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

CENTER FOR DERMATOLOGY

Be Seen First

Clinical Research Coordinator

Washington, DC · On-site

$62K - $82K/yr

Job Overview We are seeking a highly motivated and detail-oriented Clinical Research Coordinator to join our dynamic research team. In this vital role, you will oversee the planning, coordination ...

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Howard University

Research Assistant- HIAS

Washington, DC · On-site

$50K - $55K/yr

The Research Assistant conducts research across HIAS's programmatic areas, including HIAS research projects, the Director's research projects, and research for The Emancipator. The Research Assistant ...

Howard University

Research Assistant

Washington, DC · On-site

$20/hr

The position may span basic science, clinical, translational, or population-based research ... PRINCIPAL ACCOUNTABILITIES: * Assist in the design and execution of research experiments, surveys ...

Howard University

Research Assistant

Washington, DC · On-site

$40K - $50K/yr

The Kidane Lab at Howard University College of Medicine is seeking a full-time Research Assistant/Lab Manager to study DNA repair, tumor immunology, and cancer biology. The position is available ...

Howard

Research Assistant

Washington, DC

$40K - $50K/yr

The Kidane Lab at Howard University College of Medicine is seeking a full-time Research Assistant/Lab Manager to study DNA repair, tumor immunology, and cancer biology. The position is available ...

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How much do clinical research assistant jobs pay per hour?

As of Aug 12, 2026, the average hourly pay for clinical research assistant in Reston, VA is $23.63, according to ZipRecruiter salary data. Most workers in this role earn between $18.03 and $27.02 per hour, depending on experience, location, and employer.

What is a clinical research assistant?

Clinical Research Assistants are professionals who support clinical research studies by performing a range of administrative and research-related tasks. They help collect and manage data, assist with patient recruitment, prepare study materials, and ensure compliance with research protocols and regulations. Their work is crucial in advancing medical knowledge and ensuring that clinical trials run smoothly and ethically. Clinical Research Assistants often work under the supervision of principal investigators or clinical research coordinators in hospitals, universities, or pharmaceutical companies.

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

To thrive as a Clinical Research Assistant, you need a bachelor’s degree in a life science or health-related field, attention to detail, and strong organizational skills. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and good clinical practice (GCP) certification are typically required. Excellent communication, teamwork, and problem-solving abilities help you excel in coordinating with research teams and participants. These skills ensure accurate data collection, regulatory compliance, and the smooth execution of clinical studies.

What does a clinical research assistant do?

A clinical research assistant—or clinical research associate (CRA)—helps lead researchers during clinical trials for new drugs and medical devices. As a clinical research assistant, your responsibilities include preparing the laboratory, processing volunteers, taking biological samples or vital signs, and organizing data. You may also be required to set up and clean work areas. Your job is to assist the researchers in any way possible, helping them conduct sound, ethical, and scientifically accurate research.

What are some common challenges clinical research assistants face when coordinating multiple studies simultaneously?

Clinical Research Assistants often manage several studies at once, which can lead to challenges in balancing competing deadlines, maintaining accurate documentation, and ensuring compliance with complex protocols. Effective time management and organizational skills are crucial to handle overlapping tasks such as scheduling patient visits, collecting data, and preparing regulatory submissions. Collaborating closely with principal investigators, coordinators, and other team members helps distribute the workload and maintain research quality. Developing strong communication habits and utilizing digital tracking tools can further streamline workflow and reduce errors.

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

AspectClinical Research AssistantClinical Research Coordinator
CredentialsTypically requires a bachelor's degree in health sciences or related field; certifications like CCRP are a plusRequires a bachelor's degree; certifications such as CCRP or CCRC are common
Work EnvironmentAssists in data collection, patient scheduling, and administrative tasks in clinical trial settingsManages study protocols, patient recruitment, and regulatory compliance in clinical trial sites
Employer & IndustryHospitals, research institutions, pharmaceutical companiesHospitals, research centers, pharmaceutical companies

Both roles support clinical research but differ in responsibilities. Clinical Research Assistants focus on data collection and administrative tasks, while Clinical Research Coordinators oversee study management and patient interactions. Understanding these differences helps in choosing the right career path or job search focus.

