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Clinical Trial Operations Jobs in Virginia (NOW HIRING)

Cardiology Physician

Norfolk, VA ยท On-site

$345K - $390K/yr

Expansion of system-wide clinical trial operations Benefits: * Flexible RVU structure to ensure adequate administrative and research time * Highly competitive salary * Academic appointments through ...

$502K - $650K/yr

Mentor practitioners in clinical trial development and encourage physician, APP, pharmacist, and ... operational oversight. The alliance will establish a Joint Clinical Trials Program Steering ...

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Clinical Trial Operations information

See Virginia salary details

$17

$39

$69

How much do clinical trial operations jobs pay per hour?

As of Sep 7, 2026, the average hourly pay for clinical trial operations in Virginia is $39.64, according to ZipRecruiter salary data. Most workers in this role earn between $31.92 and $43.61 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.

What are the most commonly searched types of Clinical Trial Operations jobs in Virginia?

The most popular types of Clinical Trial Operations jobs in Virginia are:

Infographic showing various Clinical Trial Operations job openings in Virginia as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 18% Part Time, 1% Temporary, 2% Contract, and 1% Nights. Highlights an 93% Physical, 3% Hybrid, and 4% Remote job distribution, with an average salary of $82,456 per year, or $39.6 per hour.

Clinical Trial & Pharmacovigilance Manager

VENESCO LLC

Falls Church, VA โ€ข On-site

Full-time

Re-posted 27 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