; or two years of clinical research-related experience and a master''s degree in a related field.
Clinical Research Project Specialist University of MinnesotaClinical Research Project SpecialistMinneapolis, MN$71,000–$85,000 / yearAt the University of Minnesota, we are proud to be recognized by the Star Tribune as a Top Workplace for 2021, as well as by Forbes as Best Employers for Women and one of America's Best Employers (2015, 2018, 2019, 2023), Best Employer for Diversity (2019, 2020), Best Employer for New Grads (2018, 2019), and Best Employer by State (2019, 2022). 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.
Manager, Clinical Research Specialist Training THV AR (Remote US) Edwards Lifesciences CorpManager, Clinical Research Specialist Training THV AR (Remote US)Minneapolis, MNRemote$126,000–$178,000 / yearResponsible for maintaining an audit ready environment for all aspects of regulatory and non-regulatory audits as it relates to training (e.g., conducting training, identifying SMEs, ensuring the collection of required documentation.) Edwards' groundbreaking work in transcatheter aortic heart valve replacement (TAVR) pioneered an innovative, life-changing solution for patients by offering heart valve replacement without the need for open heart surgery.
NewSr. Clinical Research Specialist Integrated Resources, IncSr. Clinical Research SpecialistMinneapolis, MinnesotaContractorstudy start-up documentation preparation)Set-up and maintain accurate progress and study status tracking logsAssist in the preparation of reports, regulatory submissions, publications and presentationsAssist in the preparation of budgets and project plansIdentify and mitigate quality risk and/or issues associated with assigned studies/activitiesMay arrange conference calls, staff meetings, and training events. Clinical Research SpecialistIntegrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms.
NewRegistered 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.
Clinical Research Associate II AtriCureClinical Research Associate IIMinnetonka, OhioThe CRA II will also conduct site visits including Site Qualification Visits, Site Initiation Visits, Interim Monitoring Visits, and Close Out Visits. The CRA II will be responsible for the study start up process for AtriCure’s Clinical Investigational protocols, which includes and is not limited to the following: protocol review, Informed Consent Development, CRF design, EDC testing, preparation of site-specific logs/documentation and investigator study files.
NewClinical 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 Danaher CorpSenior Clinical Study ManagerChaska, MN$125,000–$135,000 / yearIn this role, you will have the opportunity to: Provide strategic oversight into the operational planning and execution of complex programs and individual In Vitro Diagnostics (IVD) clinical studies from concept to close-out, ensuring adherence to protocols, Good Clinical Practice (GCP), and regulatory requirements. The essential requirements of the job include: Bachelor's degree in Life Sciences, Healthcare, or a related field with 8+ years related work experience or Masters with 6+ years of related experience or Doctoral degree with 3+ years of related experience.
Clinical Study Manager (On-Site US) Danaher CorpClinical Study Manager (On-Site US)Chaska, MNThe essential requirements of the job include: Bachelor's degree in Life Sciences, Healthcare, or a related field with 5+ years related work experience or Masters with 3+ years of related experience or Doctoral degree with 0-2 years of related experience. Conduct regular reviews of clinical study data, site monitoring reports, and operational metrics to identify trends, ensure data integrity, and proactively address any performance or quality issues.
NewSenior Clinical Research Associate - Psychiatry - Central U.S. (Remote) Worldwide Clinical Trials Holdings IncSenior Clinical Research Associate - Psychiatry - Central U.S. (Remote)MNRemote$97,000–$193,000 / yearTypically 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.
Senior Clinical Research Associate - CNS/Rare Disease - Central U.S. (Remote) Worldwide Clinical Trials Holdings IncSenior Clinical Research Associate - CNS/Rare Disease - Central U.S. (Remote)MNRemote$97,000–$193,000 / yearTypically 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.
