Current jobs related to Clinical Research Monitor, Midwest - Madison - Edwards Lifesciences


  • Madison, Wisconsin, United States CRU Fortrea Clinical Research Unit Inc. Full time

    Job SummaryCRU Fortrea Clinical Research Unit Inc. is seeking a highly motivated and detail-oriented Research Technician to join our team. As a Research Technician, you will play a critical role in the success of our clinical trials by providing high-quality care to participants and ensuring the smooth operation of our research units.Key...


  • Madison, United States CRU Fortrea Clinical Research Unit Inc. Full time

    As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...


  • Madison, Wisconsin, United States Midwest Clinical Resource in Southeast Wisconsin Full time

    Join Our Team as a Licensed Practical NurseWe are seeking a skilled and compassionate Licensed Practical Nurse to join our team at Midwest Clinical Resource in Southeast Wisconsin.About the Role:Evaluate patient needs and perform assessments to develop effective care plansAdminister medications and treatments as prescribed by physiciansProvide direct...


  • Madison, Wisconsin, United States Innova Solutions Full time

    Position Overview:Innova Solutions is seeking a dedicated Clinical Trial Assistant I/Research Assistant I to support our clinical research initiatives. This is a full-time contract role with the potential for contract-to-hire opportunities.Key Responsibilities:As a Clinical Trial Assistant I, you will be responsible for:Conducting vital sign assessments...


  • Madison, Wisconsin, United States Midwest Clinical Resource in Southeast Wisconsin Full time

    Join Our Team as a Licensed Practical NurseWe are seeking a skilled and compassionate Licensed Practical Nurse to join our team at Midwest Clinical Resource in Southeast Wisconsin.About the Role:As a Licensed Practical Nurse, you will be responsible for providing high-quality patient care in a long-term care setting. Your duties will include evaluating...


  • Madison, Wisconsin, United States Innova Solutions Full time

    Position Overview:Innova Solutions is seeking a dedicated Clinical Trial Assistant I/Research Assistant I to join our dynamic team. This is a full-time contract position with potential for contract-to-hire opportunities.Key Responsibilities:As a Clinical Trial Assistant I, you will be responsible for a variety of tasks including:Conducting vital sign...

  • MRI Physicist

    2 weeks ago


    Madison, Wisconsin, United States University of Wisconsin Full time

    Job Summary:The Department of Radiology at the University of Wisconsin is seeking a highly skilled Magnetic Resonance Imaging (MRI) Physicist to join our team. This physicist will be responsible for providing technical support for MRI imaging, with a focus on functional MR (fMR) imaging, and will work closely with our team to ensure the safe and effective...


  • Madison, Wisconsin, United States University of Wisconsin Full time

    Job Summary:The Department of Radiology at the University of Wisconsin is seeking a highly skilled Magnetic Resonance Imaging (MRI) Physicist to join our team. This physicist will be responsible for providing technical support for MRI imaging, with a focus on functional MR (fMR) imaging, and will work closely with our team to ensure the safe and effective...


  • Madison, Wisconsin, United States Innova Solutions Full time

    Position Overview:Innova Solutions is seeking a dedicated Clinical Trial Assistant I/Research Assistant I to join our team. This is a full-time contract role with the potential for conversion to a permanent position.Job Details:Location: Madison, WIContract Duration: 3+ monthsWork Schedule: Rotating shifts including AM, PM, and overnight optionsKey...


  • Madison, Wisconsin, United States Mindlance Full time

    Job Title: Clinical Research NurseDuration: Initial assignment of 6 months with potential for full-time employmentShift: Second shift from 3 PM to 11 PM with rotating weekends or varying shifts including 5:30 AM to 1 PM, 6:30 AM to 3 PM, 3 PM to 11 PM, and 11 PM to 7 AM. A new schedule will be provided every Friday for the upcoming two...


