ZipRecruiter

Log In

1

Clinical Study Manager Jobs in Virginia (NOW HIRING)

Epic Health Partners

Senior Clinical Manager

Danville, VA · On-site

$75K - $80K/yr

We are seeking a dynamic and experienced Senior Clinical Manager to provide leadership, oversight, and support across behavioral health programs. This role is responsible for strengthening clinical ...

Riverside Health System Non-Providers

$68K - $93K/yr

Gathers and records all required study related to the Clinical Trial Management System (CTMS). Reports all Serious Adverse Events (SAE) to the Principle Investigator, monitor, sponsor, and IRB as ...

Riverside

$68K - $93K/yr

Gathers and records all required study related to the Clinical Trial Management System (CTMS). Reports all Serious Adverse Events (SAE) to the Principle Investigator, monitor, sponsor, and IRB as ...

Alcanza Clinical Research

$23.50 - $31.25/hr

The Clinical Research Coordinator under the direction of the Site Manager/Director and the Principal/Sub Investigators conducts the following according to the study protocol, company processes ...

next page

Showing results 1-20

All JobsClinical Study JobsClinical Study Manager JobsClinical Study Manager Jobs in Virginia

Clinical Study Manager information

See Virginia salary details

$28

$61

$95

How much do clinical study manager jobs pay per hour?

As of Jul 26, 2026, the average hourly pay for clinical study manager in Virginia is $61.98, according to ZipRecruiter salary data. Most workers in this role earn between $50.29 and $69.81 per hour, depending on experience, location, and employer.

Is CRC an entry level position?

A Clinical Research Coordinator (CRC) is often considered an entry-level role in clinical research, requiring basic knowledge of study protocols and good clinical practice (GCP). However, some positions may prefer prior healthcare or research experience, and advancement typically involves gaining additional certifications or experience. The role often serves as a stepping stone to more senior positions like Clinical Study Manager.

What are the key skills and qualifications needed to thrive as a Clinical Study Manager, and why are they important?

To thrive as a Clinical Study Manager, you need a strong background in clinical research, project management, and regulatory compliance, typically supported by a degree in life sciences and experience in clinical trials. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and certifications like GCP (Good Clinical Practice) are highly valued. Strong organizational, leadership, and communication skills help manage cross-functional teams and ensure study timelines are met. These skills are crucial for maintaining study quality, ensuring regulatory adherence, and delivering successful trial outcomes.

What are some common challenges faced by Clinical Study Managers, and how can they be addressed?

Clinical Study Managers often encounter challenges such as coordinating multiple stakeholders, ensuring regulatory compliance, and managing tight timelines across study sites. Effective communication and proactive planning are essential to address these issues, as well as staying up to date with changing industry regulations. Building strong relationships with site staff and fostering a collaborative team environment can also help mitigate delays and ensure study milestones are met successfully.

Is CRA an entry level job?

A Clinical Research Associate (CRA) is typically not an entry-level position; it usually requires prior experience in clinical research, such as coordinating trials or working in related roles. Entry-level roles in clinical research often include Clinical Trial Assistant or Clinical Research Coordinator, while CRAs often need knowledge of Good Clinical Practice (GCP) and relevant certifications like CCRP or RAC.

What does a clinical study manager do?

A clinical study manager oversees the planning, execution, and monitoring of clinical trials to ensure they comply with regulatory standards and protocols. They coordinate with research teams, manage budgets, and ensure data quality, often using specialized software and requiring strong organizational skills. Their role is essential for the successful completion of clinical research projects.

How much does a clinical trials manager make?

A clinical study manager typically earns between $80,000 and $130,000 annually, depending on experience, location, and the size of the organization. Senior managers or those with specialized skills and certifications can earn higher salaries, often exceeding $150,000. Compensation may also include bonuses and benefits related to project scope and responsibilities.
What are the most commonly searched types of Clinical Study jobs in Virginia? The most popular types of Clinical Study jobs in Virginia are:
What are popular job titles related to Clinical Study Manager jobs in Virginia? For Clinical Study Manager jobs in Virginia, the most frequently searched job titles are:
What job categories do people searching Clinical Study Manager jobs in Virginia look for? The top searched job categories for Clinical Study Manager jobs in Virginia are:
What cities in Virginia are hiring for Clinical Study Manager jobs? Cities in Virginia with the most Clinical Study Manager job openings:
Clinical Study Manager jobs near you
Infographic showing various Clinical Study Manager job openings in Virginia as of July 2026, with employment types broken down into 2% As Needed, 74% Full Time, 17% Part Time, and 7% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $128,919 per year, or $62 per hour.
Clinical Trial & Pharmacovigilance Manager

Clinical Trial & Pharmacovigilance Manager

Venesco LLC

Falls Church, VA • On-site

Full-time

This job post has expired today. Applications are no longer accepted.

Job description

Clinical Trial & Pharmacovigilance Manager
Location: Hybrid
Job Type: Full-Time
About the Role
We are seeking an experienced Clinical Trial & Pharmacovigilance Manager to oversee clinical studies and ensure robust safety surveillance.
Requirements
Key Responsibilities
  • Manage clinical trial operations from startup to closeout
  • Oversee adverse event reporting and pharmacovigilance systems
  • Ensure compliance with GCP and regulatory requirements
  • Coordinate DSMB activities and safety reviews
  • Develop and manage clinical study documentation
  • Collaborate with regulatory teams on submissions

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

Preferred
  • Experience with safety databases (Argus, ArisG)
  • Clinical trial management certification

Apply