Principal Scientist | REMOTE

Sonova USA, Inc.; California; Hybrid; USD 114,000 - 143,000; Full time

Benefits offered by this job

Medical coverage

Dental coverage

Vision coverage

401k with company match

Life insurance

Disability coverage

Paid time off

Parental leave

Tuition reimbursement

Hearing aid discount

Job summary

Sonova USA, Inc. is seeking a Principal, Clinical Scientist to provide scientific leadership across global clinical development programs for innovative medical device technologies.

You will design studies, support regulatory submissions, generate evidence, and communicate findings across the product lifecycle. The role requires a Master's degree (Life Sciences or related), 8+ years in clinical development or Medical Affairs, and strong scientific writing and regulatory knowledge.

Qualifications

• Master's degree in Life Sciences, Health Sciences, or related field.
• Eight+ years in clinical development, clinical research, Medical Affairs, or Scientific Affairs, including protocol development.
• Experience producing Clinical Study Reports and regulatory documents.

Responsibilities

• Lead scientific design and oversight of pivotal, post-market, and real-world studies from concept to publication.
• Develop protocols, CSRs, literature reviews, and other regulatory documents.
• Support regulatory submissions with scientific justifications and health-authority interactions.
• Analyze and interpret clinical evidence to guide development and lifecycle management.
• Collaborate with Regulatory, QA, R&D, and external experts to advance programs.
• Lead development and review of manuscripts, abstracts, posters, and publications.
• Support publication strategies and scientific training for conferences.

Skills

ICH-GCP knowledge

FDA regulations

Scientific writing

Analytical thinking

Cross-functional collaboration

Project management

Public speaking

Education

Master's degree in Life Sciences or related

PhD or AuD (preferred)

Job description

Who we are

At Sonova, we envision a world where everyone can enjoy the delight of hearing. This vision inspires us and fuels our commitment to developing innovative solutions that improve hearing health and human connection - from personal audio devices and wireless communication systems to hearing aids and cochlear implants. We're dedicated to providing outstanding customer experiences through our global audiological care services, ensuring that everyone has the opportunity to engage fully with the world around them.

Guided by a culture of continuous improvement that fosters resilience and self-motivation, our team is united by a shared commitment to excellence and a deep sense of pride in our work, each of us playing a vital role in creating meaningful change,

Here you'll find a diverse range of opportunities that span both consumer and medical solutions and the freedom to shape your career while making an impact on the lives of others. Join us in our mission to create a more connected world, where every voice is heard and every story matters.

Valencia, California - Hybrid preferred | REMOTE FOR THE RIGHT CANDIDATE

Principal Scientist | REMOTE

Principal, Clinical Scientist

Join Advanced Bionics as a Principal, Clinical Scientist and provide scientific leadership across global clinical development programs supporting innovative medical device technologies. In this highly collaborative role, you will lead clinical study design, regulatory scientific strategy, evidence generation, and scientific communication across the product lifecycle to support regulatory approvals, indication expansions, and Medical Affairs initiatives.

Responsibilities

• Lead the scientific design, development, and oversight of pivotal, post-market, investigator-sponsored, and real-world evidence studies from concept and protocol development through study completion and publication.

• Develop clinical study protocols, Clinical Study Reports (CSRs), literature reviews, and other essential clinical and regulatory documents supporting regulatory submissions.

• Lead scientific activities supporting regulatory submissions, including scientific justifications, responses to health-authority questions, and scientific interactions with regulatory agencies.

• Analyze and interpret clinical and scientific evidence to support clinical development, regulatory strategy, evidence generation, and product lifecycle management.

• Collaborate closely with Regulatory Affairs, Quality Assurance, R&D, external experts, and other cross-functional partners to advance clinical development programs.

• Lead the development and review of scientific manuscripts, abstracts, posters, presentations, and other scientific publications.

• Support publication strategies, scientific training, congress presentations, and other activities that communicate and disseminate clinical evidence.

More about you

• Master's degree in Life Sciences, Health Sciences, or another related scientific discipline.
• Minimum 8 years of experience in clinical development, clinical research, Medical Affairs, or Scientific Affairs, including protocol development and scientific writing.
• Demonstrated experience developing clinical study protocols, Clinical Study Reports, regulatory scientific documents, and scientific publications.
• Strong knowledge of ICH-GCP, ISO 14155, FDA regulations, and medical device clinical development.
• Excellent scientific writing, analytical, communication, presentation, and project-management skills.
• Ability to effectively collaborate across global and cross-functional teams and provide scientific leadership to complex programs.
• Ability to travel approximately 15-25% to scientific congresses, investigator meetings, and other study-related activities.

Preferred qualifications include: a PhD or AuD; experience with Class III medical devices, hearing healthcare, or neuromodulation; experience leading cross-functional scientific initiatives or mentoring junior scientists; experience supporting FDA PMA/IDE, EU MDR, or other global regulatory submissions and health-authority interactions; and experience with reference-management and statistical software.

A minimum of 300Mb/sec download and 10Mb/sec upload speed internet connectivity is required to support any remote/hybrid employee functionality at Sonova.

What we offer

• 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
• Additional supplemental life/ad&d coverage available
• Company paid Short/Long-Term Disability coverage (STD/LTD)
• STD/LTD Buy-ups available
• 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.

This role's pay range is between: $114K to $143K DEPENDING ON LOCATION AND EXPERIENCE

How we work

At Sonova, we prioritize the well-being of our employees and foster an inclusive environment that promotes engagement and collaboration. Our team-customized hybrid work model empowers teams to balance individual needs with business goals, offering flexibility and individualized time management. We recognize the importance of life outside of work and strive to create a supportive and motivating workplace where innovation thrives.

Sonova is an equal opportunity employer

We team up. We grow talent. We collaborate with people of diverse backgrounds to win with the best team in the market place. We guarantee every person equal treatment in regard to employment and opportunity for employment, regardless of a candidate's ethnic or national origin, religion, sexual orientation or marital status, gender, genetic identity, age, disability or any other legally protected status.