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Clinical Trial Operations Jobs (NOW HIRING)

Candel Therapeutics

Clinical Trial Associate

Needham, MA · On-site

$88K - $100K/yr

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 ...

ICON

Clinical Trial Manager

Center Square, PA · On-site

$120 - $180/hr

Clinical Operations Lead ICON plc is a world-leading healthcare intelligence and clinical research ... As a Clinical Trial Manager at ICON, you will manage clinical trial operations activities ...

New

Clinovo

Clinical Trial Manager

Cambridge, MA · On-site

$175K/yr

The Clinical Trial Manager (CTM) plays a key role in the successful execution of clinical research studies, providing operational leadership from study initiation through final closeout. This ...

Legend Biotech USA, Inc.

$35.50 - $48.25/hr

Legend Biotech is seeking a Senior Clinical Trial Associate as part of the Clinical Operations team basedin Somerset, NJ.Location: RemoteRole OverviewWe are seeking a highly skilled and motivated ...

Kardigan

Clinical Trial Manager

Princeton, NJ · On-site

As a Clinical Trial Manager (CTM), you will be part of the Clinical Operations team reporting to the asset's Clinical Trial or Clinical Program Lead. This position will be responsible for the ...

SAB

Clinical Sample Manager

Sioux Falls, SD · Remote

$130K - $150K/yr

Provide operational oversight of assigned clinical trial service providers, ensuring services are delivered according to study requirements, quality standards, and timelines. * Serve as the primary ...

SAB

Clinical Trial Manager, Immunology

Miami Beach, FL · On-site

$120 - $180/hr

Manage all aspects of clinical trial operations, ensuring adherence to timelines, budgets, and regulatory requirements. * Participate in the identification, evaluation, selection, and oversight of ...

SAB

Clinical Trial Manager, Immunology

Tulsa, OK · On-site

$90 - $140/hr

Manage all aspects of clinical trial operations, ensuring adherence to timelines, budgets, and regulatory requirements. * Participate in the identification, evaluation, selection, and oversight of ...

SanegeneBio Inc.

PM, Clinical Operation

China, TX · On-site

$120 - $190/hr

Qualifications * Background in biochemistry, medicine, or related life science disciplines, with more than 6 years of clinical trial operations and project management experience. * Strong ...

Vanguard Clinical

Clinical Operations Associate (Pool)

CA · Remote

$70K - $80K/yr

We are experts in clinical trial operations with a focus on Clinical Trial Management, CRO/Vendor Oversight, Trial Master File Management, Clinical Monitoring, Quality Assurance, Data Management and ...

SAB

Clinical Trial Manager, Immunology

Miami Beach, FL · Remote

$150K - $165K/yr

Manage all aspects of clinical trial operations, ensuring adherence to timelines, budgets, and regulatory requirements. * Participate in the identification, evaluation, selection, and oversight of ...

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Clinical Trial Operations information

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How much do clinical trial operations jobs pay per hour?

As of Sep 7, 2026, the average hourly pay for clinical trial operations 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 clinical trial operations?

A Clinical Trial Operations job involves overseeing the planning, execution, and management of clinical trials to ensure they comply with regulatory guidelines and study protocols. Professionals in this role coordinate with investigators, sponsors, and regulatory agencies to ensure trials run smoothly and efficiently. They manage timelines, budgets, patient recruitment, data collection, and compliance with ethical and legal standards. Their ultimate goal is to ensure the trial produces reliable data while prioritizing patient safety.

What are the typical daily responsibilities in clinical trial operations?

A clinical trial operations professional oversees the planning, implementation, and management of clinical research studies. Daily tasks often include coordinating study timelines, monitoring site performance, ensuring adherence to regulatory requirements, managing study documentation, and communicating with trial sites and sponsors. The role also involves addressing operational issues quickly and adjusting plans as needed to keep the trial on track. This position usually works closely with principal investigators, data managers, regulatory teams, and sponsors, making collaboration and communication essential for success.

What are the key skills and qualifications needed to thrive in clinical trial operations?

To thrive in Clinical Trial Operations, you typically need a background in life sciences or healthcare, strong project management abilities, and familiarity with clinical research protocols and regulatory guidelines. Experience with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and certifications like GCP (Good Clinical Practice) are often required. Excellent organizational, communication, and problem-solving skills help you collaborate effectively with cross-functional teams and manage complex study logistics. These competencies are crucial to ensuring clinical trials run smoothly, efficiently, and in compliance with industry standards.

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Clinical Trial Operations jobs near you
Infographic showing various Clinical Trial Operations job openings in the United States as of August 2026, with employment types broken down into 84% Full Time, 13% Part Time, 1% Temporary, 1% Contract, and 1% Nights. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $83,169 per year, or $40 per hour.

Clinical Trial Associate

Candel Therapeutics

Needham, MA • On-site

$88K - $100K/yr

Full-time

Re-posted 24 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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