Clinical Project Manager Laborie Medical Technologies CorpClinical Project ManagerMinnetonka, MinnesotaChair Clinical Research Team working group and vendor status update meetings and ensure meeting minutes are completed, distributed to team members, and filed in the Trial Master File (TMF) in a timely manner. The CPM , in concert with the Clinical Program Manager, is accountable for achieving successful delivery of Laborie Clinical Team activities at the project level by meeting company and regulatory requirements according to time, quality/scope, and budget constraints.
Senior Clinical Study Manager DanaherSenior Clinical Study ManagerChaska, Minnesota$125,000–$135,000 / yearProvide 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. 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.
Senior Clinical Research Scientist Anteris TechnologiesSenior Clinical Research ScientistEagan, Minnesota$130,000–$160,000 / yearThis position reports to the Senior Manager, Clinical Research and collaborates closely with the broader clinical and cross-functional teams to support ongoing clinical studies, clinical documentation, and the dissemination of clinical data through publications and congress activities. At Anteris Technologies, you’ll join a mission-driven team dedicated to improving the lives of patients with aortic stenosis through breakthrough structural heart technologies while helping shape the future of structural heart care.
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.
NewSenior 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.
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.
Clinical Research Coordinator (DCR) DaVita IncClinical Research Coordinator (DCR)Edina, MN$50,000–$76,000 / yearWe are looking for a highly motivated, positive and innovative Clinical Research Study Coordinator (Research Coordinator) to lead in the coordination, management and conduct of nephrology clinical research trials in dialysis centers and physicians practices. Commitment to and role model of DaVita's values with ability to demonstrate those positively and proactively to patients, teammates, management, physicians, and/or vendors (Village Service Partners) in everyday performance and interactions.
Senior Manager, Clinical Operations ZOLL MedicalSenior Manager, Clinical OperationsMinnetonka, MinnesotaRemote$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. Job Summary This position is responsible for leading a growing team to ensure excellence in the design, development, and execution of clinical trials in collaboration with Clinical Operations and cross-functional partners.
Clinical Research Coordinator Fairview Health ServicesClinical Research CoordinatorSt Paul, Minnesota$29.29–$41.35 / hourResponsible 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. This includes a thorough understanding of the trial criteria for participation, an understanding of the disease under study and our local population, the fit with current research portfolio, and any external resources that may be needed.
NewClinical Manager of ARMHS, CTSS, and Peer Specialists AMHERST H. WILDER FOUNDATIONClinical Manager of ARMHS, CTSS, and Peer SpecialistsSt. Paul, MNFrom life-changing youth interventions (CTSS) and transformative adult recovery (ARMHS) to our invaluable Peer Specialist networks, you will lead the teams making a real, measurable difference every day. A strong candidate will have strong relational skills, demonstrated leadership experience, appreciation for the technical aspects of compliance, and contribute to a culture of positivity and growth.
Sr. Program Manager, Clinical Chemistry & Immunoassay (Business Unit) DanaherSr. Program Manager, Clinical Chemistry & Immunoassay (Business Unit)Chaska, Minnesota$160,000–$175,000 / yearLead, mentor and develop high-performing teams through shared purpose and project goals—leveraging advanced leadership, communication, influence, cross-cultural awareness, negotiation, and conflict resolution skills to consistently meet objectives. Drive high-impact, business-critical programs utilizing Danaher Business System (DBS) tools and methodologies to ensure operational excellence in efficiency, quality, budget, schedule and resource optimization to achieve Quality, Cost, and Delivery (QCD) objectives.
Principal Clinical Scientist (Neurodegenerative) DanaherPrincipal Clinical Scientist (Neurodegenerative)Chaska, Minnesota$120,000–$130,000 / yearThe essential requirements of the job include: Bachelor’s degree in Life Sciences, Healthcare, or a related field with 9+ years of experience in clinical research, specifically with significant experience in US and/or EU trials, or a Master’s degree with 12+ years of experience or Doctoral degree with 4+ years of same experience. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company’s sole discretion, consistent with the law.