Clinical Trial Manager Heartflow IncClinical Trial ManagerMinneapolis, MNRemote$95,000–$125,000 / yearHeartflow is the first AI-driven non-invasive integrated heart care solution across the CCTA pathway that helps clinicians identify stenoses in the coronary arteries (RoadMapAnalysis), assess coronary blood flow (FFRCT Analysis), and characterize and quantify coronary atherosclerosis (Plaque Analysis). The flagship product-an AI-driven, non-invasive cardiac test supported by the ACC/AHA Chest Pain Guidelines called the Heartflow FFRCT Analysis-provides a color-coded, 3D model of a patient's coronary arteries indicating the impact blockages have on blood flow to the heart.
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.
Clinical Research Project Coordinator V MedtronicClinical Research Project Coordinator VMounds View, MinnesotaIf 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).
Clinical Research Coordinator 3 University of MinnesotaClinical Research Coordinator 3Minneapolis, 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 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 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 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.
Sr Clinical Research Specialist Integrated Resources, IncSr Clinical Research SpecialistVirtual, MNRemoteThe majority of time is spent delivering and overseeing the projects from design to implementation while and adhering to policies, using specialized knowledge and skills normally acquired through advanced education (typically University). Conducts registered and nonregistered clinical studies of products that have been determined to satisfy a medical need and/or offer a commercial potential.
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.
Sr Clinical Research Spec Artech LLCSr Clinical Research SpecVirtual, MN$45–$50 / hourSupport protocol development, CRFs, study budgets, and clinical operations. Excellent communication, organization, and project management skills.
Senior Clinical Research Associate - CNS - Central U.S. (Remote) Worldwide Clinical Trials Holdings IncSenior Clinical Research Associate - CNS - Central U.S. (Remote)MNRemote$97,000–$193,000 / yearTypically 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.
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.
Research Professional 2 - Lillehei Clinical Research Unit/Cardiovascular University of MinnesotaResearch Professional 2 - Lillehei Clinical Research Unit/CardiovascularMinneapolis, MN$55,000–$70,000 / yearCommunicate information about assigned studies to other University faculty/staff, including details of study, inclusion/exclusion criteria, other enrollment requirements, visit needs, etc., leading training of study staff, clinical, and lab partners on study protocols activities as it relates to their roles on the study. 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.
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).
NewSenior Clinical Trial Associate Sarepta Therapeutics IncSenior Clinical Trial AssociateMN$107,200–$134,000 / yearThe salary offer is commensurate with Sarepta's compensation philosophy and considers factors including, but not limited to, education, training, experience, external market conditions, criticality of role, and internal equity. Coordinates and tracks the distribution and subsequent retrieval of clinical documents, including but not limited to protocols, protocol amendments, IBs, ICF's, monitoring visit reports, etc.
Senior Clinical Research Associate AtriCureSenior Clinical Research AssociateMinnetonka, OhioCRA) at AtriCure plays a vital role in the Clinical Affairs department, independently managing and overseeing site management and/or monitoring activities during clinical trial execution. Liaise with clinical study management, field personnel, and CROs, addressing moderately complex protocol or study related issues as necessary.
NewAssociate Clinical Data Manager AbbottAssociate Clinical Data ManagerMaple Grove, Minnesota$78,000–$156,000 / yearConducts complex 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. As the customer-face oftheData Reviewteamand its primary liaison with theClinicalprojectteam, theAssociateClinical Data Manager’s in-depthclinical operations andtherapy-specific knowledge ensures alignment to customerneeds, andinforms review and analysis of study data.
Clinical Research Coordinator Fairview Health Services IncClinical Research CoordinatorSt Paul, MNFairview offers a generous benefit package including but not limited to medical, dental, vision plans, life insurance, short-term and long-term disability insurance, PTO and Sick and Safe Time, tuition reimbursement, retirement, early access to earned wages, and more! Responsible for interpretation, application of and compliance with Federal Regulations, Good Clinical Practice, and University and Clinical Partner policies as it relates to assigned protocols as well as application of subject matter knowledge.
