1

Clinical Trials Assistant Jobs in Reston, VA (NOW HIRING)

Clinical Research Coordinator

Bethesda, MD

$26 - $34.50/hr

Dependent Care Assistant Program (DCAP) * Transportation Reimbursement Account (TRN) Position ... Demonstrated experience supporting clinical trials from startup through closeout Deliverables

Clinical Research Coordinator

Bethesda, MD

$26 - $34.50/hr

Dependent Care Assistant Program (DCAP) * Transportation Reimbursement Account (TRN) Position ... Demonstrated experience supporting clinical trials from startup through closeout Deliverables

Clinical Research Coordinator

Bethesda, MD · On-site

$26 - $34.50/hr

Dependent Care Assistant Program (DCAP) * Transportation Reimbursement Account (TRN) Position ... Demonstrated experience supporting clinical trials from startup through closeout Deliverables

... trials conducted within the National Cancer Institute (NCI). This is a full-time, on-site role in ... Coordinate multiple clinical research studies simultaneously. * Assist with onboarding activities ...

... trials conducted within the National Cancer Institute (NCI). This is a full-time, on-site role in ... Coordinate multiple clinical research studies simultaneously. * Assist with onboarding activities ...

Clinical Research Coordinator

Bethesda, MD · On-site

$26 - $34.50/hr

IRB Submissions: Assist with the preparation and submission of regulatory documentation to ... Direct experience supporting oncology clinical trials and clinical research operations.

Clinical Program Manager

Bethesda, MD · On-site

$85K - $141K/yr

Coordinate operational and startup activities for clinical trials, including feasibility ... guidelines. * Assist with financial management activities, including budget development ...

Coordinate operational and startup activities for clinical trials, including feasibility ... guidelines. * Assist with financial management activities, including budget development ...

next page

Showing results 1-20

Clinical Trials Assistant information

See Reston, VA salary details

$12

$21

$30

How much do clinical trials assistant jobs pay per hour?

As of Aug 8, 2026, the average hourly pay for clinical trials assistant in Reston, VA is $21.05, according to ZipRecruiter salary data. Most workers in this role earn between $17.26 and $24.28 per hour, depending on experience, location, and employer.

What is a clinical trials assistant?

Clinical Trials Assistants (CTAs) are professionals who support the planning, coordination, and administration of clinical trials, which are research studies that evaluate the safety and effectiveness of medical treatments or interventions. They handle tasks such as maintaining trial documentation, assisting with regulatory submissions, scheduling meetings, and ensuring data accuracy. CTAs play a crucial role in helping clinical research teams comply with protocols and regulatory requirements, making the clinical trial process run smoothly and efficiently.

How do I become a clinical trials assistant?

To become a clinical trials assistant, candidates typically need a high school diploma or equivalent, with some roles preferring post-secondary education in health or science fields. Relevant skills include attention to detail, organization, and familiarity with clinical trial protocols; certification in Good Clinical Practice (GCP) can be beneficial. Entry-level positions often require basic computer skills and the ability to work in a team environment.

How to become a clinical trials assistant?

To become a clinical trials assistant, candidates typically need a high school diploma or equivalent, with some roles preferring post-secondary education in health or science fields. Relevant skills include attention to detail, organization, and familiarity with clinical trial protocols and documentation. Gaining experience through internships or entry-level positions in healthcare or research settings can also improve job prospects.

What are some typical challenges a clinical trials assistant faces during a study, and how can they be managed?

Clinical Trials Assistants often encounter challenges such as managing large volumes of documentation, ensuring timely data entry, and coordinating communication among multiple stakeholders. Staying organized and using established tracking systems can help manage documents efficiently. Proactive communication and regular check-ins with team members—such as study coordinators and data managers—are key to resolving issues quickly and maintaining study timelines. Embracing good time management practices and seeking mentorship from senior staff can further ease these common challenges.

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

AspectClinical Trials AssistantClinical Research Coordinator
CredentialsHigh school diploma or equivalent; some roles may require certificationBachelor’s degree in health sciences or related field; often requires certification
Work EnvironmentResearch sites, hospitals, clinics, pharmaceutical companiesResearch sites, hospitals, clinics, pharmaceutical companies
ResponsibilitiesAssist with data entry, document management, and trial logisticsOversee trial processes, patient recruitment, data collection, and compliance
Industry UsageCommonly used in clinical trial support rolesMore involved in trial management and coordination

While both roles support clinical trials, Clinical Trials Assistants focus on administrative and logistical tasks, whereas Clinical Research Coordinators handle more comprehensive trial management, patient interactions, and compliance activities.

