Wireless protocol development or testing * Experience in product planning or technical product management Technical Expertise * Deep knowledge of: * 5G NR protocol stack (RRC, MAC, PHY interactions)
Wireless protocol development or testing * Experience in product planning or technical product management Technical Expertise * Deep knowledge of: * 5G NR protocol stack (RRC, MAC, PHY interactions)
Active participation in clinical protocol development, improvement and implementation. The Principal Nuclear Medicine Technologist advanced responsibilities can include, yet are not limited to the ...
Active participation in clinical protocol development, improvement and implementation. The Principal Nuclear Medicine Technologist advanced responsibilities can include, yet are not limited to the ...
The Navigator also participates in quality improvement initiatives, protocol development, annual competencies, EMR management, compliance reviews, and training of new staff.
Quick apply
The Navigator also participates in quality improvement initiatives, protocol development, annual competencies, EMR management, compliance reviews, and training of new staff.
Senior Software Development Engineer
San Jose, CA · On-site
$143K - $189K/yr
Medical
Dental
Vision
Retirement
PTO
FW development and L1 switch protocol development * Code reviews, bug fixes and maintenance of drivers * Review of test plans and unit level testing of drivers * Convert customer requirements and use ...
Senior Software Development Engineer
San Jose, CA · On-site
$143K - $189K/yr
Medical
Dental
Vision
Retirement
PTO
FW development and L1 switch protocol development * Code reviews, bug fixes and maintenance of drivers * Review of test plans and unit level testing of drivers * Convert customer requirements and use ...
Senior Software Development Engineer
Irvine, CA · On-site
$131K - $173K/yr
Medical
Dental
Vision
Retirement
PTO
FW development and L1 switch protocol development * Code reviews, bug fixes and maintenance of drivers * Review of test plans and unit level testing of drivers * Convert customer requirements and use ...
Senior Software Development Engineer
Irvine, CA · On-site
$131K - $173K/yr
Medical
Dental
Vision
Retirement
PTO
FW development and L1 switch protocol development * Code reviews, bug fixes and maintenance of drivers * Review of test plans and unit level testing of drivers * Convert customer requirements and use ...
Active participation in clinical protocol development, improvement and implementation. The Principal Nuclear Medicine Technologist advanced responsibilities can include, yet are not limited to the ...
Active participation in clinical protocol development, improvement and implementation. The Principal Nuclear Medicine Technologist advanced responsibilities can include, yet are not limited to the ...
Nurse Navigator
Fremont, CA · On-site
$61.30 - $82.75/hr
The Navigator also participates in quality improvement initiatives, protocol development, annual competencies, EMR management, compliance reviews, and training of new staff.
Nurse Navigator
Fremont, CA · On-site
$61.30 - $82.75/hr
The Navigator also participates in quality improvement initiatives, protocol development, annual competencies, EMR management, compliance reviews, and training of new staff.
Medical Device Study Director/ Veterinary Surgeon
Carlsbad, CA · On-site
Medical
Dental
Vision
Life
Retirement
Proficiency in surgical procedures, dosing, and sampling techniques will be crucial to facilitate protocol development and enhance preclinical studies. Primary Responsibilities This position requires ...
Medical Device Study Director/ Veterinary Surgeon
Carlsbad, CA · On-site
Medical
Dental
Vision
Life
Retirement
Proficiency in surgical procedures, dosing, and sampling techniques will be crucial to facilitate protocol development and enhance preclinical studies. Primary Responsibilities This position requires ...
Clinical Project Manager II - Early Phase Virology /Healthy Volunteer Studies (Sponsor Dedicated...
Medical
Dental
Vision
Retirement
PTO
Lead operational activities across the full study lifecycle, including protocol development, study start-up, study conduct, database lock, and CSR completion. * Oversee dose-escalation activities and ...
Clinical Project Manager II - Early Phase Virology /Healthy Volunteer Studies (Sponsor Dedicated...
Medical
Dental
Vision
Retirement
PTO
Lead operational activities across the full study lifecycle, including protocol development, study start-up, study conduct, database lock, and CSR completion. * Oversee dose-escalation activities and ...
