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Siv Jobs in California (NOW HIRING)

Shifamed

Sr. Field Clinical Specialist

Los Gatos, CA

$120K - $175K/yr

Participate with the clinical monitors during the site training (SQV/SIV) and collect staff, including physician, training records. * Work closely with the company's R amp;D Engineers to obtain ...

Shifamed

Sr. Field Clinical Specialist

Los Gatos, CA · On-site

$120K - $175K/yr

Participate with the clinical monitors during the site training (SQV/SIV) and collect staff, including physician, training records. * Work closely with the company's R&D Engineers to obtain latest ...

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All JobsSiv JobsSiv Jobs in California

Siv information

See California salary details

$5

$90

$189

How much do siv jobs pay per hour?

As of Aug 27, 2026, the average hourly pay for siv in California is $90.25, according to ZipRecruiter salary data. Most workers in this role earn between $51.25 and $189.81 per hour, depending on experience, location, and employer.

What is a siv?

Siv is not a widely recognized job title, and its meaning may vary depending on the industry or company. It could be an abbreviation or a specialized role within a specific field. If you have more context, such as the industry or organization, it would be easier to determine the exact responsibilities and qualifications for a Siv job.

What are some common challenges faced by civil engineers when working on large infrastructure projects?

Civil engineers often encounter challenges such as coordinating with multidisciplinary teams, managing tight project deadlines, and addressing unexpected site or regulatory issues. Effective communication with contractors, architects, and government agencies is crucial to ensure project goals are met. Additionally, adapting to changes in project scope or environmental conditions requires strong problem-solving skills and flexibility. Staying organized and proactive can help civil engineers navigate these challenges successfully.

What are the key skills and qualifications needed to thrive as a civil engineer, and why are they important?

To thrive as a Civil Engineer, you need a solid understanding of structural analysis, mathematics, and engineering principles, typically supported by a bachelor’s degree in civil engineering and professional licensure (PE). Familiarity with technical tools such as AutoCAD, Civil 3D, and project management software is highly valued. Strong problem-solving abilities, teamwork, and effective communication set top performers apart in this field. These competencies are essential for ensuring safe, efficient, and sustainable infrastructure projects that meet regulatory and client requirements.

What is the difference between Siv vs Data Analyst?

AspectSivData Analyst
Required CredentialsTypically requires certifications in security, networking, or specific Siv toolsUsually requires a degree in statistics, computer science, or related fields
Work EnvironmentPrimarily in security operations centers, IT departments, or cybersecurity firmsOften in business, finance, or tech companies analyzing data sets
Employer & Industry UsageUsed by cybersecurity teams, IT departments, and government agenciesEmployed across industries like finance, marketing, healthcare, and tech

While both Siv and Data Analysts work with technical data, Siv focuses on security and network monitoring, whereas Data Analysts analyze data to inform business decisions. Their credentials, work environments, and industry applications differ, making each role specialized in its domain.

What are popular job titles related to Siv jobs in California?

For Siv jobs in California, the most frequently searched job titles are:

What job categories do people searching Siv jobs in California look for?

The top searched job categories for Siv jobs in California are:

Siv jobs near you
Infographic showing various Siv job openings in California as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $187,723 per year, or $90.3 per hour.

Clinical Operations Manager

ExThera Medical

Martinez, CA • On-site

Full-time

Re-posted 26 days ago

Job description

A strategic and hands-on Clinical Operations Manager responsible for overseeing clinical trials for medical devices while driving process remediation and operational excellence. This role requires a creative, resourceful, and flexible leader who can prioritize effectively, build structure where needed, and ensure clinical studies are conducted in full compliance with applicable regulatory standards.
Clinical Trial Leadership & Execution
  • Manage sponsor-led clinical trials for medical devices across the U.S. and EU.
  • Ensure all clinical studies are conducted in adherence to study protocols, ICH/GCP guidelines, and region specific regulations.
  • Direct protocol development and finalization in collaboration with cross-functional teams.
Process Improvement & TMF Remediation
  • Assess, remediate, and optimize clinical processes and work instructions to align with regulatory requirements, industry best practices, and organizational needs.
  • Assess Trial Master File(s) against applicable regulations and industry best practices.  As needed remediate structure of Trial Master File(s) and as applicable records to ensure audit readiness/ preparedness across studies.
Regulatory & Compliance Oversight
  • Serve as point of contact for IRB/EC submissions and correspondence (including central IRBs).
  • Oversee the creation and execution of clinical trial activities in accordance with Good Clinical Practices. Ensure compliance of clinical trials with national and international regulatory requirements and co-monitoring the assigned clinical trial following company SOPs.
  • Oversee preparation and submission of study-level regulatory documents
  • Contribute to validation plans and clinical performance study plans.
  • Perform periodic QC of the TMF

Site & Study Management
  • Proactive identification and management of study related risks
  • Responsible for developing and managing study related plans, processes including; Investigator agreements (CTA), CRFs, monitoring plan, data management, safety monitoring
  • Lead development and management of clinical trial documents including (but not limited to) protocols, Case Report Forms (CRFs), consent documents, confidentiality agreements.
  • Contribute to site identification, feasibility, and selection for clinical studies.
  • Oversee site initiation, monitoring, and close-out activities (SQV, SIV, IMV, COV) as required.
  • Develop and deliver training materials for internal teams, CROs, and study sites (e.g., protocols, device training, SIV presentations).
Leadership & Communication
  • Provide regular clinical program updates to executive leadership and project teams.
  • Foster a culture of accountability and continuous improvement.
  • All other duties as assigned
Qualifications
  • Bachelor’s degree or equivalent in life science
  • Minimum of 7+ years preferred of clinical project management experience in conducting clinical trials in sponsor medical device organization, preferably Class III devices
  • A solid understanding of the ICH guidelines/GCP
  • Experience interacting with regulators, including FDA
  • Ability to travel to visit clinical sites and for study meetings. Amount will vary upon project needs
  • Demonstrated ability to lead teams and work in a fast-paced team environment
  • Ability to successfully engage and work collaboratively with sites and internal teams
  • Excellent written and oral communication skills
     

 

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