What are the key skills and qualifications needed to thrive as a clinical trials assistant?

To thrive as a Clinical Trials Assistant, you need a solid understanding of clinical research processes, regulatory guidelines, and attention to detail, often supported by a degree in life sciences. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and Good Clinical Practice (GCP) certification is typically required. Strong organizational skills, effective communication, and the ability to multitask make candidates stand out in this role. These skills are essential for ensuring compliance, accurate documentation, and the smooth execution of clinical studies.
What are the most commonly searched types of Clinical Trials jobs in Reston, VA? The most popular types of Clinical Trials jobs in Reston, VA are:
What are popular job titles related to Clinical Trials Assistant jobs in Reston, VA? For Clinical Trials Assistant jobs in Reston, VA, the most frequently searched job titles are:
What job categories do people searching Clinical Trials Assistant jobs in Reston, VA look for? The top searched job categories for Clinical Trials Assistant jobs in Reston, VA are:
What cities near Reston, VA are hiring for Clinical Trials Assistant jobs? Cities near Reston, VA with the most Clinical Trials Assistant job openings:
Infographic showing various Clinical Trials Assistant job openings in Reston, VA as of August 2026, with employment types broken down into 2% As Needed, 70% Full Time, 21% Part Time, and 7% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $43,778 per year, or $21 per hour.

Biostatistics and Clinical Trials Advisor

Booz Allen Hamilton

Washington, DC • On-site, Remote

Full-time

Medical, Life, Retirement, PTO

Posted 11 days ago


Booz Allen Hamilton rating

8.9

Company rating: 8.9 out of 10

Based on 49 frontline employees who took The Breakroom Quiz

9th of 72 rated business consultants


Job description

Biostatistics and Clinical Trials Advisor

The Opportunity:

To achieve an organization's mission, leaders need strong team members who can create processes, communicate requirements, and develop innovative solutions throughout the execution of the mission. Whether completing an immediate task, recognizing a process gap, recommending a solution, or flexing to support an immerging requirement, our clients need a consultant who can help manage operations while managing responses to external inquiries in a timely manner. That is why we need you, an experienced Biostatistics and Clinical Trials Advisor, to provide technical expertise and project development for emerging opportunities within healthcare.

As part of our team, you'll serve as a strategic technical consultant to the Advanced Research Projects Agency for Health (ARPA-H), helping conceptualize, create, and execute advanced government-funded research and development programs to accelerate better health outcomes for everyone. Work with world-class scientists and engineers to support the development of high-impact solutions to society's most challenging health problems. Leverage technical expertise to provide strategic assessments of new technologies in support to senior ARPA-H decision makers. Maintain responsibility for producing and presenting findings and recommendations to a team of colleagues and clients on the feasibility and potential impact of future research programs, assisting with the management of current programs, and facilitating commercialization of successfully developed technologies.

You'll serve as a Biostatistics and Clinical Trials Advisor helping clients to develop stakeholder management strategies, establish new business processes, and complete research and analysis to determine viable solutions. You will be responsible for managing incoming requirements, facilitating engagements within offices and across the Agency, and being readily available to shift your focus to fulfill emerging client requests. Your attention to detail, flexibility, communication skills, understanding of the client's mission, and problem-solving will enable the mission's success.

What You'll Work On:

  • Support strategy development and program execution for biostatistics, clinical trials, artificial intelligence/machine learning for clinical trials, and computational modeling initiatives

  • Offer deep technical insight into the design and evaluation of clinical trials, including innovative approaches such as adaptive, platform, digital twins, or in silico clinical trial simulations

  • Advise on quantitative and statistical modeling for pharmacology, including Bayesian, frequentist, and empirical modeling approaches

  • Evaluate the credibility and standards for computational and physicsbased models for drugs, biologics, and advanced therapeutics, such as Quantitative Systems Pharmacology, Pharmacokinetic/Pharmacodynamic, or digital twin

  • Coordinate with federal stakeholders and other interagency partners to support the development, evaluation, and transition of new drug clinical trial projects

  • Evaluate the conceptual and technical soundness of research programs spanning biostatistics, clinical trials, artificial intelligence/machine learning for clinical trials, and computational modeling

  • Assist in defining program goals, technical milestones, budgets, and performer expectations for high-impact scientific initiatives; conduct technical reviews of performer progress to ensure alignment with ARPA-H objectives

  • Interact with clients, government officials, and other executives in various sectors

Join us. The world can't wait.

