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Clinical Monitoring Associate Jobs in Washington

IQVIA

MedTech Site Manager 1

Washington, DC · On-site

$74K - $124K/yr

Position Overview The In-House Clinical Research Associate/MedTech Site Manager 1 will be a ... Ensure that monitoring activities (remote and on-site) are completed in accordance with company ...

New

IQVIA

MedTech Site Manager 1

Washington, DC

$74K - $124K/yr

Position Overview The In-House Clinical Research Associate/MedTech Site Manager 1 will be a ... Ensure that monitoring activities (remote and on-site) are completed in accordance with company ...

New

MBI Health Services

ACT Associate Director

Washington, DC · On-site

$90K - $105K/yr

Collaborate with the Director to provide clinical monitoring and support to multidisciplinary staff ... The Associate Director will maintain a team of no more than 9 Recovery Support Specialists and will ...

ICON

Senior Clinical Research Associate

Washington, DC · On-site +1

$110K - $138K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Senior Clinical Research Associate - Oncology - Washington DC ICON is a global healthcare ... Perform remote and on-site monitoring/co-monitoring visits (Site Qualification Visits, Site ...

Icon plc

Senior Clinical Research Associate

Washington, DC · Hybrid

$110K - $138K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Senior Clinical Research Associate - Oncology - Washington DC ICON is a global healthcare ... Promptly document monitoring activitiesandsubmit/approvevisit reports * Manage site essential ...

Emmes

Senior Clinical Research Associate

Rockville, MD · On-site +1

  • Medical

  • Retirement

Overview Senior Clinical Research Associate US remotely and on-site (80% travel) Emmes Group ... The CRA will conduct monitoring visits and activities in accordance with Emmes SOPs, applicable ...

Emmes

Sr. Clinical Research Associate

Rockville, MD · On-site +1

The CRA will conduct monitoring visits and activities in accordance with Emmes SOPs, applicable regulations, and ICH GCP. Responsibilities * Under minimal supervision of the project CRA staff ...

Abbott

Clinical Associate

Arlington, VA · On-site

  • Medical

  • Retirement

Exercises independent judgment in planning, organizing and performing work; monitors performance and reports status to manager. As a Clinical Associate on the U.S. Abbott EP team, you will provide ...

Abbott

Clinical Associate

Arlington, VA · On-site

  • Medical

  • Retirement

Exercises independent judgment in planning, organizing and performing work; monitors performance and reports status to manager. As a Clinical Associate on the U.S. Abbott EP team, you will provide ...

Icon plc

Sr. Clinical Research Associate

Washington, DC

$110K - $138K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Senior Clinical Research Associate - Oncology (Myelofibrosis) - West Region ICON is a global health ... Monitor patient safety, ensuring timely and accurate AE/SAE/PQC reporting * Support subject ...

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Clinical Monitoring Associate information

See Washington salary details

$14

$35

$62

How much do clinical monitoring associate jobs pay per hour?

As of Aug 16, 2026, the average hourly pay for clinical monitoring associate in Washington is $35.72, according to ZipRecruiter salary data. Most workers in this role earn between $23.94 and $47.12 per hour, depending on experience, location, and employer.

How does a clinical monitoring associate typically collaborate with clinical research teams during a study?

Clinical Monitoring Associates (CMAs) work closely with clinical research teams, including Clinical Research Associates (CRAs), project managers, and site staff. They support the coordination of study activities by tracking site progress, preparing essential documentation, and helping resolve site queries. CMAs often participate in regular team meetings, communicate updates, and ensure accurate data collection and compliance with study protocols. This collaborative environment helps ensure that clinical trials run smoothly and meet regulatory requirements.

What is a clinical monitoring associate?

Clinical Monitoring Associates (CMAs) are professionals who support the conduct of clinical trials by assisting with the monitoring of study sites to ensure compliance with protocols, regulatory requirements, and good clinical practice guidelines. They work closely with Clinical Research Associates and study coordinators to track the progress of trials, verify data accuracy, and manage documentation. CMAs play a crucial role in maintaining data integrity and patient safety throughout the clinical research process.

