VP, Clinical Development
Irvine, CA · On-site
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 ...
Irvine, CA · On-site
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 ...
Irvine, CA · On-site
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 ...
Support investigator-initiated research, including protocol development, case report forms, study documentation, budgets, and research committee coordination. * Coordinate research activities across ...
Support investigator-initiated research, including protocol development, case report forms, study documentation, budgets, and research committee coordination. * Coordinate research activities across ...
Protocol Development & Automation: Design, build, and optimize end-to-end visual data workflows (protocols) and reusable subprotocols within the BIOVIA Pipeline Pilot environment to automate complex ...
Protocol Development & Automation: Design, build, and optimize end-to-end visual data workflows (protocols) and reusable subprotocols within the BIOVIA Pipeline Pilot environment to automate complex ...
Brisbane, CA · On-site
$96K - $131K/yr
Collaborates with Clinical Scientists and provides input into protocols, contributing medical strategic oversight in protocol development (input on inclusion/exclusion and other safety-related ...
Brisbane, CA · On-site
$96K - $131K/yr
Collaborates with Clinical Scientists and provides input into protocols, contributing medical strategic oversight in protocol development (input on inclusion/exclusion and other safety-related ...
Brisbane, CA · On-site
$96K - $131K/yr
Collaborates with Clinical Scientists and provides input into protocols, contributing medical strategic oversight in protocol development (input on inclusion/exclusion and other safety-related ...
Brisbane, CA · On-site
$96K - $131K/yr
Collaborates with Clinical Scientists and provides input into protocols, contributing medical strategic oversight in protocol development (input on inclusion/exclusion and other safety-related ...
Glendora, CA · On-site
$145/hr
Protocol development involvement * Support community OB physicians in patient care Compensation * $145 hourly * Rates shown are all-inclusive and combine an hourly base pay with other potential ...
Glendora, CA · On-site
$145/hr
Protocol development involvement * Support community OB physicians in patient care Compensation * $145 hourly * Rates shown are all-inclusive and combine an hourly base pay with other potential ...
Brisbane, CA · On-site
$162K - $186K/yr
Perform critical review of analytical data, protocols, reports, specifications, and related ... Collaborate in the development and justification of material control strategies and specifications
Brisbane, CA · On-site
$162K - $186K/yr
Perform critical review of analytical data, protocols, reports, specifications, and related ... Collaborate in the development and justification of material control strategies and specifications
Brisbane, CA · On-site
$162K - $186K/yr
Perform critical review of analytical data, protocols, reports, specifications, and related ... Collaborate in the development and justification of material control strategies and specifications
Brisbane, CA · On-site
$162K - $186K/yr
Perform critical review of analytical data, protocols, reports, specifications, and related ... Collaborate in the development and justification of material control strategies and specifications
Irvine, CA · On-site +1
$85K - $117K/yr
Lead and oversees the training of study investigators on protocol and on clinical trial procedures. * Conduct research to develop foundational education material to inform the early development ...
Irvine, CA · On-site +1
$85K - $117K/yr
Lead and oversees the training of study investigators on protocol and on clinical trial procedures. * Conduct research to develop foundational education material to inform the early development ...
Irvine, CA · On-site
$85K - $117K/yr
Lead and oversees the training of study investigators on protocol and on clinical trial procedures. * Conduct research to develop foundational education material to inform the early development ...
Irvine, CA · On-site
$85K - $117K/yr
Lead and oversees the training of study investigators on protocol and on clinical trial procedures. * Conduct research to develop foundational education material to inform the early development ...
Irvine, CA · On-site +1
$85K - $117K/yr
Lead and oversees the training of study investigators on protocol and on clinical trial procedures. * Conduct research to develop foundational education material to inform the early development ...
Irvine, CA · On-site +1
$85K - $117K/yr
Lead and oversees the training of study investigators on protocol and on clinical trial procedures. * Conduct research to develop foundational education material to inform the early development ...
Fremont, CA · On-site
$79K - $105K/yr
Protocol Development: Author robust study protocols, develop data analysis/calculation worksheets, and execute benchtop laboratory testing in strict accordance with approved protocols. * Data ...
Fremont, CA · On-site
$79K - $105K/yr
Protocol Development: Author robust study protocols, develop data analysis/calculation worksheets, and execute benchtop laboratory testing in strict accordance with approved protocols. * Data ...
Independently leads projects to create and develop novel nucleic acid based diagnostic tests; including planning, feasibility testing, protocol development, and optimization * Responsible for ...
Independently leads projects to create and develop novel nucleic acid based diagnostic tests; including planning, feasibility testing, protocol development, and optimization * Responsible for ...
$79K - $105K/yr
Protocol Development: Author robust study protocols, develop data analysis/calculation worksheets, and execute benchtop laboratory testing in strict accordance with approved protocols. * Data ...