You Have:

  • 3+ years of experience building physics-based and mechanistic models for drugs or biologics

  • 1+ years of experience supporting new drug clinical trials of any phase for products regulated by FDA CDER or CBER, such as drugs, biologics, or advanced therapies

  • Experience with Bayesian, frequentist, and empirical methods

  • Experience supporting and advising government leadership or federal research programs

  • Knowledge of biostatistics and statistical modeling

  • Knowledge of clinical trial design

  • Ability to manage budgets, technical milestones, and multidisciplinary research efforts across multi-site or multi-performer programs

  • Doctorate degree in Biostatistics, Bioinformatics, Computational Biology, Epidemiology, or a Biomedical or Health Sciences field

Nice If You Have:

  • Experience with disease- or patient-specific digital twin models

  • Experience with in silico clinical trial simulations, specifically clinical trial optimization via in silico simulations

  • Experience with synthetic data generation to augment real control patients in clinical trials

  • Experience in the development or evaluation of artificial intelligence/machine learning approaches

  • Experience with innovative clinical trial design approaches such as adaptive and platform trial designs

  • Experience with assessing the credibility or development of standards for computational and physics-based models such as Quantitative Systems Pharmacology (QSP) and Pharmacokinetic/Pharmacodynamic (PK/PD) models

  • Experience operating within a government environment and supporting senior federal leaders

  • Ability to manage multiple priorities at once

  • Possession of excellent communication skills

Compensation

At Booz Allen, we celebrate your contributions, provide you with opportunities and choices, and support your total well-being. Our offerings include health, life, disability, financial, and retirement benefits, as well as paid leave, professional development, tuition assistance, work-life programs, and dependent care. Our recognition awards program acknowledges employees for exceptional performance and superior demonstration of our values. Full-time and part-time employees working at least 20 hours a week on a regular basis are eligible to participate in Booz Allen's benefit programs. Individuals that do not meet the threshold are only eligible for select offerings, not inclusive of health benefits. We encourage you to learn more about our total benefits by visiting the Resource page on our Careers site and reviewing Our Employee Benefits page.

Salary at Booz Allen is determined by various factors, including but not limited to location, the individual's particular combination of education, knowledge, skills, competencies, and experience, as well as contract-specific affordability and organizational requirements. The projected compensation range for this position is $86,800.00 to $198,000.00 (annualized USD). The estimate displayed represents the typical salary range for this position and is just one component of Booz Allen's total compensation package for employees. This posting will close within 90 days from the Posting Date.

Identity Statement

As part of the hiring process, we will ask you to complete an identity verification process that leverages advanced biometrics and artificial intelligence to ensure authenticity and protect against identity fraud. You are expected to be on camera during interviews and assessments. We reserve the right to take your picture to verify your identity and prevent fraud.

Candidate AI Usage Policy

AI is a part of our daily work at Booz Allen, and we are committed to the responsible and ethical use of AI tools. However, we want to ensure a fair candidate process based on your own skills and knowledge. As part of this commitment, the use of artificial intelligence (AI) or other tools to assist with responses during interviews (whether in-person or virtual) is prohibited unless permission is explicitly provided.

Work Model
Our people-first culture prioritizes the benefits of collaboration, whether it occurs in person or virtually. To support engagement and effective communication, employees working virtually are generally expected to have their cameras on during meetings.

  • Remote: If this position is listed as remote, there may still be occasions when you are required to work in person at a Booz Allen or customer facility.

  • Hybrid: If this position is listed as hybrid, you will be expected to work from a Booz Allen facility frequently, in alignment with leadership expectations and the needs of the role. You may also be required to work from or visit a customer facility.

  • Onsite: If this position is listed as onsite, work will primarily be performed at a Booz Allen office or customer facility, where employees will collaborate directly with colleagues and customers as required by the role.

Commitment to Non-Discrimination

All qualified applicants will receive consideration for employment without regard to disability, status as a protected veteran or any other status protected by applicable federal, state, local, or international law.


What Booz Allen Hamilton employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom


Booz Allen Hamilton logo

About Booz Allen Hamilton

Sourced by ZipRecruiter

Booz Allen Hamilton is a leading provider of management and technology consulting services to the US government in defense, intelligence, and civil markets. Headquartered in McLean, Virginia, the firm also serves major corporations, institutions, and not-for-profit organizations. Founded in 1914 by Edwin G. Booz, the company has a long-standing tradition of helping clients achieve success by delivering a wide range of consulting services that include strategic planning, human capital and learning, communication, systems development, and others. The company's mission is to empower people to change the world, and it has a reputation for maintaining the highest standards of integrity and-excellence.

Industry

It services

Company size

10,000+ Employees

Headquarters location

McLean, VA, US

Year founded

1914