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Clinical Trials Associate Jobs in Washington (NOW HIRING)

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 ... clinical trials. * Review clinical protocols to ensure collection of data needed for regulatory ...

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 ... clinical trials. * Review clinical protocols to ensure collection of data needed for regulatory ...

Prism Vision Group

Clinical Research Assistant

Fairfax, VA · On-site

$46K - $96K/yr

Obtains informed consent from patients and conducts study visits for clinical trials * Creates Case ... Associates or Bachelors Degree preferred in Science or related field. Equivalent relevant ...

System One

Manufacturing Associate

Rockville, MD · On-site

$18 - $25/hr

Participate in hands-on manufacturing of materials for clinical trials in a GMP environment ... or Associate's degree in a related discipline with no experience. Experience with aseptic ...

System One

Manufacturing Associate

Rockville, MD · On-site

$18 - $25/hr

Participate in hands-on manufacturing of materials for clinical trials in a GMP environment ... or Associate's degree in a related discipline with no experience. Experience with aseptic ...

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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:

Clinical Trials Associate jobs near you
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.

Regulatory Operations Associate

TRI Challenge Convention

Bethesda, MD

Full-time

Posted 14 days ago

Job description

Prepare standard documentation supporting regulatory filings and distribution to stakeholders. Utilize and maintain hard copy and electronic filing systems for auditable regulatory documents. Maintain effective high-profile communications and interactions with colleagues, collaborators, and clients as appropriate.

Draft, edit, and distribute various documents as needed based on templates and work instructions. Develop and maintain work process tools to promote efficiency and productivity. These may include templates, SOPs, work instructions, checklists, etc.

Track regulatory activity, maintain, and update databases, and ensure that records are complete and current. Provide other administrative regulatory support as needed.Excellent oral and written communication skills; detail-oriented and able to multi-task/prioritize well. Superior organizational skills and customer service abilities are required

Experience publishing regulatory submissions using electronic submission software and proficiency in preparing documents that are compliant with electronic submission standards is preferred. Proficiency in MS Office (Word, Excel, and Outlook); experience with SharePoint is a plus. Must be able to exercise initiative and sound judgment, and to prioritize ongoing projects.

Familiarity with Good Clinical Practices and/or experience of working in an FDA-regulated environment is desirable. General knowledge of the drug and vaccine development process or clinical trials is a plus.Excellent oral and written communication skills; detail-oriented and able to multi-task/prioritize well. Superior organizational skills and customer service abilities are required

Experience publishing regulatory submissions using electronic submission software and proficiency in preparing documents that are compliant with electronic submission standards is preferred. Proficiency in MS Office (Word, Excel, and Outlook); experience with SharePoint is a plus. Must be able to exercise initiative and sound judgment, and to prioritize ongoing projects.

Familiarity with Good Clinical Practices and/or experience of working in an FDA-regulated environment is desirable. General knowledge of the drug and vaccine development process or clinical trials is a plus.

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