SecondWave is hiring a clinical research associate to support clinical trial efforts and device implementation in multiple cities across the U.S., with the company’s headquarters in Saint Paul, MN acting as the home base for study operations. A key area of focus will be facilitating a clinical study investigating ultrasound stimulation of the spleen to treat rheumatoid arthritis.
SecondWave Systems is developing a noninvasive, wearable ultrasound stimulation device to treat rheumatoid arthritis. This is an emerging modality in medicine that will provide patients and their physicians a new option for treating inflammatory diseases.
SecondWave is hiring a clinical research associate to support clinical trial efforts and device implementation in multiple cities across the U.S., with the company’s headquarters in Saint Paul, MN acting as the home base for study operations. A key area of focus will be facilitating a clinical study investigating ultrasound stimulation of the spleen to treat rheumatoid arthritis.
The individual will perform clinical research investigating splenic ultrasound stimulation in its upcoming clinical study for treating rheumatoid arthritis, but may also support additional studies that run concurrently. Critical to all aspects of this role will be to ensure that research tasks are following the approved protocols and procedures, while maintaining accordance with regulatory requirements.
This role will have considerable patient-facing responsibilities, so professionalism, confidentiality and appropriate bedside manner are essential. A science/research background is preferred, but those with proficient technical skills (familiarity with computers and technology) is sufficient if the candidate has strong patient-facing/medical experience.
75% - Interact and coordinate activities with human participants in studies. This includes interacting with participants through in-person and virtual sessions. The individual will train participants on the use of the investigational ultrasound device and oversee that treatment is administered properly. The individual will learn the protocols and methods that are required for each project, monitor procedures to ensure safety of the staff and participants, collect key study data, manage and support study equipment deployed in the field, and oversee preparation and accurate management of trial documentation. The individual will interact with clinicians and nursing staff at the study sites, and help workflow and interactions between participants and study staff. These activities will involve travel to partner clinical trial sites and to the participant’s homes near those sites throughout the study.
25% - Support clinical trial tasks and company operations with clinical and industry collaborators. Some tasks will involve data entry and management, tabulation of biological/imaging data, and quality control of the research data. The candidate will also assist in preparing reports and presentations, and be involved in meetings and discussions with clinicians, industry partners, and other researchers.
All required qualifications must be included in the application materials
Required Qualifications:
The physical demands and work environment characteristics described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may enable individuals with disabilities to perform the essential functions.
Pay Range: $80,000- $110,000; depending on education/qualifications/experience
FLSA Status: Full Time Exempt
SecondWave Systems offers a comprehensive benefits package that includes:
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EOE/Minorities/Females/Vet/Disability. SecondWave Systems reserves the right to alter, change, modify and/or terminate this job posting at any time without advance notice, or obligation, to any party.
$80,000 - $110,000 per year