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Clinical Research Associate

Advanced Bionics -
Valencia, CA

Apply Now

Job Details

$79,000 - $99,000 a year
1 day ago

Benefits

Paid parental leave
Paid holidays
Disability insurance
Health insurance
Dental insurance
Flexible spending account
Tuition reimbursement
Paid time off
Parental leave
Employee assistance program
Vision insurance
401(k) matching
Opportunities for advancement

Qualifications

Data quality checks
English
Clinical audit and monitoring
ICH guidelines
Bachelor's degree
Data quality monitoring
Biomedical regulatory compliance
Clinical quality assurance standards
FDA regulations

Full Job Description

165196

Clinical Research Associate

Valencia, California – Hybrid

Join Advanced Bionics as a Clinical Research Associate and help support the successful execution of global medical device clinical studies from study start-up through close-out. In this role, you will work closely with investigative sites and cross-functional teams to support high-quality clinical research, maintain regulatory compliance, and contribute to studies that support innovative hearing healthcare technologies.

Responsibilities

Execute clinical studies from site start-up through study close-out in compliance with study protocols, ICH-GCP, ISO 14155, FDA regulations, and applicable regulatory requirements.
Conduct site qualification, initiation, interim monitoring, and close-out visits (SQV, SIV, IMV, and COV).
Support site activation, investigator training, study device accountability, and study close-out activities.
Serve as the primary operational contact for assigned investigative sites and monitor site performance, enrollment, protocol compliance, and data quality.
Identify and escalate study risks and ensure timely resolution of monitoring findings, data queries, protocol deviations, and safety-reporting requirements.
Maintain accurate and inspection-ready clinical documentation, including TMF/eTMF and investigator site files, and support audits and regulatory inspections.
Collaborate with Clinical Trial Management and cross-functional partners to support successful study execution and regulatory submissions.

More about you

Bachelor's degree in Life Sciences, Nursing, Biomedical Engineering, or another related scientific discipline.
Minimum 2 years of clinical research experience, including at least 1 year of independent site monitoring.
Experience managing multiple clinical sites and working with CTMS, EDC, and eTMF systems.
Strong knowledge of ICH-GCP, ISO 14155, FDA regulations, clinical monitoring, site management, and data quality.
Strong organizational, communication, problem-solving, and time-management skills with the ability to independently manage multiple priorities.
Fluent English communication skills, both written and spoken.
Ability to travel approximately 30–50% to study sites, conferences, and other study-related activities.

Preferred qualifications include: a Master's degree or equivalent; ACRP-CRA, ACRP-CP, or SOCRA CCRP certification; experience with Class III medical device clinical trials, global multicenter studies, FDA IDE/PMA or EU MDR clinical studies; and knowledge of Risk-Based Monitoring/RbQM.

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

Don't meet all the criteria? If you’re willing to go all in and learn we'd love to hear from you!

We are looking forward to receiving your application via our online job application platform. For this position only direct applications will be considered. Sonova does not recruit via app, telegram, carrier pigeon or any other format that does not include speaking with an actual human. If you are offered a job without speaking with someone please contact Sonova Human Resources.

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: $79,000 – $99,000. This role is also bonus eligible.

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.

Apply Now

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clinical research associate jobs in ventura county ca

Clinical Research Associate

Senior Clinical Research Associate

Clinical Research Assistant

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Clinical Trial Supply & Logistics Coordinator

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Clinical Research Associate

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More about you

What we offer

How we work

Sonova is an equal opportunity employer

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