Sonova

2 months ago

Senior Manager, Clinical Trials (Valencia (CA), United States)

✓ Verified Job

Canonical indexed version, validated from employer's careers page.

Source: Company careers pageValidated by: Fursa AI

Last checked: 12 hours agoStatus: Live

Job Summary

Lead end-to-end late-phase and pivotal clinical trials for medical devices across multi-country sites, ensuring strategic program direction, regulatory readiness, and high-quality data and outcomes within budget and timelines.

Location: United States

Workplace: Hybrid

Employment Type: Full time

Job Function: Laboratory & Clinical Operations

Seniority: Sr. Manager level

Key Responsibilities

•Own the strategic planning, oversight, and accountability for complex, multi-country clinical trials for medical devices in compliance with ICH E6 GCP, ISO 14155, FDA, and EU MDR regulations, within budget and timelines
•Serve as the primary clinical subject matter expert and single study owner — holding full decision-making authority across all trial activities, driving the strategic direction of clinical development programs, and ensuring alignment with business objectives
•Lead and develop key study documents including protocols, ICFs, EDC specifications, statistical analysis plans, and study reports; ensure high-quality data collection, statistical integrity, and timely reporting of results
•Hold accountability for global study delivery by directing Clinical Operations, aligning Clinical Evaluation, Medical Affairs, and the Clinical Development team to ensure consistent, compliant, and strategically aligned execution
•Lead strategic vendor selection and governance globally; oversee vendor performance against study requirements, escalating issues and driving accountability to ensure high-quality deliverables

Travel: Medium travel

Pay and Benefits

Salary: USD 131,560 - 164,450 annually

Perks:Health Insurance401kPaid LeaveLife Insurance

Key Requirements

•Bachelor’s degree in science/clinical/healthcare field, or equivalent combined education
•Advanced degree (MS or equivalent); CCRP, CCRA, or PMP certification a plus
•8+ years of hands-on experience leading large, complex Phase 3 or pivotal clinical trials in the US and internationally
•Analytical, organized, adaptable; strong communication and ability to work independently in a matrixed environment
•Proven ability to build relationships with external partners, CROs, and vendors; strong track record in timeline and budget management

Experience:8+ yearsHealthcareClinical trialsMedical devices

Education:Bachelor's

Skills:CommunicationLeadershipProject managementStakeholder managementAnalytical

Certifications:CCRPCCRAPMP

Languages:English

Tech Stack:MS OfficeEDCCTMS

Company Brief

Sonova

Designs, manufactures, and distributes hearing care solutions including hearing aids, cochlear implant accessories, and wireless communication devices, serving audiologists and consumers worldwide through clinics, retail networks, and distribution partners.

Industry: Medical Devices

Company Size: Enterprise (1,001+ employees)

Revenue: USD 1B+

Growth: Public Company

Valuation: Public Company (Market Cap in USD)

Funding: IPO / Publicly Listed

Headquarters: Stäfa, Switzerland

Founded: 1947

Website

Loading job details...

Preparing the role view and application actions.

Sonova

2 months ago

Senior Manager, Clinical Trials (Valencia (CA), United States)

✓ Verified Job

Canonical indexed version, validated from employer's careers page.

Source: Company careers pageValidated by: Fursa AI

Last checked: 12 hours agoStatus: Live

Job Summary

Location: United States

Workplace: Hybrid

Employment Type: Full time

Job Function: Laboratory & Clinical Operations

Seniority: Sr. Manager level

Key Responsibilities

•Own the strategic planning, oversight, and accountability for complex, multi-country clinical trials for medical devices in compliance with ICH E6 GCP, ISO 14155, FDA, and EU MDR regulations, within budget and timelines
•Serve as the primary clinical subject matter expert and single study owner — holding full decision-making authority across all trial activities, driving the strategic direction of clinical development programs, and ensuring alignment with business objectives
•Lead and develop key study documents including protocols, ICFs, EDC specifications, statistical analysis plans, and study reports; ensure high-quality data collection, statistical integrity, and timely reporting of results
•Hold accountability for global study delivery by directing Clinical Operations, aligning Clinical Evaluation, Medical Affairs, and the Clinical Development team to ensure consistent, compliant, and strategically aligned execution
•Lead strategic vendor selection and governance globally; oversee vendor performance against study requirements, escalating issues and driving accountability to ensure high-quality deliverables

Travel: Medium travel

Pay and Benefits

Salary: USD 131,560 - 164,450 annually

Perks:Health Insurance401kPaid LeaveLife Insurance

Key Requirements

•Bachelor’s degree in science/clinical/healthcare field, or equivalent combined education
•Advanced degree (MS or equivalent); CCRP, CCRA, or PMP certification a plus
•8+ years of hands-on experience leading large, complex Phase 3 or pivotal clinical trials in the US and internationally
•Analytical, organized, adaptable; strong communication and ability to work independently in a matrixed environment
•Proven ability to build relationships with external partners, CROs, and vendors; strong track record in timeline and budget management

Experience:8+ yearsHealthcareClinical trialsMedical devices

Education:Bachelor's

Skills:CommunicationLeadershipProject managementStakeholder managementAnalytical

Certifications:CCRPCCRAPMP

Languages:English

Tech Stack:MS OfficeEDCCTMS

Company Brief

Sonova

Industry: Medical Devices

Company Size: Enterprise (1,001+ employees)

Revenue: USD 1B+

Growth: Public Company

Valuation: Public Company (Market Cap in USD)

Funding: IPO / Publicly Listed

Headquarters: Stäfa, Switzerland

Founded: 1947

Website