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Cta Pharmaceutical Jobs (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 ... Experience supporting clinical studies within the biotechnology, pharmaceutical, medical device, or ...

Spyglass Pharma

Clinical Trial Associate

Aliso Viejo, CA · On-site

$35.50 - $48.50/hr

... CTA of experience in clinical affairs within the pharmaceutical or medical device industry, with a preference on drug and drug/device combination products. (A commensurate combination of education ...

Spyglass Pharma

Clinical Trial Associate

Aliso Viejo, CA · On-site

$35.50 - $48.50/hr

... CTA of experience in clinical affairs within the pharmaceutical or medical device industry, with a preference on drug and drug/device combination products. (A commensurate combination of education ...

Spyglass Pharma

Clinical Trial Associate

Aliso Viejo, CA · On-site

$35.50 - $48.50/hr

... CTA of experience in clinical affairs within the pharmaceutical or medical device industry, with a preference on drug and drug/device combination products. (A commensurate combination of education ...

Spyglass Pharma

Clinical Trial Associate

Aliso Viejo, CA · On-site

$90K - $110K/yr

... CTA of experience in clinical affairs within the pharmaceutical or medical device industry, with a preference on drug and drug/device combination products. (A commensurate combination of education ...

Glaukos

Clinical Trials Associate II

Aliso Viejo, CA · On-site

$35.50 - $48.50/hr

Founded in 1998, Glaukos Corporation is an ophthalmic pharmaceutical and medical technology company ... CTA is responsible for effective communication with clinical trial sites * Assists with analyses of ...

New

Glaukos

Clinical Trials Associate II

Aliso Viejo, CA · On-site

$35.50 - $48.50/hr

Founded in 1998, Glaukos Corporation is an ophthalmic pharmaceutical and medical technology company ... CTA is responsible for effective communication with clinical trial sites * Assists with analyses of ...

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How much do cta pharmaceutical jobs pay per hour?

As of Aug 9, 2026, the average hourly pay for cta pharmaceutical in the United States is $19.78, according to ZipRecruiter salary data. Most workers in this role earn between $17.79 and $21.88 per hour, depending on experience, location, and employer.

What does a clinical trial assistant do in the pharmaceutical industry?

A CTA (Clinical Trial Assistant) in the pharmaceutical industry supports the planning, execution, and documentation of clinical trials. They handle administrative tasks such as maintaining trial master files, tracking regulatory documents, and coordinating communication between study sites and sponsors. CTAs play a key role in ensuring that clinical trials run smoothly and comply with regulatory requirements. Their work helps facilitate the collection of data needed for the development and approval of new medications.

What is the difference between Cta Pharmaceutical vs Pharmaceutical Sales Representative?

AspectCta PharmaceuticalPharmaceutical Sales Representative
Required CredentialsCertification in clinical trial administration, relevant pharmaceutical knowledgeSales and marketing certifications, knowledge of pharmaceutical products
Work EnvironmentClinical settings, hospitals, research facilitiesOffices, client meetings, healthcare provider visits
Employer & Industry UsagePharmaceutical companies, clinical research organizationsPharmaceutical companies, medical device firms

While both roles operate within the pharmaceutical industry, Cta Pharmaceutical focuses on clinical trial administration and research, whereas Pharmaceutical Sales Representatives primarily promote and sell pharmaceutical products to healthcare providers. Understanding these differences helps job seekers identify the right career path based on their skills and interests.

What are common challenges clinical trial assistants face in pharmaceutical research, and how are they addressed?

CTAs in pharmaceutical research frequently encounter challenges such as managing large volumes of documentation, ensuring regulatory compliance, and coordinating communication among diverse stakeholders. These challenges are typically addressed through strong organizational skills, adherence to standardized processes, and the use of specialized clinical trial management systems. CTAs also benefit from ongoing training and close collaboration with clinical research associates, project managers, and regulatory teams to maintain study efficiency and data integrity.

What key skills and qualifications are needed to thrive as a clinical trial assistant in the pharmaceutical industry?

To thrive as a Clinical Trial Assistant (CTA) in the pharmaceutical industry, you need a foundational understanding of clinical trial processes, documentation, and regulatory requirements, often supported by a science degree or relevant certification. Familiarity with electronic trial master file (eTMF) systems, clinical trial management systems (CTMS), and Good Clinical Practice (GCP) guidelines is typically required. Attention to detail, organizational skills, and effective communication are vital soft skills for managing trial documentation and collaborating with cross-functional teams. These skills ensure accurate trial records, regulatory compliance, and smooth coordination across clinical research activities.
More about Cta Pharmaceutical jobs
What states have the most Cta Pharmaceutical jobs? States with the most job openings for Cta Pharmaceutical jobs include:
What job categories do people searching Cta Pharmaceutical jobs look for? The top searched job categories for Cta Pharmaceutical jobs are:
Cta Pharmaceutical jobs near you
Infographic showing various Cta Pharmaceutical job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 14% Part Time, 1% Temporary, 4% Contract, and 1% Nights. Highlights an 89% Physical, 2% Hybrid, and 9% Remote job distribution, with an average salary of $41,139 per year, or $19.8 per hour.

Sr CTA - Autoimmune

Solomon Page

San Diego, CA • On-site

$35 - $48/hr

Contractor

Medical, Dental, Retirement

Re-posted 3 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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