Clinical Research Specialist

Sonova AG•Santa Clarita, CA

7d•Hybrid

About The Position

The Clinical Research Specialist in the Collaborative Clinical Research team will collaborate with research partners to design and implement post market clinical studies on AB products to improve outcomes in hearing technologies, further the clinical science of cochlear implants and enhance awareness and market acceptance of Advanced Bionics products.

Requirements

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

Nice To Haves

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.

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.

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
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.