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Cra Manager Jobs in California (NOW HIRING)

As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. What You Will ...

As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. What You Will ...

The CRA II manages an assigned set of multiple research protocols to assure efficiency and regulatory compliance of the protocol, attending clinic as needed. As a successful candidate, you will:

The CRA II manages an assigned set of multiple research protocols to assure efficiency and regulatory compliance of the protocol, attending clinic as needed. As a successful candidate, you will:

Senior CRA

Long Beach, CA ยท On-site

$110K - $138K/yr

As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. What You Will ...

Senior CRA

Long Beach, CA ยท On-site

$110K - $138K/yr

As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. What You Will ...

As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. What You Will ...

As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. What You Will ...

Showing results 41-60

Cra Manager information

See California salary details

$26.4K

$94.6K

$134.2K

How much do cra manager jobs pay per year?

As of Aug 20, 2026, the average yearly pay for cra manager in California is $94,641.00, according to ZipRecruiter salary data. Most workers in this role earn between $73,931.00 and $114,080.00 per year, depending on experience, location, and employer.

What is a CRA Manager?

A CRA Manager, or Clinical Research Associate Manager, is a professional responsible for overseeing a team of Clinical Research Associates (CRAs) who monitor clinical trials. They ensure that clinical studies are conducted in compliance with regulatory standards, protocols, and company policies. CRA Managers coordinate training, provide performance feedback, and act as a liaison between CRAs, sponsors, and other stakeholders. Their role is critical in maintaining the quality and integrity of clinical research projects.

What are the key skills and qualifications needed to thrive as a CRA Manager?

To thrive as a CRA (Clinical Research Associate) Manager, you need a deep understanding of clinical trial processes, regulatory requirements, and a relevant life sciences degree, often supplemented by experience as a CRA. Familiarity with electronic data capture (EDC) systems, trial management software, and certifications such as ACRP or SOCRA are typically required. Leadership, strong communication, and problem-solving skills help you guide teams and ensure effective collaboration across stakeholders. These skills are crucial for maintaining compliance, ensuring data integrity, and delivering successful clinical trials on time and within budget.

What are some common challenges a CRA Manager faces when overseeing multiple clinical trial sites?

A CRA Manager often encounters challenges with maintaining consistent quality and compliance across various clinical trial sites, as each site may have unique operational practices and resource limitations. Effective communication and coordination between on-site teams, sponsors, and regulatory bodies are crucial to address issues promptly and ensure study timelines are met. Additionally, balancing the workload among Clinical Research Associates (CRAs) and providing adequate training and support can be demanding, especially when managing geographically dispersed teams.

What is the difference between Cra Manager vs Clinical Research Associate?

AspectCra ManagerClinical Research Associate
CredentialsBachelor's or higher in life sciences, often with experience in project managementBachelor's degree in life sciences or related field, often with certification
Work EnvironmentLeads multiple studies, manages teams, oversees project progressMonitors clinical trials at sites, ensures protocol compliance
Employer & IndustryPharmaceutical companies, CROs, biotech firmsPharmaceutical companies, CROs, clinical sites
Search & Comparison IntentHigher-level management, overseeing clinical trialsMonitoring and site management roles

The Cra Manager typically oversees multiple clinical trials, manages teams, and ensures project milestones are met, requiring leadership skills and experience. In contrast, a Clinical Research Associate focuses on monitoring individual trial sites, ensuring compliance with protocols. Both roles are essential in clinical research but differ in scope and responsibilities.

What are the most commonly searched types of Cra jobs in California?

The most popular types of Cra jobs in California are:

What cities in California are hiring for Cra Manager jobs?

Cities in California with the most Cra Manager job openings:

Infographic showing various Cra Manager job openings in California as of August 2026, with employment types broken down into 90% Full Time, 9% Part Time, and 1% Contract. Highlights an 81% Physical, 2% Hybrid, and 17% Remote job distribution, with an average salary of $94,641 per year, or $45.5 per hour.