Nurse Navigator
$61.30 - $82.75/hr
The role utilizes nursing best practices to ensure high-quality, patient-centered care The Navigator also participates in quality improvement initiatives, protocol development, annual competencies ...
Nurse Navigator
$61.30 - $82.75/hr
The role utilizes nursing best practices to ensure high-quality, patient-centered care The Navigator also participates in quality improvement initiatives, protocol development, annual competencies ...
Medical Device Study Director/ Veterinary Surgeon
Carlsbad, CA · On-site
$155K - $165K/yr
Medical
Dental
Vision
Life
Retirement
Proficiency in surgical procedures, dosing, and sampling techniques will be crucial to facilitate protocol development and enhance preclinical studies. Primary Responsibilities: This position ...
Quick apply
Medical Device Study Director/ Veterinary Surgeon
Carlsbad, CA · On-site
$155K - $165K/yr
Medical
Dental
Vision
Life
Retirement
Proficiency in surgical procedures, dosing, and sampling techniques will be crucial to facilitate protocol development and enhance preclinical studies. Primary Responsibilities: This position ...
Clinical Project Manager II - Early Phase Virology /Healthy Volunteer Studies (Sponsor Dedicated - U
Foster City, CA · On-site +1
Medical
Dental
Vision
Retirement
PTO
Lead operational activities across the full study lifecycle, including protocol development, study start-up, study conduct, database lock, and CSR completion. * Oversee dose-escalation activities and ...
Clinical Project Manager II - Early Phase Virology /Healthy Volunteer Studies (Sponsor Dedicated - U
Foster City, CA · On-site +1
Medical
Dental
Vision
Retirement
PTO
Lead operational activities across the full study lifecycle, including protocol development, study start-up, study conduct, database lock, and CSR completion. * Oversee dose-escalation activities and ...
Medical Director, Clinical Development-Rheumatology
San Diego, CA · On-site
Retirement
PTO
Clinical Development & Research - MD Job Category: Scientific/Technology All Job Posting Locations ... Develop and review clinical documents, including study concepts, protocols, investigator brochures ...
Medical Director, Clinical Development-Rheumatology
San Diego, CA · On-site
Retirement
PTO
Clinical Development & Research - MD Job Category: Scientific/Technology All Job Posting Locations ... Develop and review clinical documents, including study concepts, protocols, investigator brochures ...
Medical Director, Clinical Development - Oncology
South San Francisco, CA · On-site
$240K - $300K/yr
Contribute meaningfully to clinical development plans (CDPs) and clinical trial protocols. * Analyze and interpret clinical trial data; provide medical input for clinical study reports and regulatory ...
Medical Director, Clinical Development - Oncology
South San Francisco, CA · On-site
$240K - $300K/yr
Contribute meaningfully to clinical development plans (CDPs) and clinical trial protocols. * Analyze and interpret clinical trial data; provide medical input for clinical study reports and regulatory ...
Contribute meaningfully to clinical development plans (CDPs) and clinical trial protocols. * Analyze and interpret clinical trial data; provide medical input for clinical study reports and regulatory ...
Contribute meaningfully to clinical development plans (CDPs) and clinical trial protocols. * Analyze and interpret clinical trial data; provide medical input for clinical study reports and regulatory ...
VP, Clinical Development
Medical
Dental
Vision
PTO
Maintains an active, hands-on role in clinical strategy and execution, directly contributing to protocol development, study design decisions, data interpretation, and cross-functional problem solving ...
VP, Clinical Development
Medical
Dental
Vision
PTO
Maintains an active, hands-on role in clinical strategy and execution, directly contributing to protocol development, study design decisions, data interpretation, and cross-functional problem solving ...
VP, Clinical Development
Irvine, CA · On-site
Medical
Dental
Vision
PTO
Maintains an active, hands-on role in clinical strategy and execution, directly contributing to protocol development, study design decisions, data interpretation, and cross-functional problem solving ...
