1

Clinical Study Manager Jobs in Washington (NOW HIRING)

... study sites either onsite at investigative sites or remotely to ensure clinical trials are ... CRA, Project Manager, etc., independently schedules and conducts remote and on-site monitoring ...

Showing results 21-40

Clinical Study Manager information

See Washington salary details

$32

$70

$108

How much do clinical study manager jobs pay per hour?

As of Sep 1, 2026, the average hourly pay for clinical study manager in Washington is $70.81, according to ZipRecruiter salary data. Most workers in this role earn between $57.45 and $79.76 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a clinical study manager?

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.

How much does a clinical study manager earn?

A clinical study manager's salary varies based on experience, location, and the size of the organization, but typically ranges from $80,000 to $130,000 annually. Senior roles or those with specialized skills and certifications can earn higher salaries, often exceeding $150,000. The position often requires knowledge of regulatory guidelines and project management tools.

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 timelines and budgets, and ensure data quality, often using specialized software and requiring knowledge of Good Clinical Practice (GCP) guidelines.

What are the most commonly searched types of Clinical Study jobs in Washington?

The most popular types of Clinical Study jobs in Washington are:

What are popular job titles related to Clinical Study Manager jobs in Washington?

For Clinical Study Manager jobs in Washington, the most frequently searched job titles are:

What cities in Washington are hiring for Clinical Study Manager jobs?

Cities in Washington with the most Clinical Study Manager job openings:

Infographic showing various Clinical Study Manager job openings in Washington as of August 2026, with employment types broken down into 84% Full Time, 9% Part Time, 2% Temporary, and 5% Contract. Highlights an 77% Physical, 2% Hybrid, and 21% Remote job distribution, with an average salary of $147,276 per year, or $70.8 per hour.

Clinical Trial & Pharmacovigilance Manager

VENESCO LLC

Falls Church, VA โ€ข On-site

Full-time

Re-posted 21 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