ZipRecruiter

Log In

1

Sr Clinical Trial Associate 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 ...

Ardelyx

Clinical Trial Associate

Newark, CA

$86K - $105K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

The Clinical Trial Associate (CTA) supports the Clinical Trial Management team in the execution of ... and other senior team members with day-to-day study activities to ensure study milestones and ...

Ardelyx

Clinical Trial Associate

Newark, CA · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

The Clinical Trial Associate (CTA) supports the Clinical Trial Management team in the execution of ... and other senior team members with day-to-day study activities to ensure study milestones and ...

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

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.

Ardelyx

Clinical Trial Associate

Newark, CA · On-site

$86K - $105K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

The Clinical Trial Associate (CTA) supports the Clinical Trial Management team in the execution of ... and other senior team members with day-to-day study activities to ensure study milestones and ...

Ardelyx

Clinical Trial Associate

Newark, CA · On-site

$86K - $105K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

The Clinical Trial Associate (CTA) supports the Clinical Trial Management team in the execution of ... and other senior team members with day-to-day study activities to ensure study milestones and ...

Ardelyx

Clinical Trial Associate

Newark, CA

$86K - $105K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

The Clinical Trial Associate (CTA) supports the Clinical Trial Management team in the execution of ... and other senior team members with day-to-day study activities to ensure study milestones and ...

Spyglass Pharma

Clinical Trial Associate

Aliso Viejo, CA

$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.

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 ...

previous pagenext page

Showing results 21-40

All JobsSr Clinical Trial Associate Jobs

Sr Clinical Trial Associate information

See salary details

$17

$39

$70

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

As of Aug 16, 2026, the average hourly pay for sr clinical trial associate 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 is the difference between Sr Clinical Trial Associate vs Clinical Trial Associate?

AspectSr Clinical Trial AssociateClinical Trial Associate
Required CredentialsBachelor's degree, experience in clinical trials, often some certificationBachelor's degree, entry-level experience in clinical trials
Work EnvironmentPharmaceutical companies, CROs, clinical research sitesSimilar environments, often entry-level roles in the same settings
Employer & Industry UsageUsed in pharmaceutical, biotech, CROs for experienced rolesUsed across similar industries for entry-level positions
Search & Comparison IntentUnderstanding advanced responsibilities and experience levelEntry-level understanding and career progression

The main difference between a Sr Clinical Trial Associate and a Clinical Trial Associate lies in experience, responsibilities, and qualifications. The senior role typically requires more experience and involves overseeing trial activities, while the associate position is more focused on supporting trial operations. Both roles are essential in clinical research, but the senior associate has a broader scope and leadership responsibilities.

What are the key skills and qualifications needed to thrive as a Sr Clinical Trial Associate, and why are they important?

To thrive as a Sr Clinical Trial Associate, you need a solid understanding of clinical research processes, regulatory compliance, and usually a Bachelor's degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, CTMS platforms, and GCP certification is often required. Strong organizational skills, attention to detail, and effective communication make candidates stand out in this role. These skills are essential to ensure trials run smoothly, data integrity is maintained, and regulatory standards are met throughout the clinical study lifecycle.

What is a Sr Clinical Trial Associate?

Senior Clinical Trial Associates (Sr CTAs) are experienced professionals who support the management and coordination of clinical trials within the pharmaceutical, biotechnology, or medical device industries. They assist in planning, organizing, and overseeing clinical trial activities, ensuring compliance with regulatory requirements and study protocols. Sr CTAs often handle documentation, monitor trial progress, liaise with study sites, and help resolve operational issues. Their role is vital to maintaining data quality and supporting the successful execution of clinical studies.

How does a Sr Clinical Trial Associate typically collaborate with cross-functional teams during a study?