Can you be a clinical research assistant with no experience?

Clinical research assistants often start with little or no experience, as entry-level positions may provide on-the-job training. Relevant skills such as attention to detail, organizational ability, and familiarity with medical or research environments can help candidates qualify, but some employers may prefer candidates with related coursework or certifications. Gaining experience through internships or volunteering can also improve prospects for entry-level applicants.
More about Clinical Research Assistant jobs
What are the most commonly searched types of Clinical Research jobs in Reston, VA? The most popular types of Clinical Research jobs in Reston, VA are:
What are popular job titles related to Clinical Research Assistant jobs in Reston, VA? For Clinical Research Assistant jobs in Reston, VA, the most frequently searched job titles are:
What job categories do people searching Clinical Research Assistant jobs in Reston, VA look for? The top searched job categories for Clinical Research Assistant jobs in Reston, VA are:
What cities near Reston, VA are hiring for Clinical Research Assistant jobs? Cities near Reston, VA with the most Clinical Research Assistant job openings:
Clinical Research Assistant jobs near you
Infographic showing various Clinical Research Assistant job openings in Reston, VA as of August 2026, with employment types broken down into 2% As Needed, 73% Full Time, 19% Part Time, and 6% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $49,147 per year, or $23.6 per hour.

Clinical Research Coordinator

CENTER FOR DERMATOLOGY

Washington, DC • On-site

$62K - $82K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted yesterday

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Job description

Job Overview
We are seeking a highly motivated and detail-oriented Clinical Research Coordinator to join our dynamic research team. In this vital role, you will oversee the planning, coordination, and execution of clinical trials, ensuring compliance with regulatory standards and maintaining the highest quality of data collection. Your expertise will help advance innovative medical research and improve patient outcomes. We are in search of a candidate who is extremely strong on regulatory affairs. This position offers an exciting opportunity to work at the forefront of clinical development in a fast-paced, collaborative environment. The candidate must be able to work in both our Washington, DC 20037 and Annapolis, MD, 21401

Duties

  • Coordinate and manage all aspects of clinical trials, including patient recruitment, scheduling, and follow-up procedures
  • Ensure adherence to FDA regulations, ICH Good Clinical Practice (GCP), and HIPAA guidelines to maintain compliance throughout all trial phases
  • Review and verify study documentation for accuracy, completeness, and regulatory compliance
  • Monitor patient safety by conducting vital signs assessments, blood sampling (phlebotomy), and tracking adverse events
  • Manage data collection, entry, and management using electronic medical record (EMR) systems and adhere to CDISC standards for data consistency
  • Supervise clinical staff involved in trial activities, providing guidance on protocol adherence and documentation review
  • Oversee clinical laboratory procedures and collaborate with laboratory personnel to ensure accurate sample handling and analysis skills are maintained
  • Conduct patient monitoring visits, review medical histories, and ensure proper documentation of clinical findings
  • Maintain detailed records of trial activities, prepare reports for regulatory submissions, and support audit readiness efforts

Experience

  • Proven supervising experience in a clinical research setting or related healthcare environment
  • Extensive knowledge of clinical trials management, including protocol development and regulatory compliance
  • Strong understanding of medical terminology, blood sampling techniques, vital signs measurement, and clinical laboratory procedures
  • Experience with data management systems, EMR platforms, and statistical software used in clinical research analysis
  • Familiarity with FDA regulations, ICH GCP guidelines, HIPAA privacy rules, and CDISC standards for data interchange
  • Background in nursing or phlebotomy is highly desirable; relevant certifications such as an ICH GCP certificate from a valid issuer for CRC are preferred
  • Demonstrated ability to coordinate multiple tasks efficiently while maintaining attention to detail in a fast-paced environment

Join us to make a meaningful impact on healthcare innovation! We are committed to fostering an inclusive environment where your skills can thrive. This paid position offers comprehensive training opportunities and the chance to develop your expertise in clinical research while supporting groundbreaking medical advancements.