  • Madison, Wisconsin, United States University of Wisconsin Full time

    Position Overview:The Department of Medicine is engaged in federally funded NIH or industry-sponsored clinical research involving pharmaceuticals, medical devices, biological agents, imaging technologies, and innovative advancements. This role is pivotal in orchestrating clinical trials within the department, delivering nursing care to research participants,...


  • Madison, Wisconsin, United States University of Wisconsin Full time

    Position Overview:The Department of Medicine is engaged in federally funded NIH or industry-sponsored clinical research that involves pharmaceuticals, medical devices, biologic agents, imaging technologies, and innovative advancements. This role is crucial for coordinating clinical trials within the department, delivering nursing care to research...


  • Madison, Wisconsin, United States University of Wisconsin Full time

    Position Overview:The Department of Medicine is engaged in federally funded NIH or industry-sponsored clinical research that encompasses pharmaceuticals, medical devices, biological agents, imaging, and innovative technologies. This role is pivotal in coordinating clinical trials within the department, delivering nursing care to research participants, and...


  • Madison, Wisconsin, United States University of Wisconsin Full time

    Position Overview:The Department of Radiology within the School of Medicine & Public Health is looking for a Clinical Research Nurse to contribute to innovative medical imaging and disease-oriented initiatives. The Clinical Research Nurse collaborates with a multidisciplinary team, including physicians, PhD researchers, imaging personnel, and other research...


  • Madison, United States FORTREA INC. Full time

    JOB REQUIREMENTS: As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With...


  • Madison, United States FORTREA INC. Full time

    JOB REQUIREMENTS: As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With...


  • Madison, Mississippi, United States Medix™ Full time

    Job Overview:We are seeking a highly skilled Clinical Research Coordinator to join our team at Medix™ to assist in the management and oversight of clinical trials and research studies. The role involves collaborating with the research team to ensure the study runs smoothly and adheres to all protocols and regulations.Key Responsibilities:Study Management:...


  • Madison, Wisconsin, United States Food Management Search Full time

    Position Overview:This is a contract role with potential for permanent placement.Job Title:Clinical Research Nurse - RN or LPNLocation:Madison, WISchedule:Flexible shifts availableJob Code:CVDJPOpportunities:Multiple openings availableBenefits:Comprehensive benefits package offeredJob Description:This position is situated within a clinical research...


  • Madison, Wisconsin, United States University of Wisconsin Full time

    Position Overview:The Division of Hematology, Medical Oncology, and Palliative Care is in search of an academic clinician specializing in Health Services research. We are particularly interested in candidates with expertise in sub-specialties such as Central Nervous System, genitourinary or gastrointestinal tumors, or sarcomas. The selected physician will be...


  • Madison, United States PAREXEL Full time

    Working with heart At the end of the day we’re all patients. Because of this, the Parexel team takes our work personally and does it with empathy and heart. When our values align, there’s no limit to what we can achieve. Our clinical operating model drives effectiveness, reduces handoffs and increases employee, client and site satisfaction. As a...

