Top 3 Senior staff associate Jobs in California

Senior Staff Clinical Quality Associate (Onsite)
Stryker —Fremont, CA
- $115,600 - $238,400 a year
- Full-time
- 5 years
- Bachelor's degree
- In-person
- Health savings account
- AD&D insurance
12h
Senior Product Designer Associate (External Agency Staff)
National Football League —Inglewood, CA
- $2,300 - $3,500 a month
- 5 years
- Office
- Bachelor's degree
Physician (Associate Chief of Staff of Community Care)
US Veterans Health Administration —San Diego, CA
- $228,100 - $400,000 a year
- Online Application
- Hybrid work
- Background check
- Medicine
- Surgery
- Paid holidays
- Relocation assistance
2d

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Senior Product Designer Associate (External Agency Staff)
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Senior Staff Clinical Quality Associate (Onsite)

Stryker -
Fremont, CA

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Job Details

Full-time
$115,600 - $238,400 a year
12 hours ago

Benefits

Health savings account
AD&D insurance
Employee stock purchase plan
Paid holidays
Disability insurance
Health insurance
Dental insurance
401(k)
Flexible spending account
Vision insurance
Prescription drug insurance

Qualifications

Bachelor's degree
Research regulatory compliance

Full Job Description

Why join Stryker?

Looking for a place that values your unique talents? Discover Stryker's award-winning culture.
We are proud to offer you our total rewards package which includes bonuses, healthcare, insurance benefits, retirement programs, wellness programs, as well as service and performance awards – not to mention various social and recreational activities, all of which are location specific.

Job description

We are excited to be named one of the World’s Best Workplaces by Fortune Magazine! We are proud to offer you 12 paid holidays annually. For an overview of our benefits and time off, please follow this link to learn more:US Stryker employee benefits.

Stryker is hiring a Senior Staff Clinical Quality Associate for our Neurovascular division. This is an onsite role based in Fremont, CA or Salt Lake City, UT.

As the Senior Staff Clinical Quality Associate, you will focus on clinical quality, compliance governance, and regulatory readiness across global clinical research activities. You will provide oversight of quality systems, compliance programs, audits, inspections, and clinical processes to ensure clinical services, documentation, and operations align with applicable regulations and quality standards. You will work across functions to identify risks, strengthen controls, and support the continuous improvement of clinical quality programs.

This role provides quality and compliance oversight for clinical research activities, ensuring processes, documentation, systems, and vendor operations remain compliant, inspection-ready, and aligned with global regulatory and quality requirements.

What you will do

Manage clinical quality and compliance programs, establishing milestones, resource plans, and delivery timelines to support on-time execution
Identify, assess, and communicate compliance risks and control strategies to stakeholders across clinical, quality, and business functions
Lead internal and external audit and inspection activities, including preparation, execution, follow-up actions, and documentation management
Participate in regulatory inspections, including inspections of clinical studies conducted by regulatory authorities
Conduct vendor audits and inspections, maintain audit schedules, and monitor supplier compliance with quality requirements
Analyze process deviations, determine corrective actions, and update procedures to maintain compliance with applicable regulations and standards
Develop, maintain, and revise standard operating procedures, work instructions, and quality documentation
Deliver compliance training, provide guidance on clinical quality requirements, and support continuous improvement initiatives across the clinical organization

What you need

Required

Bachelor’s degree
Minimum 7 years of experience in clinical quality, clinical research, quality assurance, compliance, or a related regulated healthcare or life sciences field
Minimum 5 years of experience supporting quality systems, regulatory compliance programs, audits, or inspections
Experience supporting clinical studies conducted within a regulated environment

Preferred

Experience in medical device, pharmaceutical, biotechnology, or clinical research industries
Experience participating in regulatory inspections and audit readiness activities
Experience developing and maintaining standard operating procedures and quality system documentation
Certified Quality Auditor (CQA), Regulatory Affairs Certification (RAC), or comparable quality or compliance certification

US5: $115,600 - $192,600 USD Annual
US30: $143,100 - $238,400 USD Annual

Health benefits include: Medical and prescription drug insurance, dental insurance, vision insurance, critical illness insurance, accident insurance, hospital indemnity insurance, personalized healthcare support, wellbeing program and tobacco cessation program. Financial benefits include: Health Savings Account (HSA), Flexible Spending Accounts (FSAs), 401(k) plan, Employee Stock Purchase Plan (ESPP), basic life and AD&D insurance, and short-term disability insurance. Stryker offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually. Depending on customer requirements employees and new hires in sales and field roles that require access to customer accounts as a function of the job may be required to obtain various vaccinations as an essential function of their role.

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senior staff associate jobs in california

Senior Staff Clinical Quality Associate (Onsite)

Senior Product Designer Associate (External Agency Staff)

Physician (Associate Chief of Staff of Community Care)

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I want to receive the latest job alert for senior staff associate in california

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