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Clinical Trials Associate Jobs in Washington (NOW HIRING)

The Safety Associate focuses on managing and analyzing safety-related data under supervision ... General knowledge of the drug and vaccine development process or clinical trials is a plus. B.A./B.

... trials and accelerating the development of life-changing therapies.We believe that every clinical ... The Clinical Research Associate (CRA) II is responsible for monitoring clinical study sites either ...

Study Start-Up Associate II

Rockville, MD · On-site +1

$34.25 - $46.75/hr

Overview Study Start-Up Associate II US Remote Emmes Group: Building a better future for us all ... clinical trials. Gets involved in creation, filing, and updating of trackers and templatesand ...

As an Associate Director, Biostatistician, you will be a champion of Otsuka's culture and values ... Experience with early phase clinical trials, preferably firstinhuman or PK/PD/biomarkerfocused ...

Senior Clinical Research Associate - Oncology (Myelofibrosis) - West Region ICON is a global health ... Experienced monitoring Oncology specifically Myelofibrosis clinical trials. * Proficient in ICH-GCP ...

The Senior In-House Clinical Research Associate (CRA) is responsible for assisting with operational activities supporting the site management and monitoring of clinical studies/trials, ensuring ...

The Senior In-House Clinical Research Associate (CRA) is responsible for assisting with operational activities supporting the site management and monitoring of clinical studies/trials, ensuring ...

Showing results 21-40

Clinical Trials Associate information

See Washington salary details

$19

$45

$79

How much do clinical trials associate jobs pay per hour?

As of Sep 2, 2026, the average hourly pay for clinical trials 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 is a clinical trials associate?

Clinical Trials Associates (CTAs) are professionals who support the planning, coordination, and administration of clinical research studies, often working under the supervision of Clinical Research Coordinators or Managers. Their responsibilities typically include maintaining study documentation, ensuring regulatory compliance, assisting with data collection, and communicating with study sites. CTAs play a critical role in ensuring that clinical trials run smoothly and adhere to strict protocols and guidelines. Their work helps bring new medical treatments and therapies to market safely and efficiently.

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

To thrive as a Clinical Trials Associate, you need a solid understanding of clinical research protocols, regulatory compliance, and data management, typically supported by a life sciences degree. Familiarity with systems such as electronic data capture (EDC), clinical trial management systems (CTMS), and knowledge of Good Clinical Practice (GCP) guidelines or related certifications is important. Strong organizational skills, attention to detail, and effective communication help you excel in coordinating study activities and collaborating with diverse teams. These skills ensure accurate trial execution, regulatory adherence, and successful study outcomes.

What are some common challenges faced by clinical trials associates, and how can they be managed effectively?

Clinical Trials Associates often face challenges such as coordinating with multiple stakeholders, managing tight deadlines, and ensuring strict compliance with regulatory guidelines. Balancing administrative tasks with participant communication requires strong organizational skills and attention to detail. Staying proactive in communication, utilizing project management tools, and seeking guidance from senior team members can help manage these challenges effectively while fostering a collaborative team environment.

What is the difference between Clinical Trials Associate vs Clinical Research Coordinator?

AspectClinical Trials AssociateClinical Research Coordinator
CredentialsBachelor's degree, often in life sciences; certifications like ACRP or SOCRA are commonBachelor's degree in health sciences or related field; certifications like CCRP are advantageous
Work EnvironmentTypically works in clinical trial sites, pharmaceutical companies, or CROsWorks directly at clinical sites, hospitals, or research centers
Job FocusSupports trial setup, data entry, and regulatory complianceManages patient recruitment, scheduling, and data collection

While both roles support clinical research, Clinical Trials Associates primarily focus on trial logistics and compliance, whereas Clinical Research Coordinators handle patient interactions and site management. Both positions require similar educational backgrounds and certifications, often working in the same environments, but their daily responsibilities differ.

Is a clinical trials associate a good career?