VP, Clinical Development
Irvine, CA · On-site
Medical
Dental
Vision
PTO
Maintains an active, hands-on role in clinical strategy and execution, directly contributing to protocol development, study design decisions, data interpretation, and cross-functional problem solving ...
Medical Director, Clinical Development-Rheumatology
San Diego, CA · On-site
Retirement
PTO
Clinical Development & Research - MD Job Category: Scientific/Technology All Job Posting Locations ... Develop and review clinical documents, including study concepts, protocols, investigator brochures ...
Medical Director, Clinical Development-Rheumatology
San Diego, CA · On-site
Retirement
PTO
Clinical Development & Research - MD Job Category: Scientific/Technology All Job Posting Locations ... Develop and review clinical documents, including study concepts, protocols, investigator brochures ...
Medical Director, Clinical Development - Oncology
South San Francisco, CA · On-site
$240K - $300K/yr
Contribute meaningfully to clinical development plans (CDPs) and clinical trial protocols. * Analyze and interpret clinical trial data; provide medical input for clinical study reports and regulatory ...
Quick apply
Medical Director, Clinical Development - Oncology
South San Francisco, CA · On-site
$240K - $300K/yr
Contribute meaningfully to clinical development plans (CDPs) and clinical trial protocols. * Analyze and interpret clinical trial data; provide medical input for clinical study reports and regulatory ...
Clinical Research Specialist I - Oncology & Clinical Research
Los Angeles, CA · On-site
$31.75 - $53.98/hr
Support investigator-initiated research, including protocol development, case report forms, study documentation, budgets, and research committee coordination. * Coordinate research activities across ...
Clinical Research Specialist I - Oncology & Clinical Research
Los Angeles, CA · On-site
$31.75 - $53.98/hr
Support investigator-initiated research, including protocol development, case report forms, study documentation, budgets, and research committee coordination. * Coordinate research activities across ...
Protocol Development information
See California salary details
$28.6K - $33.3K
7% of jobs
$33.3K - $38K
8% of jobs
$42K is the 25th percentile. Wages below this are outliers.
$38K - $42.6K
11% of jobs
$42.6K - $47.3K
14% of jobs
The median wage is $49.7K / yr.
$47.3K - $51.9K
19% of jobs
$51.9K - $56.6K
13% of jobs
$58K is the 75th percentile. Wages above this are outliers.
$56.6K - $61.3K
12% of jobs
$61.3K - $65.9K
8% of jobs
$65.9K - $70.6K
4% of jobs
$70.6K - $75.3K
3% of jobs
$75.3K - $79.9K
1% of jobs
$28.6K
$52.7K
$79.9K
How much do protocol development jobs pay per year?
What is the difference between Protocol Development vs Clinical Research Associate?
| Aspect | Protocol Development | Clinical Research Associate |
|---|---|---|
| Primary Role | Designs and develops clinical trial protocols | Monitors clinical trials to ensure compliance and data integrity |
| Required Skills | Knowledge of clinical trial design, regulatory guidelines, and writing skills | Monitoring skills, regulatory knowledge, and communication skills |
| Work Environment | Typically in planning, development, and regulatory teams | On-site or remote monitoring at clinical trial sites |
| Certifications | Often requires knowledge of GCP, regulatory affairs | GCP certification often preferred |
While Protocol Development focuses on creating and designing clinical trial protocols, Clinical Research Associates are responsible for monitoring and ensuring trial compliance at sites. Both roles are essential in clinical research but differ in their core responsibilities and work environments.
What are the key skills and qualifications needed to thrive in protocol development, and why are they important?
What is protocol development?
What are the main challenges someone might face when starting in a protocol development role?
What are popular job titles related to Protocol Development jobs in California?
For Protocol Development jobs in California, the most frequently searched job titles are:
What job categories do people searching Protocol Development jobs in California look for?