Cyber Resilience Act (CRA) Compliance Lead

Altera Corporation

San Jose, CA โ€ข On-site

$149K - $215K/yr

Full-time

Posted 13 days ago


Job description

Job Details:
Job Description:
About Altera
At Alteraโ„ข, our independence as the world's largest pure-play FPGA solutions provider gives us the focus, speed, and agility to innovate without compromise. With more than four decades of industry-leading FPGA expertise, our singular mission is to deliver the programmable technologies that help customers differentiate, innovate, and scale across rapidly evolving markets like AI, cloud, networking, and edge. As an independent company, we move faster, invest deeper, and partner more closely-empowering our teams to drive breakthrough innovation and shape the future of the FPGA industry.
About the Role
We are seeking for a Cyber Resilience Act (CRA) Compliance Lead who will establish, govern, and drive the company-wide compliance framework for the European Union Cyber Resilience Act and related product cybersecurity regulatory requirements.
Reporting within the Quality & Reliability organization, this role will serve as the enterprise CRA compliance lead and will coordinate cross-functional activities. The role is responsible for translating regulatory obligations into scalable product lifecycle processes, compliance requirements, governance mechanisms, objective evidence, and conformity documentation. The CRA Compliance Lead will provide independent oversight of compliance while partnering with technical organizations responsible for cybersecurity architecture, product, software and firmware development, vulnerability management, security testing, incident response, vendor management and implementation of cybersecurity controls.
This is a senior role requiring strong knowledge of product cybersecurity regulations, semiconductor and embedded-product lifecycles, quality management systems, risk management, regulatory conformity, and cross-functional program execution.
Key Responsibilities:
CRA Compliance Strategy & Governance
  • Maintain the enterprise CRA compliance framework, governance model, policies, procedures, roles, responsibilities, and decision authorities.
  • Establish traceability model between CRA requirements, cybersecurity risks, product requirements, design controls, verification activities, technical documentation, and conformity evidence.
  • Coordinate alignment with applicable standards and frameworks, including ISO/IEC 27001, IEC 62443, ISO/SAE 21434, ISO 26262, vulnerability management standards, emerging CRA harmonized standards and Altera security requirements.
  • Monitor regulatory developments, delegated acts, implementing guidance, harmonized standards, and industry interpretations that may affect company products or compliance obligations.
  • Partner with cross functional organization to determine product classification, critical-product applicability, conformity assessment pathways and regulatory obligations.
  • Support integration of CRA requirements into product requirement management, product lifecycle management, configuration management, change control, and release-management systems.
  • Establish governance requirements for Software Bill of Materials management and CRA-related software-component traceability.
  • Coordinate assessment of third-party software, intellectual property, software components, and external dependencies that may affect product compliance.
  • Lead development and governance of the CRA conformity-assessment framework, and maintenance of required CRA technical documentation and conformity evidence.
  • Define and drive CRA compliance check and evidence requirements for product concept, architecture, design, implementation, verification, validation, release, production, maintenance, and end-of-support stages.

CRA Compliance Operations & Enablement:
  • Partner with product security on vulnerability escalation, product non-conformity management and external communication
  • Establish CRA compliance metrics, dashboards, risk indicators, and management-reporting mechanisms.
  • Integrate CRA compliance monitoring into applicable QMS audit, management-review, risk-management, and corrective-action processes.
  • Develop CRA training, awareness, role-based competency requirements, and implementation guidance to promote a sustainable compliance culture.
  • Facilitate resolution of complex regulatory, technical, process, and organizational compliance issues.

Salary Range
The pay range below is for Bay Area California only. Actual salary may vary based on a number of factors including job location, job-related knowledge, skills, experiences, trainings, etc. We also offer incentive opportunities that reward employees based on individual and company performance.
$149,100 - $215,925 USD
We use artificial intelligence to screen, assess, or select applicants for the position. Applicants must be eligible for any required U.S. export authorizations.
#LI-MD1
Qualifications:
Minimum Qualifications
  • Bachelor's degree in Engineering, Computer Science, Information Systems, Cybersecurity, Quality, or a related technical field.
  • 10+ years of experience in product compliance, product cybersecurity, quality systems, regulatory compliance, engineering governance, semiconductor product development, or related technical disciplines.
  • 2+ years of experience interpreting and applying product cybersecurity regulations, including the EU Cyber Resilience Act (CRA) and other applicable global product security regulatory requirements.
  • 8+ years of experience leading enterprise or product compliance programs across multiple cross-functional organizations and global geographic locations.
  • 8+ years of experience implementing secure product development lifecycle (Secure SDLC) processes, product cybersecurity risk management, vulnerability management, software component governance (SBOM/open-source governance), and post-market product security compliance.
  • 8+ years of experience managing product lifecycle governance processes, including New Product Introduction (NPI), requirements management, configuration management, engineering change management, product release governance, audit readiness, and compliance evidence management.
  • 8+ years of experience partnering with executive leadership, engineering, legal, quality, security, and product management teams to drive compliance initiatives and influence technical decisions without direct management authority.
  • 8+ years of experience leading complex cross-functional programs requiring executive-level communication, data-driven decision making, stakeholder management, facilitation, and presentation of compliance strategies, risks, and program status to senior leadership.

Preferred Qualifications
  • Experience within the FPGA, semiconductor, embedded systems, electronics, automotive, aerospace, defense, industrial, or technology industries.
  • Experience with semiconductor hardware, embedded firmware, software development tools, intellectual property, reference designs, or complex product ecosystems.
  • Working knowledge of applicable standards and frameworks, such as:
    • IEC 62443, ISO/SAE 21434, ISO/IEC 27001, ISO 9001, AS9100, ISO 26262,IEC 61508
    • NIST Cybersecurity and secure software development Framework, Common Criteria or related product-security assurance frameworks
  • Experience with Software Bill of Materials, 3rd party and open-source software governance, vulnerability-disclosure programs, product security incident response, or cybersecurity conformity assessment.
  • Experience supporting CE marking, EU product regulations, technical-file development, declarations of conformity, or market-surveillance activities.

Job Type:
Regular
Shift:
Shift 1 (United States of America)
Primary Location:
San Jose, California, United States
Additional Locations:
Posting Statement:
All qualified applicants will receive consideration for employment without regard to race, color, religion, religious creed, sex, national origin, ancestry, age, physical or mental disability, medical condition, genetic information, military and veteran status, marital status, pregnancy, gender, gender expression, gender identity, sexual orientation, or any other characteristic protected by local law, regulation, or ordinance.