Principal Clinical Scientist DanaherPrincipal Clinical ScientistChaska, Minnesota$120,000–$165,000 / yearThe essential requirements of the job include: Bachelor’s degree in Life Sciences, Healthcare, or a related field with 9+ years of experience in clinical research, specifically with significant experience in US and/or EU trials, or a Master’s degree with 12+ years of experience or Doctoral degree with 4+ years of same experience. It would be a plus if you also possess previous experience in: Experience in study designs for diagnostic technologies (IVD) is highly preferred, specifically for Clinical Chemistry, Immunoassays, Hematology, Urinalysis, Flow Cytometry, and/or Biomarkers.
NewPrincipal Project Manager/Clinical Evaluation Reporting (on-site) Abbott LaboratoriesPrincipal Project Manager/Clinical Evaluation Reporting (on-site)St. Paul, MN$114,000–$228,000 / yearThe primary function of a Regulatory Project Manager, Clinical Evaluations ("Clinical Evaluation Report (CER) Project Manager (PM)") is to combine understanding of scientific and research methodology, medical device regulations and guidelines, and product and therapeutic area knowledge to support Regulatory Affairs medical device submissions in the EU for CE Marking of new devices and maintaining of CE Mark for existing devices in accordance with EU MDR 2017/745, MEDDEV 2.7/1 Rev 4, MDCG Guidance documents, and predicate MDD and AIMDD directive requirements. Facilitate communication and exchange of documents between stakeholders (e.g., internal personnel such as Regulatory Affairs, R&D, Clinical R&D, A&P and Marketing, Library Services, Quality Engineering, Clinical Affairs, Risk Management, Program Management, as well as external vendors such as CROs, Medical Writers and Physician Reviewers).
Concordia University St Paul - Clinical Adjunct Faculty - St Paul, MN Orbis Education Services IncConcordia University St Paul - Clinical Adjunct Faculty - St Paul, MNSt. Paul, MNThe Concordia University St. Paul Accelerated BSN program is seeking for highly energetic, Nursing Instructors to oversee student clinical rotations in the Twin Cities area. As a Nursing Clinical Adjunct Instructor and extended faculty member, the primary responsibility is the clinical education of the students in the ABSN program.
Concordia University St Paul - Clinical Adjunct Faculty - Obstetrics/Labor & Delivery Orbis Education Services IncConcordia University St Paul - Clinical Adjunct Faculty - Obstetrics/Labor & DeliverySt. Paul, MNThe Concordia University St. Paul Accelerated BSN program is seeking for highly energetic, Nursing Instructors to oversee student clinical rotations in the Twin Cities area. Our partners leverage our expertise to produce thousands of high-quality graduates ready to enter the workforce and meet employers' demands.
Finance Manager, Clinical FP&A Medica Services Company LLCFinance Manager, Clinical FP&AMinnetonka, MN$88,800–$133,245 / yearPart timeThis role partners closely with clinical leadership, operational teams, and executive stakeholders to ensure financial performance, regulatory compliance, cost management, and informed decision-making across clinical programs and departments. Annual salary range placement will depend on a variety of factors including, but not limited to, education, work experience, applicable certifications and/or licensure, the position's scope and responsibility, internal pay equity and external market salary data.
Program Manager IV - Clinical Optimization Medica Services Company LLCProgram Manager IV - Clinical OptimizationMinnetonka, MN$88,800–$133,245 / yearPart timeAnnual salary range placement will depend on a variety of factors including, but not limited to, education, work experience, applicable certifications and/or licensure, the position's scope and responsibility, internal pay equity and external market salary data. The Program Manager IV is responsible for driving complex, cross-functional programs that impact clinical platforms such as GuidingCare and Wellframe, translating business strategy into executable plans across people, process, and technology.
Part-Time Licensed Clinical Psychologist (PsyD/PhD) - Psychological Testing/Assessment Specialist Associated Clinic of PsychologyPart-Time Licensed Clinical Psychologist (PsyD/PhD) - Psychological Testing/Assessment SpecialistApple Valley, MinnesotaAssociated Clinic of Psychology (ACP) is seeking passionate, skilled, and licensed Clinical Psychologists (PhD or PsyD) to join our growing outpatient team. Work alongside leading clinicians like Dr. John Brose, recipient of the 2020 Minnesota Gerontologist of the Year award and lifetime honoree by the American Psychological Association.