Sonova Group · 20 hours ago
Clinical Research Specialist
Sonova Group is a company focused on hearing technologies, and they are seeking a Clinical Research Specialist to collaborate with research partners on post market clinical studies. The role involves designing and implementing clinical studies, establishing relationships with clinicians, and ensuring compliance with regulatory standards.
Medical Device
Responsibilities
Design and implementation of clinical studies on AB products consistent with Global Clinical Research strategies to confirm safety/efficacy and investigate particular features of AB technology
Establish relationships with clinicians on a scientific level and communicate results internally and externally
Execution of clinical studies, including: contracts, insurance, ethical approvals, competent authority approvals (if applicable to study), study documentation, clinical staff training, site initiation on-site monitoring, complete and timely review of site and clinical trial data, appropriate data reporting, study close-out visits, coordination/support of study results for publications, abstracts, poster presentations at scientific conferences
Development of a high level of professional scientific, technical, clinical and regulatory clinical expertise through familiarity with relevant literature by attending scientific meetings, and by interacting with various experts or institutions
Training of investigators, clinic staff and AB field staff, where required
Qualification
Required
Master's degree (or equivalent) in Audiology and a minimum of 5 years of experience in cochlear implants or a closely related industry
Strong knowledge of medical terminology, clinical study design, regulatory compliance for clinical research trials, and statistical techniques for data analysis
Results-driven self-starter with strong problem-solving skills, attention to detail, and the ability to manage multiple tasks and priorities in a fast-paced environment
Demonstrated credibility and professionalism, with the ability to collaborate effectively across cross-functional and remote teams and communicate clearly with internal and external stakeholders
Proficiency in English and Microsoft Office
A minimum of 200Mb/sec download and 10Mb/sec upload speed internet connectivity is required to support any remote/hybrid employee functionality at Sonova
Preferred
Doctorate in Audiology and experience in regulatory clinical research
Expertise in cochlear implant and/or hearing aid signal processing, clinical fitting concepts, and experience in regulated medical or laboratory environments
Proficiency in German and/or Spanish and experience using statistical software
Benefits
Medical, dental and vision coverage
Health Savings, Health Reimbursement, Flexible Spending/Dependent Care Accounts
TeleHealth options
401k plan with company match
Company paid life/ad&d insurance
Company paid Short/Long-Term Disability coverage (STD/LTD)
Accident/Hospital Indemnity coverage
Legal/ID Theft Assistance
PTO (or sick and vacation time), floating Diversity Day, & paid holidays
Paid parental bonding leave
Employee Assistance Program (24/7 mental health support hotline, 5 company paid counseling sessions and more)
Robust Internal Career Growth opportunities
Tuition reimbursement
Hearing aid discount for employees and family
Internal social recognition platform
Plan rules/offerings dependent upon group Company/location.
Company
Sonova Group
Around 25% of the world’s population is living with hearing loss.
H1B Sponsorship
Sonova Group has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (1)
2024 (3)
2023 (1)
2022 (3)
2020 (1)
Funding
Current Stage
Late StageLeadership Team
Recent News
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2024-04-07
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