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Clinical Trial Associate Cta Jobs (NOW HIRING)

Cellectis

Clinical Trial Associate

Manhattan, NY

$36.75 - $50.25/hr

The Clinical Trial Associate (CTA) supports clinical study teams in the execution and oversight of clinical trials under the direction of the Vice President, Development Operations, with day-to-day ...

Cellectis

Clinical Trial Associate

Manhattan, NY · On-site

$36.75 - $50.25/hr

The Clinical Trial Associate (CTA) supports clinical study teams in the execution and oversight of clinical trials under the direction of the Vice President, Development Operations, with day-to-day ...

Spyglass Pharma

Clinical Trial Associate

Aliso Viejo, CA · On-site

$35.50 - $48.50/hr

  • Medical

  • Dental

  • Vision

  • PTO

We are seeking a Clinical Trial Associate (CTA) / Senior CTA to join our team at SpyGlass Pharma ... The CTA is responsible for executing the tasks on the clinical team throughout the clinical trial.

Spyglass Pharma

Clinical Trial Associate

Aliso Viejo, CA · On-site

$90K - $110K/yr

  • Medical

  • Dental

  • Vision

  • PTO

We are seeking a Clinical Trial Associate (CTA) / Senior CTA to join our team at SpyGlass Pharma ... The CTA is responsible for executing the tasks on the clinical team throughout the clinical trial.

Spyglass Pharma

Clinical Trial Associate

Irvine, CA

$35.75 - $48.75/hr

  • Medical

  • Dental

  • Vision

  • PTO

We are seeking a Clinical Trial Associate (CTA) / Senior CTA to join our team at SpyGlass Pharma ... The CTA is responsible for executing the tasks on the clinical team throughout the clinical trial.

Ardelyx

Clinical Trial Associate

Newark, CA · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

The CTA contributes across all phases of the clinical trial lifecycle, from study start-up through close-out, and is responsible for the timely execution of study activities and deliverables in ...

Ardelyx

Clinical Trial Associate

Newark, CA · On-site

$86K - $105K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

The CTA contributes across all phases of the clinical trial lifecycle, from study start-up through close-out, and is responsible for the timely execution of study activities and deliverables in ...

Ardelyx

Clinical Trial Associate

Newark, CA · On-site

$86K - $105K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

The CTA contributes across all phases of the clinical trial lifecycle, from study start-up through close-out, and is responsible for the timely execution of study activities and deliverables in ...

Ardelyx

Clinical Trial Associate

Newark, CA · On-site

$86K - $105K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

The CTA contributes across all phases of the clinical trial lifecycle, from study start-up through close-out, and is responsible for the timely execution of study activities and deliverables in ...

Candel Therapeutics

Clinical Trial Associate

Needham, MA · On-site

$88K - $100K/yr

The Clinical Trial Associate (CTA) role supports clinical trial execution in Ph 2 and Ph 3 trials. This role includes working on multiple protocols with the potential to cross-train across different ...

Ardelyx

Clinical Trial Associate

Newark, CA · On-site

$86K - $105K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

The CTA contributes across all phases of the clinical trial lifecycle, from study start-up through close-out, and is responsible for the timely execution of study activities and deliverables in ...

Candel Therapeutics

Clinical Trial Associate

Needham, MA · On-site

$88K - $100K/yr

The Clinical Trial Associate (CTA) role supports clinical trial execution in Ph 2 and Ph 3 trials. This role includes working on multiple protocols with the potential to cross-train across different ...

Summit Therapeutics

Clinical Trial Associate

Palo Alto, CA · On-site

$39.50 - $53.75/hr

The Senior Clinical Trial Associate (Senior CTA) is an experienced clinical operations professional who is responsible for supporting the daily workflow of clinical operations activities. They will ...

PTC Therapeutics

Clinical Trial Associate I

Warren, NJ · On-site

$34.75 - $47.50/hr

  • Medical

  • Dental

  • Vision

  • Retirement

The CTA provides essential administrative, documentation, and coordination support across all phases of clinical trial management. Working under Clinical Trial Managers (Lead CTMs and/or CTMs), the ...

Ptc Therapeutics, Inc.

Clinical Trial Associate I

Warren, NJ · On-site

$34.75 - $47.50/hr

  • Medical

  • Dental

  • Vision

  • Retirement

The CTA provides essential administrative, documentation, and coordination support across all phases of clinical trial management. Working under Clinical Trial Managers (Lead CTMs and/or CTMs), the ...

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Clinical Trial Associate Cta information

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How much do clinical trial associate cta jobs pay per hour?

As of Aug 19, 2026, the average hourly pay for clinical trial associate cta in the United States is $39.99, according to ZipRecruiter salary data. Most workers in this role earn between $32.21 and $43.99 per hour, depending on experience, location, and employer.

What does a clinical trial associate (CTA) do?

A Clinical Trial Associate (CTA) is responsible for supporting the planning, coordination, and administration of clinical trials. They help ensure that studies are conducted in compliance with regulatory guidelines and company policies. Their duties often include maintaining trial documentation, assisting with site management, and facilitating communication between clinical research teams. CTAs play a crucial role in ensuring the smooth operation of clinical studies and the accurate collection of data.

What are the key skills and qualifications needed to thrive as a clinical trial associate (CTA)?

