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Clinical Trial Study Assistant Jobs (NOW HIRING)

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 ... * Assist in collecting and completing essential study-related activities, including data entry ...

Ardelyx

Clinical Trial Associate

Newark, CA · On-site

$86K - $105K/yr

Provide operational support for assigned clinical trial(s) across all phases of the study lifecycle, including start‑up, conduct and close‑out activities. * Assist Clinical Trial Managers (CTMs ...

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 ... * Assist in collecting and completing essential study-related activities, including data entry ...

Kardigan

Clinical Trial Manager

Princeton, NJ · Remote

Kardigan is seeking a Clinical Trial Manager to contribute to the planning, oversight and delivery of its cardiovascular clinical studies. As a Clinical Trial Manager (CTM), you will be part of the ...

Ardelyx

Clinical Trial Associate

Newark, CA · On-site

$86K - $105K/yr

Provide operational support for assigned clinical trial(s) across all phases of the study lifecycle, including start-up, conduct and close-out activities * Assist Clinical Trial Managers (CTMs) and ...

Frontier Medicines

Clinical Trial Manager

Boston, MA · Hybrid

$120K - $150K/yr

... Assist with oversight of CRO and vendor set-up, liaising with CROs to ensure timely study ... Coordinate Clinical Trial Team meetings and drive action item follow-up. Maintain clinical ...

Ardelyx

Clinical Trial Associate

Newark, CA · On-site

$86K - $105K/yr

Provide operational support for assigned clinical trial(s) across all phases of the study lifecycle, including start-up, conduct and close-out activities * Assist Clinical Trial Managers (CTMs) and ...

Ardelyx

Clinical Trial Associate

Newark, CA · On-site

$86K - $105K/yr

Provide operational support for assigned clinical trial(s) across all phases of the study lifecycle, including start-up, conduct and close-out activities * Assist Clinical Trial Managers (CTMs) and ...

Clinovo

Clinical Trial Manager

Waltham, MA · On-site

The Role The Clinical Trial Manager (CTM) will be a key contributor to the successful execution of ... The CTM will work closely with cross-functional study teams to ensure assigned clinical trials are ...

Ardelyx

Clinical Trial Associate

Newark, CA

$86K - $105K/yr

Provide operational support for assigned clinical trial(s) across all phases of the study lifecycle, including start-up, conduct and close-out activities * Assist Clinical Trial Managers (CTMs) and ...

Ardelyx

Clinical Trial Associate

Newark, CA · On-site

Provide operational support for assigned clinical trial(s) across all phases of the study lifecycle, including start-up, conduct and close-out activities * Assist Clinical Trial Managers (CTMs) and ...

Aerogen Ltd

Clinical Trial Manager

Morrisville, NC · On-site

... • Assist in the development of study documents and tools including informed consent forms ... clinical trial applications, protocols, protocol amendments, clinical study reports and ...

Lyell Immunopharma

Clinical Trial Assistant

Seattle, WA · On-site

Supports drafting of study plans, process documents and creates forms as needed for efficient trial execution; collaborates and seeks feedback from broader study team stakeholders to improve/optimize ...

Legend Biotech US

Senior Clinical Trial Associate

Somerset, NJ · Hybrid

$35.50 - $48.25/hr

... study correspondence. * Ensure documentation is current, complete, and compliant with ICH-GCP and company SOPs. * Assist with the planning, start-up, execution, and close-out of clinical trials ...

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Clinical Trial Study Assistant information

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How much do clinical trial study assistant jobs pay per hour?

As of Sep 12, 2026, the average hourly pay for clinical trial study assistant in the United States is $37.67, according to ZipRecruiter salary data. Most workers in this role earn between $25.72 and $48.08 per hour, depending on experience, location, and employer.

What cities are hiring for Clinical Trial Study Assistant jobs?

Cities with the most Clinical Trial Study Assistant job openings:

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Infographic showing various Clinical Trial Study Assistant job openings in the United States as of July 2026, with employment types broken down into 3% As Needed, 74% Full Time, 18% Part Time, and 5% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $78,347 per year, or $37.7 per hour.

Clinical Trial Associate

Needham, MA • On-site

Candel Therapeutics
Biotechnology Research and Development • 51 - 200 employees
Learn more about Candel Therapeuticsexternal

$88K - $100K/yr

Full-time

Re-posted 29 days ago

Job description

  • Location:Hybrid, Needham, MA
  • Salary: $88k-$100k

Why Work With Us?
At Candel, our people drive our success. We value diversity, collaboration, and bold thinking in a supportive, mission-driven environment. Like a team, we show up for each other and stay focused on making a difference for patients and families. Our leadership is transparent and empowering, and our culture is built on trust, flexibility, and accountability, encouraging ownership and innovation every day.
Our Science: Advancing Cancer Immunotherapies
Candel is a clinical-stage biopharma company developing off-the-shelf, multimodal immunotherapies that stimulate personalized, systemic anti-tumor responses. Our platforms use genetically modified adenovirus and HSV constructs. With positive Phase 3 results for our lead candidate, it's an exciting time to join us and help bring transformative cancer treatments to patients. Learn more:www.candeltx.com
Position Summary:
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 oncology indications using a variety of clinical trial databases.
Essential Areas of Responsibility:
  • Execute and support day-to-day clinical trial operations in alignment with protocols, timelines, and regulatory requirements.
  • Participate in reviewing, formatting, and finalizing study-related templates, logs, plans, and manuals and ongoing training of personnel.
  • Assist in collecting and completing essential study-related activities, including data entry into multiple databases.
  • Ensure the quality of data submitted from assigned study tasks and timely data submission, including appropriate progress reporting.
  • Manage imaging vendor and maintain tracking of invoices, sample delivery and recovery from the vendor site.
  • Assist in the planning and organizing study-specific meetings and write and distribute regular updates.
  • Assist the Clinical Trial Manager in select site management activities. This could include a review of monitoring reports and source document review.
  • Maintain study-related trackers that will support Clinical Operations and individual studies.
  • Perform primary review of submitted clinical data, database entry, and source document verification according to established standard operating procedures (SOPs).
  • participate in the review and verification of data for quality control processes.
  • Ensure quality in documentation and archiving of clinical data.
  • Support invoice tracking, purchase order coordination, and budget-related activities for study.

Minimum Education, Experience and Skill Requirements:
Education:
  • Bachelor's degree in a health-related discipline or similar.

Experience:
  • At least 2 years of experience in the clinical research/pharmaceutical/biotech arena and an understanding of clinical research and the requirements of a clinical operations function.
  • Excellent verbal and written communication skills, good organizational and interpersonal skills, and team drive.
  • Knowledge of GCP and FDA regulations related to clinical trial conduct and familiarity with industry best practices.
  • Able to manage multiple projects independently and use varying databases and management systems.
  • Discretion in handling confidential information.
  • Knowledge of project management tools and practices and proficiency in using normal office software: Microsoft Word, Excel, and PowerPoint.

Must be authorized to work in US. We cannot provide sponsorships.
*** NOTE: We are not accepting resumes from agencies. ***

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