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

To thrive as a Clinical Monitoring Associate, you need a background in life sciences, familiarity with Good Clinical Practice (GCP) guidelines, and a relevant bachelor's degree. Experience with clinical trial management systems (CTMS), electronic data capture (EDC), and certifications in clinical research (such as ACRP or SOCRA) are often required. Strong attention to detail, organizational skills, and effective communication help you excel in site management and ensure protocol adherence. These competencies are crucial for maintaining regulatory compliance, ensuring patient safety, and supporting the successful execution of clinical trials.

What cities in Washington are hiring for Clinical Monitoring Associate jobs?

Cities in Washington with the most Clinical Monitoring Associate job openings:

Clinical Monitoring Associate jobs near you

MedTech Site Manager 1

IQVIA

Washington, DC • On-site

$74K - $124K/yr

Full-time

Posted yesterday

New

IQVIA rating

8.1

Company rating: 8.1 out of 10

Based on 53 frontline employees who took The Breakroom Quiz

62nd of 224 rated it services

Job description

MCRA is part of IQVIA MedTech. As a trusted CRO and advisory partner, IQVIA MedTech and MCRA deliver integrated lifecycle solutions for the medical device and diagnostics industry. Together, we support innovation from concept to commercialization, offering expertise in regulatory strategy, clinical trial design and execution, market access, and post-market optimization. Our teams combine deep therapeutic knowledge with advanced data and technology to help clients make smarter decisions and thrive in the market. Join our team to help shape the future of MedTech.Position OverviewThe In-House Clinical Research Associate/MedTech Site Manager 1 will be a critical team member reporting directly to the Director of Clinical Affairs, to support 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 execute Clinical Affairs functions in accordance with Good Clinical Practice (GCP) guidelines, Standard Operating Procedures (SOPs), and any other applicable regulatory requirements.Position Responsibilities
  • Review and approve research and study regulatory documents required for the implementation, monitoring, and evaluation of clinical trials.
  • Review clinical protocols to ensure collection of data needed for regulatory submissions
  • Contribute to protocol-specific manuals, plans, and documents as needed.
  • Ensure that monitoring activities (remote and on-site) are completed in accordance with company/client SOPs and Clinical Monitoring Plan.
  • Assist project manager with clinical study planning and management, as required.
  • Develop and maintain positive relationships both internal and external to project, including clients, team members, and site personnel (PIs, Study coordinators, etc.).
  • Assist in the identification and recruitment of potential investigators and study sites, as needed.
  • Ensure Trial Master File is accurate and complete throughout the lifecycle of the project.
  • Assist with site training for assigned clinical trials.
  • Assist with site audits and site quality management activities as needed.
  • Maintain current knowledge of GCP and FDA guidance as it relates to clinical research, as well as current clinical related developments in the assigned therapeutic areas.
Required Qualifications
  • Bachelor's degree (B.A./B.S.) in pharmacy, pharmaceutics or a related scientific discipline
  • 2+ years of clinical trial experience. Monitoring experience preferred.
  • Comprehensive knowledge/ fluency of GCPs and clinical monitoring procedures
  • Understanding of therapeutic area for assigned clinical projects.
  • Experience using Electronic Data Capture (EDC) and clinical trial management systems.
  • Possesses strong written and verbal communication and presentation skills.
  • Strong research, analytical, critical-thinking and problem solving skills
  • PC/Technical skills - MS Office, Excel, Word, PowerPoint (Endnote experience is a plus)

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more athttps://jobs.iqvia.com

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

The potential base pay range for this role, when annualized, is $74,500.00 - $124,100.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

What IQVIA employees say

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About IQVIA

Sourced by ZipRecruiter

At IQVIA, we are passionate about helping customers and partners improve results and patient outcomes. Everything we do contributes to this vision for creating a healthier world. In today’s healthcare environment, it’s not only about how much data, information, and technology you have at your fingertips – it’s what you do with it. IQVIA is focused on making intelligent connections for customers across the entire healthcare ecosystem to help you drive healthcare forward. Whether that means partnering with novel technology companies to boost patient engagement, leveraging AI & machine learning to accelerate results, or using decentralized trials to reach the right patients wherever they are – we are always looking for smarter ways to move you forward.

Industry

Health care and social assistance

Company size

10,000+ Employees

Headquarters location

Durham, NC, US

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