This individual will apply software Quality Assurance principles in the development, specification, configuration, validation, and implementation of software applications and automated systems per the applicable software lifecycle within the organization. Company Profile Client is a smaller medical device company that’s developed the world’s first fully implanted neurostimulation device for the treatment of obstructive sleep apnea. Primary Responsibilities: Required Qualifications:

The Clinical Research Associate II plays a critical role within the Clinical Affairs department, responsible for site management and/or monitoring activities during clinical trial execution. This position involves working under moderate supervision to ensure compliance with study protocols and regulatory standards. The CRA II plays a pivotal role in maintaining the integrity of clinical data while adapting to the dynamic needs of different studies. Company […]

The Principal Clinical Quality Specialist will support the Clinical Affairs Organization in ensuring the quality and compliance of studies conducted within the clinical portfolio. This role will be responsible for leading and proactively driving clinical quality behaviors, accountability, and cross-functional collaboration (e.g. Clinical Programs, Scientific Affairs, Quality, Regulatory Affairs, Medical Directors, Study Teams, Investigational Trial Sites, and external vendors) with respect to clinical quality assurance […]