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Cta Pharmaceutical Jobs (NOW HIRING)

Solomon Page

CTA - Oncology

San Diego, CA · On-site

$35 - $48/hr

Our client is looking to fill the role of CTA- Oncology. The Senior Clinical Trial Associate ... Experience supporting clinical studies within the biotechnology, pharmaceutical, medical device, or ...

Solomon Page

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

$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 ...

Medpace, Inc.

Contract Manager

Cincinnati, OH · On-site

$85K - $114K/yr

Develop the study-specific CTA strategy with the Sponsor and internal stakeholders * Develop ... We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and ...

Medpace, Inc.

Experienced Contract Manager

Irving, TX

$82K - $110K/yr

Develop the study-specific CTA strategy with the Sponsor and internal stakeholders * Develop ... We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and ...

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How much do cta pharmaceutical jobs pay per hour?

As of Jul 27, 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 CTA (Clinical Trial Assistant) in the pharmaceutical industry do?

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 is CTA salary?

The salary for a CTA (Clinical Trial Assistant) varies depending on experience, location, and employer, but typically ranges from $40,000 to $60,000 annually. Entry-level positions may start lower, while experienced CTAs or those with specialized skills can earn higher wages. Certifications in clinical research can also influence salary levels.

How much does a clinical trial assistant earn?

A clinical trial assistant typically earns between $40,000 and $60,000 annually, depending on experience, location, and the size of the organization. Entry-level positions may start lower, while experienced assistants with certifications can earn higher salaries. The role often requires familiarity with clinical trial protocols and data management tools.

What is a CTA in pharmaceuticals?

A CTA in pharmaceuticals stands for Clinical Trial Agreement, which is a legal document between a sponsor and a research site that outlines the terms for conducting a clinical trial. It ensures compliance with regulatory standards, protects both parties' interests, and details responsibilities, budgets, and confidentiality requirements for the trial process.

What is a CTA job in healthcare?

A CTA job in healthcare typically refers to a Clinical Trial Assistant, who supports the management of clinical trials by coordinating documentation, tracking study progress, and ensuring compliance with regulatory standards. This role often requires attention to detail, organizational skills, and familiarity with Good Clinical Practice (GCP) guidelines. CTAs work closely with clinical research teams and may use trial management software to perform their duties.

What are some common challenges Clinical Trial Assistants (CTAs) face in pharmaceutical research, and how are they typically 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 (CTA) in the pharmaceutical industry, and why are they important?

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 July 2026, with employment types broken down into 1% Locum Tenens, 2% Internship, 85% Full Time, 4% Part Time, and 8% Contract. Highlights an 89% Physical, 3% Hybrid, and 8% Remote job distribution, with an average salary of $41,139 per year, or $19.8 per hour.
CTA - Oncology

CTA - Oncology

Solomon Page

San Diego, CA • On-site

$35 - $48/hr

Contractor

Posted 23 days ago

Job description

Our client is looking to fill the role of CTA- Oncology. 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.
  • Oncology 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
Our teams, comprised of subject matter experts, develop an interest in your preferences and goals and we act as an advisor for your career advancement. Solomon Page has an extensive network of established clients which allows us to present opportunities that are well-suited to your respective goals and needs - this specialized approach 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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