Clinical Research Monitor, Midwest

4 months ago


Madison, United States Edwards Lifesciences Full time

Imagine how your ideas and expertise can change a patient’s life. We generate extensive clinical evidence to demonstrate the effectiveness and safety of our innovations and how our products transform patients’ lives. As part of our Clinical Affairs team, you’ll hone your scientific curiosity and passion for evaluating data to increase access to pioneering technologies for patients in need. In close partnership with principal investigators, dedicated medical professionals, patient advocacy groups, and regulatory authorities, you will drive the evidence needed to optimize patient outcomes. Aortic stenosis impacts millions of people globally, yet it often remains under-diagnosed and undertreated. 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. Our Transcatheter Heart Valve (THV) business unit continues to partner with cardiologists and clinical teams to transform patient care with devices supported by clinical evidence. It’s our driving force to help patients live longer and healthier lives. Join us and be part of our inspiring journey. As the Clinical Research Monitor on the Aortic team, you will ensure trial patients' safety by assuring trials are conducted ethically and within regulatory compliance, data accuracy, and protocol adherence. How you'll make an impact: Field monitor of studies and data collection for clinical trials, assess all data documentation, reports, records, transcripts, exam results for consistency with case report form, and determine if clinical trial/study subject documentation is within parameters of study hypothesis, as well as to monitor clinical trial/study safety, in keeping with protocols, GCP (Good Clinical Practices) and regulatory requirements. Provide oversight of and insights into trial activities (e.g., trends in protocol compliance, enrollment, monitoring deviations, data quality) to principal investigators and support staff, and study sponsor management and leadership staff, including Institutional Review Boards/Ethics Committees/Research Ethics Committees, Clinical Operations (e.g. Contracts), and recommend and develop process improvements. Verify trial/study data, including maintaining appropriate regulatory documents both internal and external, auditing to be sure the site has the appropriate regulatory documentation to conduct the trial/study, and source documentation is properly recorded. Validate investigational device accountability by tracking the history of investigational devices from Edwards to the field sites and through final disposition. Develop and deliver training on GCPs, protocols, database, compliance, device accountability, adverse event reporting, study investigation protocols, amendments, regulatory documentation requirements as well as training and proctoring new employees on trial and study related activities. Contribute to the development of clinical protocols, informed consent forms, and case report forms. Edit/amend informed consent documents. Other incidental duties What you'll need (Required): Bachelor's Degree or Equivalent in Life Sciences or Nursing 3 years experience in clinical research (as a CRC or CRA) including quality assurance/control and regulatory compliance or field monitoring Experience working in a medical device or regulated industry Experience with electronic data capture Ability to travel up to 75% for clinical site visits Covid Vaccination What else we look for (Preferred): Strong written and verbal communication skills, presentation skills, interpersonal relationship skills, and analytical skills are required Proven expertise in MS Office Suite and clinical systems, including Word, Excel, Adobe, and ability to operate general computer software and office machinery Demonstrated problem-solving and critical thinking skills Strong understanding of cardiovascular anatomy, pathology and physiology or Business Unit area of expertise Substantial understanding of medical device regulatory requirements and documents, device accountability and adverse events reporting Technical writing skills (protocols, CRF development, study tools) Ability to communicate and relate well with key opinion leaders and clinical personnel Adhere to all company rules and requirements (e.g., pandemic protocols, Environmental Health & Safety rules) and take adequate control measures in preventing injuries to themselves and others as well as to the protection of environment and prevention of pollution under their span of influence/control Edwards is an Equal Opportunity/Affirmative Action employer including protected Veterans and individuals with disabilities. COVID Vaccination Requirement Edwards is committed to complying with the requirements and guidance from our government authorities and to protecting our vulnerable patients and the healthcare providers who are treating them around the world. As such, all Healthcare Interacting positions require COVID-19 vaccination, which includes anyone who directly interfaces with patients and those who interact with healthcare providers as part of their role. If hired, as a condition of employment, you will be required to submit proof that you have been fully vaccinated for COVID-19, unless you request and are granted a medical or religious accommodation for exemption from the vaccination requirement. This vaccination requirement does not apply in countries where it is prohibited by law to impose vaccination. In countries where vaccines are less available, or other requirements exist, we may institute alternate measures that optimize patient safety and healthcare provider safety, which may include regular COVID testing or specific masking requirements. Edwards Lifesciences is the global leader in patient-focused medical innovations for structural heart disease, as well as critical care and surgical monitoring. Driven by a passion to help patients, the company collaborates with the world's leading clinicians and researchers to address unmet healthcare needs, working to improve patient outcomes and enhance lives. Headquartered in Irvine, California, Edwards Lifesciences has extensive operations in North America, Europe, Japan, Latin America and Asia and currently employs over 15,000 individuals worldwide. For us, helping patients is not a slogan - it's our life's work. From developing devices that replace or repair a diseased heart valve to creating new technologies that monitor vital signs in the critical care setting, we focus on helping patients regain and improve the quality of their life.