A clinical trials associate is a valuable role in the healthcare and pharmaceutical industries, responsible for coordinating and monitoring clinical trial activities. It offers opportunities for career growth, requires attention to detail, and often involves working with regulatory guidelines and data management tools. The role can be stable and rewarding for those interested in medical research and patient safety.

What do I need to be a clinical trials associate?

To become a clinical trials associate, candidates typically need a bachelor's degree in life sciences, healthcare, or a related field. Relevant skills include knowledge of Good Clinical Practice (GCP), attention to detail, and experience with clinical trial management systems or regulatory documentation. Certifications such as the Certified Clinical Research Professional (CCRP) can enhance job prospects.

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

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

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

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

Infographic showing various Clinical Trials Associate job openings in Washington as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $94,197 per year, or $45.3 per hour.

Associate Director, Digital Health MedTech Clinical

IQVIA

Washington, DC • On-site, Remote

Full-time

Posted 11 days ago


IQVIA rating

8.1

Company rating: 8.1 out of 10

Based on 53 frontline employees who took The Breakroom Quiz

62nd of 226 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 Overview

The Associate Director, Digital Health Studies provides senior leadership for the delivery of digital health clinical research programs, including decentralized and hybrid clinical trials, connected devices, digital therapeutics, AI-enabled healthcare technologies, wearable solutions, and other technology-enabled study models.

This role serves as a sponsor-facing leader responsible for clinical oversight, operational excellence, and cross-functional collaboration across the study lifecycle. The Associate Director will play a key role in growing and scaling IQVIA's Digital Health practice by ensuring high-quality execution, supporting business development efforts, and developing organizational capabilities in this rapidly evolving area.

Key ResponsibilitiesClinical & Operational Leadership
  • Provide leadership and oversight for digital health clinical studies from study start-up through closeout.
  • Ensure studies are executed in compliance with ICH-GCP, regulatory requirements, and company quality standards.
  • Serve as the escalation point for clinical, operational, quality, and technology-related issues.
  • Drive consistency and best practices across digital health study delivery.
Sponsor & Stakeholder Management
  • Serve as a primary point of contact for sponsors and senior stakeholders.
  • Lead governance meetings, study reviews, and executive-level communications.
  • Build and maintain strong relationships with sponsors, investigators, vendors, and cross-functional teams.
Practice Growth & Business Development
  • Support proposals, bid defenses, and client presentations.
  • Provide subject-matter expertise across digital health, decentralized clinical trials, connected devices, and emerging healthcare technologies.
  • Contribute to the development of scalable delivery models and service offerings.
People Leadership
  • Mentor and develop project managers, clinical staff, and study teams.
  • Support hiring, onboarding, and professional development initiatives.
  • Foster a culture of accountability, collaboration, and continuous improvement.
QualificationsRequired
  • Bachelor's degree in Life Sciences, Healthcare, Public Health, Nursing, Technology, or a related field.Advanced scientific, clinical, public health, or related healthcare discipline strongly preferred.
  • 7+ years of clinical research experience, including experience supporting digital health, medical device, or technology-enabled clinical studies.
  • Experience leading complex, multi-study clinical research programs.
  • Strong understanding of ICH-GCP, clinical trial operations, and regulatory requirements.
Preferred
  • Experience with decentralized and hybrid clinical trial models.
  • Experience supporting one or more of the following:
    • Digital Therapeutics (DTx)
    • Connected Medical Devices
    • Software as a Medical Device (SaMD)
    • AI-Enabled Healthcare Solutions
    • Wearable Technologies
    • Remote Patient Monitoring
    • Radiology or Imaging Technologies
  • Familiarity with EDC, CTMS, ePRO, and other clinical technology platforms.
Competencies
  • Strong leadership and client management skills.
  • Excellent communication and presentation abilities.
  • Ability to manage multiple priorities in a fast-paced environment.
  • Strong problem-solving and decision-making capabilities.
  • Advanced proficiency with Microsoft Office applications

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 $102,500.00 - $285,500.00. 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.

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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