$79K - $105K/yr
Protocol Development: Author robust study protocols, develop data analysis/calculation worksheets, and execute benchtop laboratory testing in strict accordance with approved protocols. * Data ...
South San Francisco, CA · On-site
$242.10 - $282.45/hr
Responsibilities include contributing to protocol design, and to clinical development and statistical analysis plans, as well as conducting exploratory analyses to inform development decisions and ...
South San Francisco, CA · On-site
$242.10 - $282.45/hr
Responsibilities include contributing to protocol design, and to clinical development and statistical analysis plans, as well as conducting exploratory analyses to inform development decisions and ...
... study protocol development, reviewing of informed consent forms, case report forms, monitoring plans, and other study materials • Maintains regular contact with relevant departments (e.g ...
... study protocol development, reviewing of informed consent forms, case report forms, monitoring plans, and other study materials • Maintains regular contact with relevant departments (e.g ...
Emeryville, CA · On-site
$180 - $250/hr
Generate, review, and/or approve study protocols, development reports, and manufacturing batch records * Manage developmental stage-appropriate analytical activities * Communicate CMC strategy and ...
Emeryville, CA · On-site
$180 - $250/hr
Generate, review, and/or approve study protocols, development reports, and manufacturing batch records * Manage developmental stage-appropriate analytical activities * Communicate CMC strategy and ...
Hayward, CA · On-site
$135K - $155K/yr
Lead execution of preclinical studies, including protocol development, experimental design input, data collection, and report authorship. * Develop and refine benchtop, ex vivo, and in vivo models to ...
Hayward, CA · On-site
$135K - $155K/yr
Lead execution of preclinical studies, including protocol development, experimental design input, data collection, and report authorship. * Develop and refine benchtop, ex vivo, and in vivo models to ...
Contribute to quality assurance, performance improvement, and clinical/research protocol development. * Demonstrate and instruct advanced procedures. * Mentor and train less experienced technologists.
Quick apply
Contribute to quality assurance, performance improvement, and clinical/research protocol development. * Demonstrate and instruct advanced procedures. * Mentor and train less experienced technologists.
Experience in either starting a study up, maintenance phase, or study close-out Experience with development of prospective site-selection criteria Protocol development experience Maintain a working ...
Experience in either starting a study up, maintenance phase, or study close-out Experience with development of prospective site-selection criteria Protocol development experience Maintain a working ...
$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
| 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.
For Protocol Development jobs in California, the most frequently searched job titles are:
The top searched job categories for Protocol Development jobs in California are:

Full-time
Medical, Dental, Vision, PTO
Re-posted 25 days ago
About the Role
The Vice President, Clinical Development - provides strategic and scientific leadership for all clinical programs, overseeing trial direction, design, execution and data analysis and interpretation from first-in-human through proof-of-concept, and approval. While anchored in early clinical development, this leader holds accountability across the full clinical development continuum - from first-in-human through late-stage trials and registration - ensuring seamless strategic continuity as programs advance. A primary focus of this role is to create an adaptable early development clinical strategy to support innovative trials that require creative, forward-thinking approaches to study design, endpoints, and operational strategy. Equally critical is building and sustaining a high-performing clinical development organization: attracting top talent, cultivating the next generation of clinical leaders, and fostering a culture of scientific rigor, accountability, and continuous learning. This leader will challenge conventional paradigms, applying rigorous scientific judgment and out-of-the-box thinking to inform key development decisions across all stages.
This position will oversee Clinical Sciences, Clinical Operations, Biostats/Data Mgmt and will partner cross-functionally with Regulatory Affairs, Translational Sciences, Medical Affairs, Commercial, Innovation lab, Finance and Legal to drive efficient and scientifically rigorous clinical work. This person will also work closely with the Business Development team and will be involved in clinical due diligence.
Let's talk about some of the key responsibilities of the role:
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 that can rapidly and robustly assess proof-of-concept in early trials
Factors for Success:
Leadership Competencies - This role requires mastery of the Tarsus Leadership Competencies for Leading Teams, including:
A Few Other Details Worth Mentioning:
At Tarsus, we understand the importance of attracting and retaining top talent. The expected base pay range for this position is $300,000 - $420,000 plus bonus, stock equity, and comprehensive benefits. The base pay range reflects the target range for this position, but individual pay will be determined by additional factors such as job-related skills, experience and relevant education or training. Our benefits include health, dental and vision insurance benefits to ensure your well-being. We believe in work-life balance and offer generous paid time off, including vacation, holidays, and personal days. For more details regarding Tarsus benefits, please visit: https://eb.alliant.com/26tarsusbenefitssnapshot.
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Pharmaceutical and medicine manufacturing
11 - 50 Employees
Irvine, CA, US
2017