As a Sr Clinical Trial Associate, you will regularly interact with teams such as regulatory affairs, data management, project management, and clinical research coordinators. Collaboration often involves coordinating study startup activities, tracking site progress, and ensuring smooth communication between internal teams and external vendors. You may participate in meetings to address site issues, help prepare documentation for compliance, and support the clinical project manager with oversight of study timelines. Effective teamwork and strong communication skills are essential for ensuring the success of clinical trials.
More about Sr Clinical Trial Associate jobs

What cities are hiring for Sr Clinical Trial Associate jobs?

Cities with the most Sr Clinical Trial Associate job openings:

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

The most popular types of Sr Clinical Trial jobs are:

What states have the most Sr Clinical Trial Associate jobs?

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

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

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

Sr Clinical Trial Associate jobs near you
Infographic showing various Sr Clinical Trial Associate job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 72% Full Time, 17% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $83,169 per year, or $40 per hour.

Senior Clinical Trial Associate

Treeline Biosciences

Watertown, MA

$68K - $94K/yr

Full-time

Re-posted 6 days ago

Job description

Clinical Trial Associate 

This individual will assist the clinical operations team in the day-to-day operations, study start up, execution, and closeout of trials across the portfolio.

Responsibilities

  • Support the day-to-day operations of trials to ensure completion per established project team goals and objectives in compliance with ICH/GCP guidelines, from study start-up to close-out.
  • Develop and maintain internal trial trackers and implement updates to presentations and reports based on pertinent trial information (e.g. site start up status, screening and enrollment, bioanalytical samples, clinical supplies)
  • Ensure timely maintenance of the Trial Master File (TMF) according to regulatory guidance and internal SOPs. Lead periodic TMF review and reconciliation activities throughout the lifecycle of trials. Identify issues and propose mitigations as part of CRO oversight of TMF related activities..
  • Participate in and ensure appropriate documentation of clinical team meetings, including meeting minutes, agendas, and action items.
  • Assist with planning and conduct of internal and external meetings (study meetings, study site meetings, vendor meetings, Clinical Advisory Board meetings, etc.)
  • Oversee study vendors including central labs, IRT and other service providers.
  • Manage vendor POs and trial payments (including budget reconciliation), including invoice review, approval, and tracking.
  • Support the set-up and management of clinical trial supplies and biosample management where needed (e.g., drug product, ancillary supplies).
  • Lead and coordinate development and team review of study documents including protocols, informed consent forms, and study-specific plans.
  • Assist the Clinical Trial Manager with site start-up activities, communications, and tracking
  • Assist in data reviews, tracking of data entry and query status as needed.

Education, Skills, Experience

  • Two plus years of relevant trial support experience (including CRO or vendor oversight experience).
  • BA/BS degree preferred. (Additional experience may substitute for a BA/BS degree.) Oncology experience is favorable.
  • General working knowledge of drug development and ICH/GCP guidelines and clinical trial operations is required.
  • Ability to work independently and take initiative on projects under minimal supervision.
  • Excellent organizational skills; prefers and can adapt to multiple priorities in a fast-paced and fluid work environment.
  • Excellent interpersonal, written, verbal, administrative, and computer skills.

This position is classified as exempt. The anticipated annual base salary range for candidates who will work in Watertown is $68,883 to $94,945. The final base salary offered to the successful candidate will be dependent upon several factors that may include but are not limited to the type and length of experience within the job, and other factors. Treeline Biosciences is a multi-state employer, and this salary range may not reflect positions that work in other cities or states.

 

Recruitment fraud statement

Please be aware of recruitment fraud and related job scams, where scammers present themselves as recruiters but are seeking to steal money or personal information. Keep the following in mind to protect yourself:

  • Treeline Biosciences will never ask for money from you as part of our recruitment process. Do not provide bank details or pay somebody for the promise of a job at Treeline.
  • We do not conduct interviews through RingCentral, Skype or Telegram.
  • Our job openings are first posted to treeline.bio/careers. If you locate a listing for a Treeline job on another site, please ensure it is also posted on our careers website.
  • You can find more information about job scams at consumer.ftc.gov/articles/job-scams.
  • To report job scams, head to ReportFraud.ftc.gov.

Apply