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Clinical Trial Management Associate Jobs in Reston, VA

Emmes

Clinical Trial Manager II

Rockville, MD

Overview Clinical Trial Manager II US Remote Emmes Group: Building a better future for us all ... Research Associates (CRAs), CRAs, and site management staff on assigned projects. * Leads ...

REGENXBIO

In-House CRA / Clinical Trial Associate

Rockville, MD · On-site

$34.25 - $46.75/hr

As the In-house CRA you will support and coordinate the logistical aspects of clinical trial management, site management, data review and cleaning according to FDA regulations, Good Clinical Practice ...

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 ...

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 ...

The Emmes Company, LLC

In-House CRA II

Rockville, MD · Remote

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

Emmes

In-House CRA II

Rockville, MD · Remote

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

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Clinical Trial Management Associate information

See Reston, VA salary details

$18

$41

$73

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

As of Jun 12, 2026, the average hourly pay for clinical trial management associate in Reston, VA is $41.68, according to ZipRecruiter salary data. Most workers in this role earn between $33.56 and $45.87 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.

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.

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 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.

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Clinical Trial Management Associate jobs near you
Clinical Trial & Pharmacovigilance Manager

Clinical Trial & Pharmacovigilance Manager

VENESCO, LLC

Falls Church, VA • Hybrid

Other

Posted 5 days ago

Job description

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