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).
Sr 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.
Travel Clinical Research Coordinator Thermo Fisher ScientificTravel Clinical Research CoordinatorRichfield, MinnesotaJoin us as a Travelling Clinical Research Coordinator – To oversee and manage clinical operations at our research site, ensuring compliance with study protocols and regulatory guidelines, providing training and support to staff, and serving as a liaison between the site and clinical trial sponsors to facilitate successful study execution and patient enrollment. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services.
Clinical Research Coordinator Thermo Fisher ScientificClinical Research CoordinatorRichfield, MinnesotaJoin us as a Clinical Research Coordinator I – To coordinate and manage clinical trials, ensuring adherence to protocols, regulatory requirements, and timelines while working closely with the clinical team to support patient recruitment, data collection, and documentation efforts for advancing medical research. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services.
NewClinical Research Associate (CRA II/Senior) - Oncology - US Any Region Parexel International CorpClinical Research Associate (CRA II/Senior) - Oncology - US Any RegionMNWith 22,000+ employees worldwide, we partner with biopharmaceutical companies and research sites to design and deliver patient-focused clinical trials that broaden access and make research a care option for anyone, anywhere. As a CRA, you will manage clinical sites from identification through closeout, serving as the primary point of contact for site teams and helping ensure study quality, patient safety, regulatory compliance, and accurate clinical data.
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.
Senior 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/Psychiatry - Central U.S. Worldwide Clinical Trials Holdings IncSenior Clinical Research Associate - CNS/Psychiatry - Central U.S.MN$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 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 .
Senior Clinical Research Specialist - NV - Irvine, CA; Lafayette, CO or Fridley, MN (Onsite) Medtronic PlcSenior Clinical Research Specialist - NV - Irvine, CA; Lafayette, CO or Fridley, MN (Onsite)Fridley, 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).
Senior Clinical Research Specialist - NV - Irvine, CA; Lafayette, CO or Fridley, MN (Onsite) MedtronicSenior Clinical Research Specialist - NV - Irvine, CA; Lafayette, CO or Fridley, MN (Onsite)Fridley, 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 Nurse - Maple Grove / Coon Rapids Minnesota OncologyClinical Research Nurse - Maple Grove / Coon RapidsMaple Grove, Minnesota$90,000–$125,000 / yearDuties include assuring protocol compliance for all patients on trial, participation in consent process, ongoing assessments for changes in condition and adverse events, accurate and timely documentation/data entry, responsible for education and training of other staff and patients, understands the strategic and operational objectives of the research program, may performs high level financial work including budget oversight. Working independently, reviews patients for changes in condition, adverse events, concomitant medication use, protocol compliance, response to study drug and thoroughly documents and reports all findings to physician and care team.
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.
Experienced Clinical Research Associate (CRA II/Sr CRA) - US Central - Multiple Therapeutic Areas Available Thermo Fisher Scientific IncExperienced Clinical Research Associate (CRA II/Sr CRA) - US Central - Multiple Therapeutic Areas AvailableMN$66,800–$125,000 / yearWhat You'll Do: 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.
Clinical Research Program Manager (MCRS Strategic Account Manager) MedtronicClinical Research Program Manager (MCRS Strategic Account Manager)Minneapolis, MinnesotaRemoteThe 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 Manager II Minneapolis Heart Institute Foundation IncClinical Research Manager IIMinneapolis, MN$125,000–$135,000 / yearThe CRM II leads enterprise-wide initiatives, drives cross-functional collaboration and integration, mentors research staff and other Clinical Research Managers, and may oversee shared services or multiple enterprise-level functions. As a Clinical Research Manager II (CRM II), you will do more than oversee research operations-you will provide strategic leadership, build high-performing teams, and strengthen the partnerships and programs that help change and save lives.
Clinical Research Associate II Inspire therapyClinical Research Associate IIMinneapolis, Minnesota$95,000–$125,000 / yearApplicants 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 Inspire Medical Systems participates in E-Verify. Perform 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.
Clinical Research Associate II Inspire Medical Systems Inc.Clinical Research Associate IIMinneapolis, MN$95,000–$125,000 / 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 .
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.
Sr. Field Clinical Research Specialist MedtronicSr. Field Clinical Research SpecialistMinneapolis, MinnesotaMust possess at least two (2) years’ experience with each of the following: GCP and regulatory compliance guidelines for clinical trials including Clinical Trial Design and Execution (Phase I-IV); Clinical study Start-up, site initiation, monitoring, and close-out; Review and development of ICF, Protocol, and amendments; Patient recruitment and retention strategies, SDV, AE and SAE reporting; FDA Regulations 21 CFR Parts 11, 50, 54, 56, 312, 812, and ICH-GCP (E6 R2/R3) Compliance; IRB/IEC Submission and approval process; CAPA development and implementation, and HIPAA compliance; and CTMS, Veeva Vault CTMS, Oracle Siebel CTMS, and Salesforce. 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).