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Clinical Trial Associate Cta Jobs (NOW HIRING)

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 ...

Prometrika LLC

Clinical Trial Associate II

Cambridge, MA · On-site

$75K - $90K/yr

The CTA II will: * With minimal oversight, manage all study start up, maintenance and closeout site management responsibilities, under the supervision of the Clinical Trial Manager * Lead the ...

Axsome Therapeutics

Clinical Trial Associate

New York, NY · On-site

$60K - $66K/yr

About This Role Axsome Therapeutics is seeking a Clinical Trial Associate (CTA) that is responsible for supporting the organization to successfully develop and implement clinical trials across its ...

Deciphera Pharmaceuticals

Clinical Trial Associate

Waltham, MA · On-site

$90K - $124K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

Company Description We are seeking a motivated and detail-oriented Clinical Trial Associate (CTA) to support the execution of clinical studies within our Clinical Operations team. In this role, you ...

Dyne Therapeutics

Senior Clinical Trial Associate

Waltham, MA · On-site

$36.25 - $49.25/hr

The Senior Clinical Trial Associate (CTA) is a key member of the Clinical Operations team responsible for supporting the successful planning, execution, oversight, and closeout of Dyne's global ...

Olema Oncology

Senior Clinical Trial Associate

Boston, MA · On-site

$110K - $115K/yr

Senior CTA requires 2 years' experience working as a Clinical Trial Associate. * Proficiency with Microsoft applications (e.g., Microsoft Word, Excel, PowerPoint, Outlook) * Experience with leading ...

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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 I

PTC Therapeutics

Warren, NJ • On-site

$34.75 - $47.50/hr

Full-time

Medical, Dental, Vision, Retirement

Posted 12 days ago

Job description

PTC Therapeutics is a global commercial biopharmaceutical company. For over 25 years our team has been deeply committed to a unified purpose: Extending life's moments for children and adults living with a rare disease.
At PTC, we cultivate an inclusive culture where everyone feels valued, respected, and empowered. We welcome candidates from all backgrounds to join our team, fostering a strong sense of belonging.
Visit our website to learn more about our company and culture!
Site: www.ptcbio.com
Job Description Summary:
The Clinical Trial Associate I (CTA) is a key support role within the Clinical Operations department, contributing to the execution of clinical trials that advance innovative therapies for patients with rare and serious diseases. 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 CTA ensures that trial documentation is accurate, complete, and compliance, and that study activities are well-organized and efficiently executed in alignment with regulatory guidelines and PTC's quality standards. with activities related to: study start-up; investigator site feasibility and selection; essential document review related to investigator site initiation and investigational product release and patient enrollment. This position may also provide support in project team meetings by capturing meeting minutes/action items and following up with action item owners to ensure tasks are completed.
The incumbent works cross-functionally with internal departments and external resources on clinical study related issues.
The Clinical Trial Associate I supports adherence to relevant regulatory requirements and company Standard Operating Procedures (SOPs) as appropriate.
Job Description:
ESSENTIAL FUNCTIONS
Primary duties/responsibilities:
  • Assists in the collection, review, and tracking of essential regulatory and clinical trial documents throughout the lifecycle of the study.
  • Supports the set-up, organization, and maintenance of the Trial Master File (TMF), ensuring ongoing inspection readiness and compliance with ICH-GCP and internal SOPs.
  • Helps coordinate clinical trial start-up, maintenance and close out activities, including the preparation of study materials, meeting logistics, and distribution of study communication.
  • Assists in the development and management of study trackers, tools, and logs (e.g., site contact lists, enrollment logs, action items trackers).
  • Schedules and supports internal and external study meetings, including investigator meetings, vendor calls, and cross-functional team discussions; prepares agendas and meeting minutes as needed.
  • Interfaces with Clinical Research Organizations, vendors, and clinical sites to support study related tasks and documentation collection.
  • Participants in review of monitoring reports and site-level documents such as informed consent forms and training logs.
  • Supports TMF quality control and audit preparation activities.
  • Assists in maintaining clinical trial management systems (e.g., CTMS), ensuring timely updates and accuracy of study status and documentation.
  • Facilitates and supports study-level contracting and procurement workflows in partnership with Legal and Finance, leveraging enterprise systems.
  • Collaborates with cross-functional teams (e.g., Regulatory, Data Management5, Clinical Supplies) to support ongoing study operations.
  • Participates in onsite co-monitoring and monitoring oversight visits with CTM.
  • Performs other tasks and assignments as needed and specified by management.

KNOWLEDGE/SKILLS/ABILITIES REQUIRED
* Minimum level of education and years of relevant work experience.
  • Bachelor's degree in a relevant life science or healthcare-related discipline and minimum 2 years of clinical research support experience in a pharmaceutical, biotechnology, or related environment or a recognized equivalent of education and experience.

* Special knowledge or skills needed and/or licenses or certificates required.
  • Familiarity with clinical trial study documents.
  • Knowledge of Good Clinical Practice (GCP) and International Conference on Harmonisation (ICH) guidelines.
  • Proficiency with Microsoft Office Suite (Word, Excel, PowerPoint).
  • Excellent verbal and written communication skills.
  • Ability to work independently and collaboratively, as required, in a fast-paced, matrixed, team environment consisting of internal and external team members.
  • Analytical thinker with excellent problem-solving skills and the ability to adapt to changing priorities and deadlines.
  • Excellent planning, organization and time management skills including the ability to support and prioritize multiple projects.

*Special knowledge or skills and/or licenses or certificates preferred.
  • Experience with TMFs. Performing periodic ad hoc, interim and end-of-study reviews/audits on paper and electronic TMFs for several trials to ensure TMF meets sponsor's expectations (includes TMF reconciliation at study close-out)

* Travel requirements
  • 10-15%

Expected Base Salary Range
$81,900 - $103,100. The base salary offered will be contingent on assessment of candidate education level, background, and experience relative to the requirements of the position they are being considered for, as well as review of internal equity.
In addition to base salary, PTC employees are also eligible for short- and long-term incentives. All eligible employees may also enroll in PTC's medical, dental, vision, and retirement savings plans.
#LI-NM1
EEO Statement:
PTC Therapeutics is an equal opportunity employer. We welcome applications from all individuals, regardless of race, color, national origin, gender, age, physical characteristics, social origin, disability, religion, family status, pregnancy, sexual orientation, gender identity, gender expression, disability, veteran status or any unlawful criterion under applicable law. We are committed to treating all applicants fairly and avoiding discrimination.
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