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Sr Clinical Trial Associate Jobs (NOW HIRING)

Predicine, Inc

Clinical Trial Associate

Hayward, CA · On-site

$38.50 - $52.50/hr

Clinical Trial Associate Location: Onsite, Hayward, CA Department: Clinical Development Employment Type: Full Time Position Overview: The Clinical Trial Associate reports to Associate Director ...

Ardelyx

Clinical Trial Associate

Newark, CA · On-site

$86K - $105K/yr

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

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 ...

ICON

Clinical Trial Associate

Blue Bell, PA · On-site

$32 - $43.75/hr

Clinical Trial Associate ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven ...

Ardelyx

Clinical Trial Associate

Newark, CA · On-site

$86 - $105/hr

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

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 ...

Ardelyx

Clinical Trial Associate

Newark, CA

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

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

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 ...

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 ...

Candel Therapeutics

Clinical Trial Associate

Needham, MA · On-site

$88 - $100/hr

Learn more: www.candeltx.com Position Summary The Clinical Trial Associate (CTA) role supports clinical trial execution in Phase 2 and Phase 3 trials. This role includes working on multiple protocols ...

Actalent

Clinical Trial Associate - Hybrid

Bala Cynwyd, PA · Hybrid

$31.50 - $43/hr

Clinical Trial Associate The Clinical Trial Associate (CTA) supports the Director of Clinical Operations and Clinical Study Managers in trial start-up, execution, and close-out activities while ...

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Sr Clinical Trial Associate information

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

As of Sep 6, 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 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.

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 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.

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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 1% As Needed, 70% Full Time, 27% 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/Senior Clinical Trial Associate

Crescent Biopharma

Waltham, MA • On-site

$110 - $150/hr

Other

Re-posted 8 days ago

Job description

Crescent Biopharma’s vision is to build a world leading oncology company bringing the next wave of therapies for cancer patients. The Company’s clinical-stage pipeline includes its lead program, a PD-1 x VEGF bispecific antibody, as well as novel antibody-drug conjugates. By leveraging multiple modalities and established targets, Crescent aims to rapidly advance potentially transformative therapiesas single agentsand as part of combination regimens to treat a range of solid tumors. For more information, visit www.crescentbiopharma.com and follow the Company on LinkedIn and X.

We are seeking a CTA/Senior CTA who will work with the Clinical Study Lead and Director of Clinical Operations to support the conduct of clinical trials. You will partner with the Clinical Study Lead to ensure studies are completed on time, within budget, and in compliance with SOPs, FDA regulations and ICH/GCP guidelines.

You may independently manage components of clinical studies, including but not limited to vendor oversight, budgets, responsibility for a subset of sites or countries, or phases of the trial (startup period, for example), with oversight.

Responsibilities
  • Support the Clinical Study Lead and Clinical Operations team in the day-to-day operational activities of clinical trials to ensure study objectives, timelines, quality standards, and regulatory requirements are met.
  • Support oversight of CROs, vendors, and investigator sites, including review of monitoring visit reports, site communications, and follow-up on study-related actions and issues.
  • Maintain study tracking tools for key study documentation (e.g., Form FDA 1572) and operational activities, including site activation, enrollment, monitoring visit status, IRB/EC approvals, safety letter distribution, training compliance, and study milestones.
  • Support Trial Master File (eTMF) activities, including document collection, filing, reconciliation, quality control reviews, and inspection readiness efforts.
  • Support preparation of study agendas, meeting minutes, action item logs, and study status reports while ensuring effective communication across internal teams, CROs, vendors, and investigator sites.
  • Collaborate cross-functionally with Regulatory Affairs, Clinical Supplies, Data Management, Safety, Quality, and other functional areas to support study deliverables and timelines.
  • Manage study team training records and ensure compliance with applicable SOPs, regulations, study requirements, and company policies.
  • Manage system access requests for study team and site personnel, as needed.
  • Communicate and elevate study risks, protocol deviations, operational challenges, and other study-related issues as appropriate.
Education & Experience
  • Bachelor’s degree in scientific or related field with 2+ years of experience in Clinical Operations, clinical research or healthcare, or equivalent experience
  • Knowledge of FDA regulatory requirements and ICH/GCP guidelines essential
  • Demonstrated efficiency
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