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Clinical Trial Operations Jobs (NOW HIRING)

Kardigan

Clinical Trial Manager

Princeton, NJ · Remote

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 ...

Viking Therapeutics

Clinical Trial Manager

San Diego, CA · On-site

$110K - $140K/yr

Manages trial operational plan and CRO activities, including project timelines & quality of deliverables, and managing approved trial budget(s) throughout the life of the assigned clinical trial(s)

VIKING THERAPEUTICS INC

Clinical Trial Manager

San Diego, CA · On-site

$110K - $140K/yr

Manages trial operational plan and CRO activities, including project timelines & quality of deliverables, and managing approved trial budget(s) throughout the life of the assigned clinical trial(s)

Apply Early

Careerxchange

Operations Manager Clinical Trials

Miami, FL · On-site

$41 - $56/hr

The ideal candidate has strong leadership skills, experience managing clinical trial operations, and a thorough understanding of FDA regulations, Good Clinical Practice (GCP), and clinical research ...

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Actalent

Clinical Trial Associate

Wayne, PA

$30.25 - $41.50/hr

Clinical Trial Associate The Clinical Trial Associate supports the planning, execution, and ... This role works closely with the Clinical Operations study management team to ensure efficient ...

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Clinical Trial Operations information

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How much do clinical trial operations jobs pay per hour?

As of Jul 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 are clinical trial operations?

Clinical trial operations involve managing and coordinating all activities required to conduct a clinical trial, including site selection, patient recruitment, data collection, and regulatory compliance. Professionals in this field ensure the trial progresses efficiently, often using specialized software and adhering to Good Clinical Practice (GCP) standards.

Is CRA better than CRC?

A Clinical Research Associate (CRA) and a Clinical Research Coordinator (CRC) are different roles in clinical trial operations. CRAs typically oversee multiple sites, monitor trial progress, and ensure compliance, often working remotely or traveling frequently, while CRCs manage day-to-day trial activities at a specific site, including patient recruitment and data collection. Both roles require knowledge of Good Clinical Practice (GCP) and may involve certifications like CCRP or RAC, but they focus on different aspects of trial management.

What are the key skills and qualifications needed to thrive in the Clinical Trial Operations position, and why are they important?

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.

What are the highest paying clinical trials?

Clinical Trial Operations professionals can earn higher pay when working on high-stakes or complex trials, such as those for rare diseases, oncology, or advanced therapeutics, which often have larger budgets. Additionally, roles involving seniority, specialized skills, or working for pharmaceutical companies tend to offer higher compensation. Experience, certifications, and the trial's scope influence salary levels in this field.

What is a Clinical Trial Operations job?

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 typical daily responsibilities in a Clinical Trial Operations role?

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 jobs in the US pay 300,000 a year?

In clinical trial operations, senior roles such as Clinical Trial Directors or Vice Presidents can reach or exceed a $300,000 annual salary, especially with extensive experience, leadership responsibilities, and in large pharmaceutical or biotech companies. These positions often require advanced degrees, strong project management skills, and a deep understanding of regulatory requirements.
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Clinical Trial Operations jobs near you
Clinical Trial & Pharmacovigilance Manager

Clinical Trial & Pharmacovigilance Manager

VENESCO, LLC

Falls Church, VA • Hybrid

Other

Posted 24 days ago

Job description

Description

 Clinical Trial & Pharmacovigilance Manager

Location: Hybrid
Job Type: Full-Time

Position Overview:
Venesco is seeking an experienced Clinical Trial & Pharmacovigilance Manager to oversee clinical trial operations and ensure robust safety surveillance practices.


Requirements

Key Responsibilities:   Manage clinical trial operations from startup through closeout   Oversee adverse event reporting and pharmacovigilance systems   Ensure compliance with ICH-GCP and regulatory requirements   Coordinate DSMB activities and safety reviews   Develop and maintain clinical study documentation   Collaborate with regulatory teams on submissions

Minimum Qualifications:   Advanced degree in clinical research, life sciences, or related healthcare field   8+ years of clinical operations and safety experience   Strong knowledge of ICH-GCP and FDA regulations

Preferred Qualifications:   Experience with Argus or ArisG safety databases   Clinical trial management certification MUST BE A US CITIZEN and US Board certified MD

Apply