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Cta Jobs in California (NOW HIRING)

Solomon Page

Sr CTA - Autoimmune

San Diego, CA · On-site

$35 - $48/hr

Our client is looking to fill the role of CTA. The Senior Clinical Trial Associate supports the operational execution of clinical studies by partnering with internal Clinical Operations team, study ...

Terravanta Inc

Office Engineer

Los Angeles, CA · On-site

$80K - $87K/yr

The CTA Curbside Improvement Program reports to CTA Curbside Improvement Project Manager and is responsible for assisting the CTA Curbside Improvement Project Manager with managing the scope ...

Atlas

Office Engineer

Riverside, CA · On-site

The CTA Curbside Improvement Program reports to CTA Curbside Improvement Project Manager and is responsible for assisting the CTA Curbside Improvement Project Manager with managing the scope ...

Atlas

Office Engineer

Riverside, CA · On-site

The CTA Curbside Improvement Program reports to CTA Curbside Improvement Project Manager and is responsible for assisting the CTA Curbside Improvement Project Manager with managing the scope ...

Spyglass Pharma

Clinical Trial Associate

Irvine, CA · On-site

$35.75 - $48.75/hr

The CTA is responsible for executing the tasks on the clinical team throughout the clinical trial. This position has the responsibility of supporting the clinical departmentin executing and ...

California Teachers Association

Supervisor

Norco, CA · On-site

Coordinates execution of regional resource center lease agreements with CTA Property Management Supervisor and regional management. * Coordinates new location and office layout design and upgrading ...

New

Spyglass Pharma

Clinical Trial Associate

Aliso Viejo, CA · On-site

$35.50 - $48.50/hr

The CTA is responsible for executing the tasks on the clinical team throughout the clinical trial. This position has the responsibility of supporting the clinical department in executing and ...

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See California salary details

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How much do cta jobs pay per year?

As of Aug 19, 2026, the average yearly pay for cta in California is $114,954.00, according to ZipRecruiter salary data. Most workers in this role earn between $89,300.00 and $134,200.00 per year, depending on experience, location, and employer.

What is a CTA?

A Clinical Trial Associate (CTA) is a professional who supports clinical research studies by managing documentation, coordinating trial activities, and ensuring regulatory compliance. They assist clinical research teams with tasks like maintaining trial records, organizing investigator files, and facilitating communication between stakeholders. CTAs play a crucial role in ensuring the smooth execution of clinical trials while adhering to industry guidelines and protocols.

What are the typical daily responsibilities of a CTA?

As a Clinical Trial Assistant, your daily responsibilities often include maintaining trial documentation, supporting study start-up activities, coordinating meetings, and tracking study progress. You will assist both clinical research associates and project managers by organizing files, preparing documents for regulatory submissions, and managing communications with trial sites. CTAs also help ensure that data is accurately filed within clinical trial management systems and that studies adhere to compliance standards. This role is highly collaborative, requiring regular interaction with cross-functional teams and external partners, making strong organizational and communication skills essential.

What are the key skills and qualifications needed to thrive in the CTA position, and why are they important?

To thrive as a CTA (Clinical Trial Assistant), you need a solid understanding of clinical research processes, strong organizational abilities, and at least a bachelor's degree in a life science or related field. Familiarity with clinical trial management systems (CTMS), electronic trial master file (eTMF) systems, and Good Clinical Practice (GCP) guidelines is highly beneficial and sometimes required. Exceptional attention to detail, communication skills, and the ability to manage multiple priorities are crucial soft skills for this position. These capabilities ensure accurate documentation, regulatory compliance, and effective support of clinical study teams for successful trial execution.

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

The most popular types of Cta jobs in California are:

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

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

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

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

What cities in California are hiring for Cta jobs?

Cities in California with the most Cta job openings:

Cta jobs near you
Infographic showing various Cta 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 $114,954 per year, or $55.3 per hour.

Sr CTA - Autoimmune

Solomon Page

San Diego, CA • On-site

$35 - $48/hr

Contractor

Medical, Dental, Retirement

Re-posted 14 days ago

Job description

Our client is looking to fill the role of CTA. The Senior Clinical Trial Associate supports the operational execution of clinical studies by partnering with internal Clinical Operations team, study sites, vendors, and CROs. This role is responsible for clinical trial documentation, tracking, vendor coordination, and study support activities to help ensure trials are conducted in compliance with applicable regulations and company procedures.
  • Pay Range: $35-48/hour
  • Location: San Diego, CA

Responsibilities:
  • Support day-to-day clinical trial operations across one or more studies.
  • Maintain and organize Trial Master File (TMF) documentation and track essential study records.
  • Monitor document status and communicate outstanding items to the study team.
  • Track study metrics, enrollment, site activity, and clinical supply information.
  • Assist with vendor, CRO, and site coordination activities.
  • Support invoice tracking, reconciliation, and study budget administration.
  • Identify and communicate study issues, risks, or operational concerns to the clinical team.
  • Assist with review and management of study-related documents and materials.
  • Ensure compliance with applicable regulations, GCP guidelines, SOPs, and study requirements.
  • Perform additional clinical operations activities as assigned.

Required Qualifications:
  • Bachelor's degree in Life Sciences or a related field preferred.
  • Minimum of 3 years of clinical operations or clinical trial support experience.
  • Experience supporting clinical studies within the biotechnology, pharmaceutical, medical device, or CRO industry preferred.
  • Autoimmune experience required
  • Working knowledge of clinical trial processes, documentation, and GCP requirements.
  • Strong organizational skills with exceptional attention to detail.
  • Proficiency with Microsoft Office applications, including Outlook, Word, Excel, and PowerPoint.
  • Strong written and verbal communication skills.
  • Ability to manage multiple priorities and work effectively in a collaborative environment.
If you meet the required qualifications and are interested in this role, please apply today.
The Solomon Page Distinction
Solomon Page offers a comprehensive benefit program for hourly employees. We pride ourselves on offering medical, dental, 401(k), direct deposit and commuter benefits to our employees, including freelancers - which sets us apart in the industries we serve.
About Solomon Page
Founded in 1990, Solomon Page is a specialty niche provider of staffing and executive search solutions across a wide array of functions and industries. The success of Solomon Page reflects an organic growth strategy supported by a highly entrepreneurial culture. Acting as a strategic partner to our clients and candidates, we focus on providing customized solutions and building long-term relationships based on trust, respect, and the consistent delivery of excellent results. For more information and additional opportunities, visit: solomonpage.com and connect with us on Facebook , and LinkedIn .
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