To thrive as a Clinical Trial Associate, you need a solid understanding of clinical research processes, regulatory guidelines, and often a bachelor’s degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and GCP certification are typically required. Strong organizational skills, attention to detail, and effective communication make a CTA stand out in managing trial documentation and collaborating with cross-functional teams. These skills and qualifications are essential to ensure compliance, data integrity, and the smooth execution of clinical trials.

What are some common challenges clinical trial associates (CTAs) face when managing study documentation, and how can they be addressed?

Clinical Trial Associates often encounter challenges in maintaining accurate and up-to-date study documentation due to frequent protocol amendments, tight deadlines, and coordinating with multiple stakeholders. To address these challenges, CTAs can utilize electronic trial master file (eTMF) systems for efficient document tracking, establish clear communication channels with their team, and develop strong organizational habits. Regular training on regulatory requirements and proactive planning can also help ensure compliance and minimize errors.

What is the difference between Clinical Trial Associate Cta vs Clinical Research Coordinator CRC?

AspectClinical Trial Associate CtaClinical Research Coordinator CRC
CredentialsBachelor's degree, often certifications like ACRP or SOCRABachelor's degree, often certifications like ACRP or SOCRA
Work EnvironmentPharmaceutical companies, CROs, clinical trial sitesHospital, academic medical centers, clinical trial sites
Job FocusSupporting trial setup, monitoring, data collectionManaging daily trial operations, patient recruitment, site coordination
Industry UsageCommon in industry-sponsored trialsCommon in academic and hospital-based trials

The Clinical Trial Associate Cta primarily supports clinical trials through monitoring and data management, often working for sponsors or CROs. In contrast, the Clinical Research Coordinator CRC manages daily trial activities at clinical sites, focusing on patient recruitment and compliance. Both roles require similar credentials and work environments but differ in their specific responsibilities within the trial process.

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Clinical Trial Associate Cta jobs near you
Infographic showing various Clinical Trial Associate Cta job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 68% Full Time, 29% Part Time, 1% Temporary, and 1% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $83,169 per year, or $40 per hour.

Clinical Trial Associate

Cellectis

Manhattan, NY

$36.75 - $50.25/hr

Full-time

Re-posted 24 days ago

Job description

The Clinical Trial Associate (CTA) supports clinical study teams in the execution and oversight of clinical trials under the direction of the Vice President, Development Operations, with day-to-day guidance from the assigned Study Lead. The CTA plays a key role in study start-up, ongoing trial execution, and close-out activities, with a primary focus on document management, trial tracking, and operational support.

This role contributes to the maintenance of inspection-ready trial documentation and systems, including the Trial Master File (TMF/eTMF) and Clinical Trial Management System (CTMS), in compliance with applicable regulatory requirements (GCP/ICH), internal SOPs, and company standards.

All activities are conducted in accordance with company policies, SOPs, and corporate values.

POSITION RESPONSIBILITIES

Clinical Trial Support

  • Support study start-up activities, including site feasibility, investigator onboarding, and collection of regulatory and essential documents
  • Assist with site management activities throughout the trial lifecycle, from start-up through close-out
  • Communicate with clinical sites and vendors, as appropriate, to support timely collection of required documentation
  • Support investigational product tracking activities, including inventory documentation, shipment tracking, and reconciliation

Trial Documentation & Systems

  • Maintain accurate, complete, and inspection-ready Trial Master Files (electronic or paper)
  • Support ongoing maintenance of the Clinical Trial Management System (CTMS), ensuring data accuracy and timeliness
  • Review, file, and track clinical trial documentation in accordance with SOPs and regulatory requirements
  • Assist with quality control (QC) checks of study, country, and site-level documentation and support issue resolution

Study Tracking & Reporting

  • Maintain study trackers (e.g., regulatory submissions, site start-up timelines, protocol issue logs)
  • Track study progress and generate routine status reports and metrics as requested
  • Assist with review of monitoring visit reports (initiation, routine monitoring, and close-out)

Meetings & Cross-Functional Collaboration

  • Coordinate and support internal and external study meetings, including preparation of agendas, meeting minutes, and action item tracking
  • Collaborate with cross-functional teams, CROs, and vendors to support routine study operations
  • Provide general administrative and operational support to Development Operations team as needed

Compliance & Inspections

  • Support preparation for and follow-up on audits and regulatory inspections, as applicable
  • Assist with review of informed consent documents, case report forms, and other study-related materials

EDUCATION AND EXPERIENCE

  • Bachelor's degree (BS/BA) or equivalent preferred
  • Minimum of 1-3 years of experience supporting clinical trials, preferably in a pharmaceutical, biotechnology, or CRO environment

TECHNICAL SKILLS & CORE COMPETENCIES

  • Foundational knowledge of FDA and/or EMA regulations, ICH guidelines, and GCP requirements
  • Basic understanding of clinical trial documentation, filing structures, and operational workflows
  • Working knowledge of clinical systems such as eTMF, CTMS, and EDC platforms
  • Ability to manage multiple tasks and priorities in a fast-paced clinical development environment
  • Strong attention to detail and organizational skills
  • Proficiency in Microsoft Office applications (Word, Excel, PowerPoint)
  • Effective written, verbal, and interpersonal communication skills
  • Ability to work collaboratively across functions with appropriate supervision and guidance

Proposed Compensation Range: 80,000 - 90,000

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