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Clinical Trial Operations Manager Jobs in Washington

Ambu

Clinical Trial Manager

Columbia, MD · On-site

Clinical Trial Manager City: Columbia, MD Country/Region: United States State: Business Area ... Serve as the primary operational liaison between clinical sites, investigators, internal ...

IQVIA

Clinical Trial Rater

Washington, DC · Remote

Clinical Trial Rater - Borderline Personality Disorder (BPD) Location: Remote based in the US Hours: Approximately 5h per week Role: Clinical Specialist Start: immediate Contract based About IQVIA ...

Guidehouse

Clinical Program Manager

Bethesda, MD · On-site

$85K - $141K/yr

Clinical Trial Operations Travel Required: None Clearance Required: Ability to Obtain Public Trust What You Will Do: We are currently searching for a Clinical Program Manger to support complex ...

Guidehouse

Clinical Program Manager

Bethesda, MD · On-site

$85K - $141K/yr

Clinical Trial Operations Travel Required: None Clearance Required: Ability to Obtain Public Trust What You Will Do: We are currently searching for a Clinical Program Manger to support complex ...

Vivo HealthStaff

Clinical Trial Physician

Washington, DC · On-site

$110 - $140/hr

Vivo HealthStaff is recruiting for a Clinical Trials Physician for a Vaccine Trial in the USA ... We are seeking an experienced and licensed Pain Management Physician to provide locum tenens ...

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Clinical Trial Operations Manager information

See Washington salary details

$32

$70

$108

How much do clinical trial operations manager jobs pay per hour?

As of Sep 3, 2026, the average hourly pay for clinical trial operations 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 does a clinical trial operations manager do?

A Clinical Trial Operations Manager oversees the planning, execution, and completion of clinical trials to ensure they are conducted efficiently, ethically, and in compliance with regulatory standards. They coordinate with cross-functional teams, manage budgets and timelines, and handle any issues that arise during the trial process. This role is crucial for ensuring that new drugs or medical devices are tested safely and effectively before reaching the market.

What are the key skills and qualifications needed to thrive as a clinical trial operations manager, and why are they important?

To thrive as a Clinical Trial Operations Manager, you need a strong background in clinical research, regulatory compliance, project management, and a relevant degree such as in life sciences or healthcare. Familiarity with clinical trial management systems (CTMS), Good Clinical Practice (GCP) guidelines, and certifications like ACRP or SOCRA are highly valued. Leadership, attention to detail, and effective communication are essential soft skills for coordinating teams and stakeholders. These competencies ensure clinical trials are conducted efficiently, ethically, and in accordance with regulatory requirements.

What are some common challenges faced by clinical trial operations managers, and how can they be addressed?

Clinical Trial Operations Managers often encounter challenges such as ensuring regulatory compliance across multiple sites, managing tight timelines, and coordinating diverse teams. Effective communication and proactive planning are essential to address these difficulties. Leveraging project management tools and fostering strong relationships with investigators and site staff can also help streamline operations and reduce risks of delays or protocol deviations.

What is the difference between Clinical Trial Operations Manager vs Clinical Research Coordinator?

AspectClinical Trial Operations ManagerClinical Research Coordinator
CredentialsBachelor's degree; often advanced degrees or certifications in clinical research or managementBachelor's degree in health sciences or related field; certifications like CCRP are common
Work EnvironmentOversees multiple trials, manages teams, and coordinates with stakeholders in clinical settingsWorks directly with participants, manages trial documentation, and supports daily trial activities
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsHospitals, clinics, research institutions

The Clinical Trial Operations Manager focuses on overseeing entire clinical trial processes, managing teams, and ensuring compliance across multiple studies. In contrast, the Clinical Research Coordinator handles the day-to-day activities at the trial site, working closely with participants and supporting trial documentation. Both roles require relevant certifications and are essential in the clinical research industry, but they differ in scope and responsibilities.

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

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

What cities in Washington are hiring for Clinical Trial Operations Manager jobs?

Cities in Washington with the most Clinical Trial Operations Manager job openings:

Clinical Trial Operations Manager jobs near you
Infographic showing various Clinical Trial Operations Manager job openings in Washington as of August 2026, with employment types broken down into 87% Full Time, 11% Part Time, and 2% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% 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 • On-site

Full-time

Re-posted 22 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