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Clinical Study Associate Jobs in Reston, VA (NOW HIRING)

Emmes

Senior Biostatistician

Rockville, MD · On-site +1

May supervise Biostatisticians, Associate Biostatisticians and SAS programmers (all levels) and direct their work on clinical research studies. * Leads the project team's development of study ...

Emmes Group

Senior Biostatistician

Rockville, MD · On-site

May supervise Biostatisticians, Associate Biostatisticians and SAS programmers (all levels) and direct their work on clinical research studies. * Leads the project team's development of study ...

IQVIA

MedTech Site Manager 1

Washington, DC

$74K - $124K/yr

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 ...

IQVIA

MedTech Site Manager 1

Washington, DC · On-site

$74K - $124K/yr

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 ...

Otsuka

Director, Global Clinical Development

Rockville, MD · On-site +1

$209K - $313K/yr

Acts as the signatory on NDA submissions and clinical study and safety documents. * Involved in ... Associate Director level; 3-6 years for Director is typically required depending on type of ...

LeoForce

Oncology CRA-Sponsor side!

Rockville, MD · On-site

$125 - $140/hr

... 1 Clinical Research Associate's (CRA) to join our biotech startup. This is a full-time position ... are compliant with the study protocol, FDA regulations, and other applicable regulatory ...

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Clinical Study Associate information

See Reston, VA salary details

$13

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$57

How much do clinical study associate jobs pay per hour?

As of Sep 8, 2026, the average hourly pay for clinical study associate in Reston, VA is $32.81, according to ZipRecruiter salary data. Most workers in this role earn between $22.02 and $43.27 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 Reston, VA?

The most popular types of Clinical Study jobs in Reston, VA are:

What cities near Reston, VA are hiring for Clinical Study Associate jobs?

Cities near Reston, VA with the most Clinical Study Associate job openings:

Clinical Study Associate jobs near you
Infographic showing various Clinical Study Associate job openings in Reston, VA as of August 2026, with employment types broken down into 2% As Needed, 75% Full Time, 17% Part Time, and 6% Contract. Highlights an 84% Physical, 1% Hybrid, and 15% Remote job distribution, with an average salary of $68,251 per year, or $32.8 per hour.

Senior Biostatistician

Rockville, MD • On-site, Remote

Emmes
Scientific Research and Development Services • 201 - 500 employees
Learn more about Emmesexternal

Full-time

Medical, Retirement

Re-posted 10 days ago

Job description

Overview

Senior Biostatistician

US Remote

Emmes Group: Building a better future for us all.

Emmes Group is transforming the future of clinical research, bringing the promise of new medical discovery closer within reach for patients. Emmes Group was founded as Emmes more than 47 years ago, becoming one of the primary clinical research providers to the US government before expanding into public-private partnerships and commercial biopharma. Emmes has built industry leading capabilities in cell and gene therapy, vaccines and infectious diseases, ophthalmology, rare diseases, and neuroscience.

We believe the work we do will have a direct impact on patients' lives and act accordingly. We strive to build a collaborative culture at the intersection of being a performance and people driven company. We're looking for talented professionals eager to help advance clinical research as we work to embed innovation into the fabric of our company. If you share our motivations and passion in research, come join us!

Primary Purpose

Leads collaborations with clinical investigators to determine study design, contributes to protocol development, authors statistical analysis plans, performs statistical analysis, makes statistical inference and writes and presents reports summarizing findings including publications in peer reviewed journals. Manages statistical activities for a clinical study or platform of clinical studies.

Responsibilities
  • Provides sound strategic, scientific and statistical input to support client's research projects.
  • Serves as the lead Biostatistician on one or more study projects.
  • May supervise Biostatisticians, Associate Biostatisticians and SAS programmers (all levels) and direct their work on clinical research studies.
  • Leads the project team's development of study analysis plans and statistical programs to perform analyses and display study data.
  • Keeps abreast with current statistical and medical literature to ensure that sound methodologies are adopted.
  • Fosters innovation in Biostatistics that will continuously enhance current statistical knowledge and practices.
  • Ensures the scientific integrity of the research project and the accuracy of the reported results.
  • Performs sample size calculation and provides leadership in the statistical design of research projects.
  • Reviews protocols and case report forms to ensure that protocol objectives are met, and standards are maintained.
  • Develops study assignment allocation schemas along with appropriate documentation.
  • Leads the development of the methods and results sections of clinical study reports and scientific publications.
  • Represents EMMES on behalf of clients at regulatory meetings.
  • Participate in the development and updating of Standard Operating Procedures.
  • Performs other duties as assigned
  • Complies with all policies and standards
Qualifications
  • PhD or MS in Biostatistics, statistics, epidemiology or related field required
  • 4-6 years of related experience is expected but not required for the position.
  • 1-3 years Demonstrated proficiency with statistical methods and applications in clinical research required.
  • 1-3 years Strong programming skills in SAS and/or R required.

Why work at Emmes?

At Emmes, your actions and hard work will have a direct impact on public health initiatives, both globally and in our local communities with opportunities for volunteerism through our  Emmes Cares  community engagement program.   We offer a competitive benefits package focused on the health and needs of our growing workforce, including:

  • Flexible Approved Time Off
  • Tuition Reimbursement
  • 401k Retirement Plan
  • Work From Home Anywhere in the US
  • Maternal/Paternal Leave
  • Casual Dress Code & Work Environment

CONNECT WITH US!

Follow us on Twitter - @EmmesCRO

Find us on LinkedIn - Emmes

The Emmes Company, LLC is an equal opportunity employer and does not discriminate in its selection and employment practices. All qualified applicants will receive consideration for employment without regard to disability or protected veteran status.

#LI-Remote 

Employment Type: FULL_TIME
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About Emmes

Sourced by ZipRecruiter

Industry

Scientific research and development services

Company size

201 - 500 Employees

Headquarters location

Rockville, MD, US

Year founded

1977

Social media

Twitter

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