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Clinical Study Associate Jobs in Washington (NOW HIRING)

The Emmes Company, LLC

Sr. In-House CRA

Rockville, MD · On-site

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 ...

Emmes

Sr. In-House CRA

Rockville, MD · On-site +1

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 ...

Icon plc

Senior Clinical Research Associate

Washington, DC · On-site

$110K - $138K/yr

Senior Clinical Research Associate - Cardiovascular Device - Central/West Region ICON is a global ... A well-executed plan for communication with the study teams and sites. * Well-versed in clinical ...

Otsuka

Associate Director, Biostatistics

Rockville, MD · On-site +1

As an Associate Director, Biostatistician, you will be a champion of Otsuka's culture and values ... Demonstrated experience leading Phase 1 and early-phase clinical studies, including FIH, dose ...

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Clinical Study Associate information

See Washington salary details

$14

$35

$62

How much do clinical study associate jobs pay per hour?

As of Sep 2, 2026, the average hourly pay for clinical study 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.

What is a clinical study associate?

Clinical Study Associates (CSAs) are professionals who support the planning, execution, and monitoring of clinical trials in the pharmaceutical, biotechnology, or medical device industries. They help coordinate study logistics, maintain study documentation, and ensure compliance with regulatory requirements. CSAs often work closely with Clinical Research Associates, study coordinators, and investigators to ensure that trials are conducted according to protocol and timelines. Their role is essential in ensuring the accuracy and integrity of data collected during clinical research.

What are some common challenges clinical study associates face when managing multiple clinical trials simultaneously?

Clinical Study Associates often juggle several clinical trials at once, which can present challenges such as prioritizing competing deadlines, maintaining accurate documentation for each study, and ensuring consistent communication with cross-functional teams. Staying organized and proactive is essential, as unforeseen protocol amendments or site issues can arise. Building strong relationships with site staff and utilizing effective project management tools can help CSAs navigate these complexities and deliver high-quality results.

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

To thrive as a Clinical Study Associate, you need a strong understanding of clinical research processes, regulatory requirements, and typically a life sciences degree. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and GCP certification are commonly required. Attention to detail, organizational skills, and effective communication set top performers apart in this role. These competencies ensure accurate study documentation, regulatory compliance, and smooth coordination across research teams.

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

AspectClinical Study AssociateClinical Research Coordinator
CredentialsBachelor's degree, often in life sciences; certifications like CCRP or CCRA beneficialBachelor's degree in health sciences or related field; certifications like CCRP advantageous
Work EnvironmentPharmaceutical companies, CROs, clinical trial sitesHospitals, clinics, research centers
Job FocusMonitoring clinical trials, ensuring protocol compliance, data accuracyManaging daily trial activities, patient recruitment, data collection
Employer & Industry UsageCommonly employed in pharma and CROsPrimarily in healthcare and academic research settings

Both roles involve clinical trial oversight but differ in focus: Clinical Study Associates primarily monitor and ensure compliance during trials, while Clinical Research Coordinators manage daily trial operations and patient interactions. Understanding these distinctions helps in choosing the right career path or job search focus.

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

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

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

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

Clinical Study Associate jobs near you
Infographic showing various Clinical Study Associate job openings in Washington as of August 2026, with employment types broken down into 3% As Needed, 74% Full Time, 15% Part Time, and 8% Contract. Highlights an 85% Physical, 1% Hybrid, and 14% Remote job distribution, with an average salary of $74,302 per year, or $35.7 per hour.

Senior Specialist Programmer

Fladger Associates

Gaithersburg, MD • On-site

Contractor

Re-posted 23 days ago

Job description

Gaithersburg, MD
Contract Duration: 12-36 months
Rate: Negotiable

Responsibilities:

  • Excellent employment opportunity for a Senior Specialist Programmer in the Gaithersburg, MD area. (100% remote)
  • The Senior Statistical Programmer is a delivery focused role responsible for programming deliverables with quality and timeliness, following established standards and processes.
  • This position requires high technical skills and thorough industry knowledge to independently perform the programming tasks while using judgement about seeking guidance in complex situations.
  • They can be responsible for leading the programming deliveries of clinical studies or small to medium sized clinical projects and can lead cross-functional teams to deliver continuous improvement
  • Primarily responsible for coordinating the various tools for collecting different types of data.
  • Responsible for ensuring databases are created and adjusted for the end user.
  • Contributes to the development and maintenance of analysis and reporting applications.
  • Able to solve complex problems within own area and will participate in a range of projects.
  • Responsible for leading the programming deliveries of a clinical study or a small to medium sized and complex clinical project
  • Implements statistical programming aspects of the protocol or clinical development program
  • Ensures high quality is built into own deliverables and the quality delivered by other programmers
  • Programs independently with high efficiency and quality
  • Writes specifications and oversee completeness of relevant documentation
  • Contributes to or drives the development of best practices to improve quality, efficiency and effectiveness within function
  • Ensures compliance to standards and automation usage
  • Plans and leads team activities and tasks
  • Identifies, manages and communicates risk within the assigned studies and/or projects
  • Works proactively with study team members including but not limited to the statistician, lead programmer, data manager and study leader
  • Works cooperatively with contract programming providers
  • Influences stakeholders by providing subject matter expertise on programming related items
  • Contributes to or leads technical initiatives
  • Employs Project Management practices in managing programming aspects of drug or technical projects
Experience:
  • Vaccine experience highly desired
  • Bachelor's Degree in Mathematics (i.e., Applied Math, Engineering, etc.), Statistics, Computer Science, Life Science or equivalent
  • 8-10 years of strong Programming experience
    Ability to proactively manage concurrent activities within a study or part of project
  • Excellent programming skills including macro language
  • Proficient knowledge of the clinical development process
  • Thorough knowledge of industry standards
  • Ability to apply Programming knowledge to problem solving
  • Ability to manage relevant documentation
  • Ability to influence relevant stakeholders on Programming related items
  • Ideally candidate would have previous vaccine experience.
  • Ability to proactively manage concurrent activities within a study or part of project