ZipRecruiter

Log In

1

Clinical Trial Associate Cta Jobs (NOW HIRING)

Doist

Sr. Clinical Trial Associate

Princeton, NJ · On-site

$117 - $137/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 ...

New

Doist

Sr. Clinical Trial Associate

Miami, FL · On-site

$117 - $137/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 ...

New

Olema Oncology

Senior Clinical Trial Associate

Boston, MA · On-site

$36.50 - $49.75/hr

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 ...

Prometrika LLC

Clinical Trial Manager

Cambridge, MA · On-site

$140K - $168K/yr

Manage Clinical Trial Associates (CTA) and other study staff, as needed * Recommend and implement innovative process ideas to impact clinical trials management * Organize and manage internal team ...

Verastem Oncology

Clinical Trial Associate

Boston, MA · On-site

$86 - $100/hr

Summary Responsible for assisting and providing support to the members of the clinical operations project team to facilitate the operational execution of the clinical trial processes in accordance ...

Verastem

Clinical Trial Associate

Boston, MA · On-site

$86K - $100K/yr

Responsible for assisting and providing support to the members of the clinical operations project team to facilitate the operational execution of the clinical trial processes in accordance with ...

Rapport Therapeutics

Sr. Clinical Trial Associate

Boston, MA · On-site

$36.25 - $49.50/hr

As a Senior Clinical Trial Associate, you'll be a key player in keeping our Bipolar Mania studies on track-managing the details, supporting the team, and helping bring innovative treatments to ...

previous page

Showing results 41-60

All JobsHealthcare JobsMedical Research JobsClinical Laboratory Technician JobsClinical Trial Associate Cta Jobs

Clinical Trial Associate Cta information

See salary details

$17

$39

$70

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.

More about Clinical Trial Associate Cta jobs

What cities are hiring for Clinical Trial Associate Cta jobs?

Cities with the most Clinical Trial Associate Cta job openings:

What are the most commonly searched types of Clinical Trial Cta jobs?

The most popular types of Clinical Trial Cta jobs are:

What states have the most Clinical Trial Associate Cta jobs?

States with the most job openings for Clinical Trial Associate Cta jobs include:

What job categories do people searching Clinical Trial Associate Cta jobs look for?

The top searched job categories for Clinical Trial Associate Cta jobs are:

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.

Sr. Clinical Trial Associate

Deciphera Pharmaceuticals

Waltham, MA • On-site

$115K - $159K/yr

Full-time

Medical, Dental, Vision, Retirement

Re-posted 19 days ago

Job description

Company Description
Job Description
We are seeking a detail-oriented and proactive Sr. Clinical Trial Associate (Sr. CTA) to support the successful execution of clinical studies within Clinical Operations. In this role, you will partner closely with study leads and cross-functional teams to manage key components of clinical trials, ensuring delivery against timelines, budgets, and quality standards.
This is an excellent opportunity for a clinical operations professional who thrives in a fast-paced environment and is eager to contribute to high-impact clinical programs.
Study Team & Meeting Management
  • Coordinate cross-functional study team meetings, including agenda development and meeting minutes
  • Support clinical site start-up activities and ongoing site management efforts
  • Assist in managing external vendors and ensure alignment with study expectations
  • Participate in, and occasionally present at, Investigator Meetings

Study Documentation, Tracking & Execution
  • Maintain and track study documentation to ensure compliance with internal standards and regulatory requirements
  • Support Trial Master File (TMF) management, including document filing and quality control
  • Assist with development, editing, and distribution of key study documents (e.g., informed consent forms, manuals)
  • Maintain study trackers, tools, and systems to support study execution

Study Planning & Quality Oversight
  • Analyze clinical systems and processes to identify risks to data quality and integrity
  • Provide input into protocol feasibility and identify opportunities to optimize study delivery
  • Develop and manage study timelines, proactively identifying risks and escalating issues as needed
  • Support clinical trial budgeting activities and cost tracking
  • Track regulatory documents (e.g., 1572s) and collaborate with Regulatory on submissions such as INDs
  • Support sample management and contribute to review of core study documents as applicable

Qualifications
Required Qualifications
  • Bachelor's or Master's degree with at least 3 years of clinical operations experience in a pharmaceutical company and/or CRO
  • Solid understanding of ICH guidelines, GCP, and key regulatory requirements
  • Ability to independently manage assigned components of clinical trials with minimal oversight
  • Strong attention to detail and organizational skills

Preferred Experience & Skills
  • Experience working with clinical trial systems and vendor platforms
  • Understanding of data, technology, and vendor interdependencies across clinical studies
  • Strong verbal, written, and presentation skills
  • Ability to problem-solve, prioritize, and manage multiple activities simultaneously

Additional Information
Deciphera is committed to fair and equitable compensation practices. The base salary pay range for this role is $115,000 - $159,000. Actual compensation packages will depend on various factors, including, but not limited to depth of experience, education, skillset, overall performance and/or location.
Deciphera believes in providing a competitive compensation and benefits package to all employees. Our base salary is just one component of Deciphera's competitive total rewards strategy that also includes annual performance bonus, a long-term incentive plan, full range of benefits and other incentive compensation plans (if applicable)
Benefits:
  • Competitive salary and annual bonus.
  • Comprehensive benefits package including medical, dental, vision insurance, 401(k) retirement plan with company match, and more.
  • Generous parental leave and family planning benefits.
  • Outstanding culture and opportunities for personal and professional growth.

EQUAL EMPLOYMENT OPPORTUNITY INFORMATION
Deciphera is committed to equal employment opportunity and values diversity. To ensure that we comply with reporting requirements, we invite you complete the confidential survey at the end of this application. Providing this information is optional. It will not be accessible or used in the hiring process, and has no effect on your opportunity for employment. This information will also be treated confidentially. We are committed to make all hiring decisions and other employment decisions on a non-discriminatory basis.

Apply