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Clinical Operations Associate Jobs in Washington

PharmaOut

Clinical Project Manager

Gaithersburg, MD · On-site

... Associate Director of Clinical Operations along with the US Site Head. Location: Gaithersburg, Maryland Responsibilities: Participates in the planning, implementation and management of pre-IND ...

Mainspring Recovery

Clinical Director

Dumfries, VA · On-site

$125K - $135K/yr

Oversees daily clinical operations across all ASAM levels of care within the facility * Provides clinical supervision and oversight for associate-level and licensed clinical staff in accordance with ...

Backpack Healthcare

Clinical Psychologist

Annapolis, MD · On-site

$87K - $120K/yr

Partner with Clinical, Operations, Billing, Credentialing, and executive leadership to launch and ... Help identify, recruit, onboard, and develop a qualified Psychological Associate. * Provide ...

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Clinical Operations Associate information

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$12

$29

$60

How much do clinical operations associate jobs pay per hour?

As of Sep 11, 2026, the average hourly pay for clinical operations associate in Washington is $29.72, according to ZipRecruiter salary data. Most workers in this role earn between $20.14 and $34.33 per hour, depending on experience, location, and employer.

What is a clinical operations associate?

A Clinical Operations Associate supports the planning, execution, and management of clinical trials to ensure compliance with regulatory guidelines and company protocols. They assist in coordinating trial logistics, managing documentation, and communicating with study sites and stakeholders. Their role helps ensure studies run efficiently, meet regulatory requirements, and generate reliable data for drug development and approvals.

What are the typical responsibilities and team dynamics for a clinical operations associate?

As a Clinical Operations Associate, your typical responsibilities include coordinating study activities, maintaining trial documentation, supporting regulatory submissions, and ensuring adherence to protocols and timelines. You will often work as part of a multi-disciplinary team that includes clinical research coordinators, data managers, and study monitors, frequently communicating with internal and external stakeholders to keep the study on track. Collaboration and adaptability are key, as priorities can shift based on site needs or regulatory updates. This role offers valuable exposure to the operations side of clinical research and can serve as a springboard to more senior roles such as Clinical Project Manager or Clinical Research Associate.

What are the key skills and qualifications needed to thrive in the clinical operations associate position, and why are they important?

To thrive as a Clinical Operations Associate, you need a solid background in clinical research processes, project management, and regulatory compliance, often supported by a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and Good Clinical Practice (GCP) certification is highly valued. Attention to detail, strong organizational skills, and effective communication are important soft skills that help manage complex studies and collaborate with cross-functional teams. These abilities are crucial for ensuring that clinical trials run smoothly, meet regulatory standards, and maintain participant safety.

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

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

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

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

What job categories do people searching Clinical Operations Associate jobs in Washington look for?

The top searched job categories for Clinical Operations Associate jobs in Washington are:

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

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

Clinical Operations Associate jobs near you
Infographic showing various Clinical Operations Associate job openings in Washington as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 9% Part Time, 3% Temporary, 6% Contract, and 1% Nights. Highlights an 89% Physical, 2% Hybrid, and 9% Remote job distribution, with an average salary of $61,827 per year, or $29.7 per hour.

Regulatory Operations Associate

Bethesda, MD • On-site

TRI Challenge Convention
See more jobs at TRI Challenge Conventionexternal

Full-time

Posted 23 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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