Manager, Global Clinical Trial Operations Boston Scientific CorpManager, Global Clinical Trial OperationsArden Hills, MNThe Manager, Global Clinical Trial Operations provides leadership to assigned trial operations team members in support of global, cross-divisional clinical trials and related objectives for new products, product enhancements and process changes. The anticipated compensation listed above and the value of core and optional employee benefits offered by Boston Scientific (BSC) - see www.bscbenefitsconnect.com-will vary based on actual location of the position and other pertinent factors considered in determining actual compensation for the role.
Clinical Research Coordinator I/Ii/Iii Opportunities - Multiple Locations Nationwide Headlands ResearchClinical Research Coordinator I/Ii/Iii Opportunities - Multiple Locations NationwideMaplewood, MN$45,000–$100,000 / yearThis 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.
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.
Provider Clinical Operations Consultant, Senior Manager PricewaterhouseCoopers LLPProvider Clinical Operations Consultant, Senior ManagerMinneapolis, MN$124,000–$280,000 / yearPreference for at least one of the following fields of study: Accounting, Actuarial Science, Analytics/Data Science, Business Administration/Management, Computer Science/Information Systems, Economics, Engineering, Finance, Government/Public Policy, Health Administration/Public Health, Mathematics/Statistics, Operations/Supply Chain, Organizational Management/Behavior, Risk Management/Insurance. 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 .
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.
Senior Manager, Clinical Operations Zoll Medical CorpSenior Manager, Clinical OperationsMinnetonka, MNRemote$150,000–$175,000 / yearLead and manage clinical trial operational execution, including site and principal investigator identification, subject recruitment, investigator meetings, monitoring, trial master files maintenance and resolution of site performance issues. The Respicardia division of ZOLL Medical Corporation is focused on helping people with central sleep apnea get access to a therapy to restore a more normal breathing pattern during sleep and give them better quality of life.
Prin Clinical Research Spec Medtronic PlcPrin Clinical Research SpecMounds View, 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.
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.
Clinical Research Engagement Lead (CREL) - Central Region (St. Paul/Minneapolis, MN) Genentech IncClinical Research Engagement Lead (CREL) - Central Region (St. Paul/Minneapolis, MN)MN$108,000–$202,000 / yearRelationship 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).
NewClinical Data Coordinator Integrated Resources, IncClinical Data CoordinatorMounds View, MinnesotaFull timeOracle Clinical) and report toolsAble to perform routine data management tasks with minimal supervision; receives instruction on new projectsAbility to use judgment to effectively solve problemsEffective oral and written communication skillsAbility to prioritize tasks and manage competing priorities based on project plan expectationsTeam player who effectively works with colleaguesExperience using Microsoft Office productsHigh degree of initiative and self-motivation with a strong sense of accountabilityLocal candidate to Minneapolis, MN required Good understanding of concepts of data management activities (CRF/Edit check development, data management plans, snapshots, data review, and data quality).Ability to identify data related issues using study database and data management reports and escalate issues appropriately.
NewClinical Customer Representative Integrated Resources, IncClinical Customer RepresentativeChanhassen, MinnesotaContractorClinical Assistant reports directly to the PASS Administrative Supervisor.• Data entry of patient information in dedicated software• Reporting patient enrollment status to supervising Nurse Specialist• Updating patient records• Maintaining spreadsheets• Sending out program overview mailers to new enrollees• Faxing as directed• Other projects as required and assigned by the PASS Administrative SupervisorEDUCATION REQUIRED: High school diplomaYEARS OF EXPERIENCE: Minimum one-year customer service or HUC related experiencePHYSICAL JOB REQUIREMENTS: Physical capabilities to perform the job. Clinical Customer RepresentativeIntegrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms.
Associate Clinical Data Manager Abbott LaboratoriesAssociate Clinical Data ManagerMaple Grove, MN$78,000–$156,000 / yearConducts complex 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 data review, 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.