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Clinical Trial Management Associate Jobs in Washington

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 ...

Axle

Clinical Research Coordinator

Bethesda, MD · On-site

$26 - $34.50/hr

Experience with clinical trial management systems and research databases, technology transfer or clinical trial agreements, and supporting NIH, NCI, academic medical centers, or federally funded ...

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 ...

Guidehouse

Clinical Program Manager

Bethesda, MD · On-site

$85K - $141K/yr

Experience with clinical trial management systems and research databases. * Experience with technology transfer agreements, clinical trial agreements, cooperative research and development agreements ...

Emmes Group

Sr. In-House CRA

Rockville, MD · On-site

The Sr. In-House CRA may also be referred to as a Clinical Trial Associate on some contracts. Responsibilities * Under the high level supervision of the project site management staff oversight lead ...

IQVIA

Clinical Trial Psych Rater

Fairfax, VA · Remote

$62K - $156K/yr

Clinical Trial Psych Rater - US Spanish Speaking Location: Remote/Virtual Hours: Estimated 10-16 ... Excellent organizational skills, attention to detail, time management, and problem-solving ability.

Emmes

Sr. In-House CRA

Rockville, MD · On-site +1

The Sr. In-House CRA may also be referred to as a Clinical Trial Associate on some contracts. Responsibilities * Under the high level supervision of the project site management staff oversight lead ...

The Emmes Company, LLC

Sr. In-House CRA

Rockville, MD · On-site

The Sr. In-House CRA may also be referred to as a Clinical Trial Associate on some contracts. Responsibilities * Under the high level supervision of the project site management staff oversight lead ...

Emmes

Sr. In-House CRA

Rockville, MD · On-site

$100 - $125/hr

The Sr. In-House CRA may also be referred to as a Clinical Trial Associate on some contracts. Responsibilities * Under the high level supervision of the project site management staff oversight lead ...

IQVIA

MedTech Site Manager 1

Washington, DC

$74K - $124K/yr

... clinical trial operations for the firm's clientele. Responsible for management of investigator site and Clinical Research Associate (CRA) activities for assigned studies. The In-House CRA will ...

IQVIA

MedTech Site Manager 1

Washington, DC

$74K - $124K/yr

... clinical trial operations for the firm's clientele. Responsible for management of investigator site and Clinical Research Associate (CRA) activities for assigned studies. The In-House CRA will ...

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Clinical Trial Management Associate information

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How much do clinical trial management associate jobs pay per hour?

As of Sep 7, 2026, the average hourly pay for clinical trial management associate in Washington is $45.29, according to ZipRecruiter salary data. Most workers in this role earn between $36.49 and $49.81 per hour, depending on experience, location, and employer.

What does a clinical trial management associate do?

A Clinical Trial Management Associate (CTMA) is responsible for supporting the planning, execution, and monitoring of clinical trials to ensure they run smoothly and comply with regulatory requirements. CTMAs coordinate between study sites, vendors, and internal teams to manage documentation, timelines, and trial logistics. They also help ensure data integrity and assist in resolving any issues that may arise during the trial process. This role is essential for the successful completion of clinical research studies in the pharmaceutical and biotechnology industries.

How does a clinical trial management associate typically collaborate with cross-functional teams during a clinical study?

As a Clinical Trial Management Associate, you’ll work closely with various cross-functional teams, including clinical operations, data management, regulatory affairs, and site staff. Your role often involves scheduling and coordinating meetings, tracking study progress, and ensuring all documentation and project timelines are up to date. Effective communication is critical, as you'll need to relay updates, resolve issues, and keep stakeholders aligned throughout the clinical trial process. This collaborative environment fosters learning and provides insight into multiple aspects of clinical research, helping you develop a well-rounded skill set.

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

To thrive as a Clinical Trial Management Associate, you need a strong background in life sciences or a related field, along with knowledge of clinical research regulations and trial processes. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and Good Clinical Practice (GCP) certification are typically required. Excellent organizational skills, attention to detail, and effective communication are essential soft skills for managing study timelines and collaborating with cross-functional teams. These competencies ensure that clinical trials are conducted efficiently, compliantly, and successfully, supporting critical advancements in healthcare.

What is the difference between Clinical Trial Management Associate vs Clinical Research Coordinator?

AspectClinical Trial Management AssociateClinical Research Coordinator
CredentialsBachelor's degree often required; certifications like CCRP beneficialBachelor's degree; certifications like CCRP or CCRC advantageous
Work EnvironmentPharmaceutical companies, CROs, or biotech firmsHospitals, clinics, or research sites
ResponsibilitiesOverseeing trial logistics, compliance, and documentationPatient recruitment, data collection, and site management
Industry UsageCommon in clinical trial management teamsCommon in research sites and hospitals

The Clinical Trial Management Associate primarily focuses on managing trial logistics and compliance within pharmaceutical or biotech settings, while the Clinical Research Coordinator handles patient interactions and data collection at research sites. Both roles require similar educational backgrounds and certifications, but their work environments and specific responsibilities differ.

What are popular job titles related to Clinical Trial Management Associate jobs in Washington?

For Clinical Trial Management Associate jobs in Washington, the most frequently searched job titles are:

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What cities in Washington are hiring for Clinical Trial Management Associate jobs?

Cities in Washington with the most Clinical Trial Management Associate job openings:

Clinical Trial Management Associate jobs near you
Infographic showing various Clinical Trial Management Associate job openings in Washington as of August 2026, with employment types broken down into 1% As Needed, 83% Full Time, 13% Part Time, and 3% Contract. Highlights an 83% Physical, 2% Hybrid, and 15% Remote job distribution, with an average salary of $94,197 per year, or $45.3 per hour.

Clinical Trial & Pharmacovigilance Manager

VENESCO, LLC

Falls Church, VA • Hybrid

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

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