The top searched job categories for Protocol Development jobs in California are:

Full-time
Posted 15 days ago
Keysight Technologies rating
8.1
Based on 20 frontline employees who took The Breakroom Quiz
49th of 157 rated electronics manufacturers
Job description
Keysight is at the forefront of technology innovation, delivering breakthroughs and trusted insights in electronic design, simulation, prototyping, test, manufacturing, and optimization. Our ~16,800 employees create world-class solutions in communications, 5G, automotive, energy, quantum, aerospace, defense, and semiconductor markets for customers in over 100 countries. Learn more about what we do.
Our award-winning culture embraces a bold vision of where technology can take us and a passion for tackling challenging problems with industry-first solutions. We believe that when people feel a sense of belonging, they can be more creative, innovative, and thrive at all points in their careers.
This role is that of a technical leader that blends standards adn product planning responsibilities. The individual must be able to drive innovation and influence in 3GPP standardization for 6G wireless protocol test solutions, while also bringing the right insights into product planning, and to shaping the product strategy and roadmap.
Responsibilities
- Actively contribute to and participate in 3GPP (RAN, SA, CT or other working groups) with high-impact technical proposals
- Create and run simulations as necessary in network and device protocols, channel modeling and other relevant areas in order to support 3GPP contributions
- Influence standard evolution aligned with company technology and product strategy
- Build strong relationships with ecosystem players (OEMs, chipset vendors, operators)
- Represent the company as a recognized thought leader in industry forums
- Partner with Planning and R&D functions to prioritize features based on technical feasibility and business impact
- Cultivate a bird’s eye view and perspective of the industry trends, looking into the 3-5 year horizons, and mapping those insights into broad based product strategy
- Influence product roadmap for wireless protocol test platforms (UE, network, and core testing)
- Partner with R&D to prioritize features based on technical feasibility and business impact
- Translate technology priorities into concrete technical requirements
- Collaborate with other functions such as R&D, Go-to-market and Sales
- Support key customer engagements
Qualifications
Education
- Master’s or PhD in Electrical Engineering, Telecommunications, or related field
Experience
- 12+ years in wireless communications, with strong focus on:
- 3GPP standardization contributions
- Wireless protocol development or testing
- Experience in product planning or technical product management
Technical Expertise
- Deep knowledge of:
- 5G NR protocol stack (RRC, MAC, PHY interactions)
- Leading 6G technology candidates and trends
- LTE and legacy technologies
- Core network signaling (5GC, EPC)
- Strong understanding of:
- Conformance and interoperability testing
- Test methodologies and automation
- Familiarity with:
- Network and device simulators, protocol analyzers, and lab test systems
Business & Strategic Skills
- Ability to connect standards evolution to commercial product opportunities
- Strong analytical skills for market and competitive analysis
- Experience defining product requirements and influencing roadmap decisions
Careers Privacy Statement***Keysight is an Equal Opportunity Employer.***
Qualifications:Education
- Master’s or PhD in Electrical Engineering, Telecommunications, or related field
Experience
- 12+ years in wireless communications, with strong focus on:
- 3GPP standardization contributions
- Wireless protocol development or testing
- Experience in product planning or technical product management
Technical Expertise
- Deep knowledge of:
- 5G NR protocol stack (RRC, MAC, PHY interactions)
- Leading 6G technology candidates and trends
- LTE and legacy technologies
- Core network signaling (5GC, EPC)
- Strong understanding of:
- Conformance and interoperability testing
- Test methodologies and automation
- Familiarity with:
- Network and device simulators, protocol analyzers, and lab test systems
Business & Strategic Skills
- Ability to connect standards evolution to commercial product opportunities
- Strong analytical skills for market and competitive analysis
- Experience defining product requirements and influencing roadmap decisions
Careers Privacy Statement***Keysight is an Equal Opportunity Employer.***
Education:UNAVAILABLEEmployment Type: UNAVAILABLEWhat Keysight Technologies employees say
Pay
Benefits
Hours and flexibility
Workplace
Get the full story on Breakroom
About Keysight Technologies
Sourced by ZipRecruiter
Industry
Electrical equipment, appliance, and component manufacturing
Company size
10,000+ Employees
Headquarters location
Santa Rosa, CA, US
Year founded
1937