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Clinical Research Jobs in Reston, VA (NOW HIRING)

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Clinical Research Coordinator

Washington, DC · On-site

$62K - $82K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

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 ...

Be Seen First

Clinical Research Coordinator

Washington, DC · On-site

$62K - $82K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

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 ...

Clinical Research Nurse

Washington, DC · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Requirements Job Overview The Clinical Research nurse, Lombardi Cancer Center - Georgetown University, is a position in the benign Hematology clinical research program. Under the guidance and ...

Clinical Research Nurse

Washington, DC · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Requirements Job Overview The Clinical Research nurse, Lombardi Cancer Center - Georgetown University, is a position in the benign Hematology clinical research program. Under the guidance and ...

Clinical Research Nurse

Washington, DC · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Requirements Job Overview The Clinical Research nurse, Lombardi Cancer Center - Georgetown University, is a position in the benign Hematology clinical research program. Under the guidance and ...

Clinical Research Coordinator

Leesburg, VA · On-site

$31 - $38/hr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

At Virginia Heart, we are looking for a professional Clinical Research Coordinator will plan, direct, evaluate and analyze clinical research trials related to cardiac drug and device trials.

Clinical Research Coordinator

Bethesda, MD · On-site

$26 - $34.50/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Concentric Methods is seeking an experienced Clinical Research Coordinator to independently provide support services to the NIH. The total hourly pay for this non-exempt position is $30.00 for up to ...

Clinical Research Coordinator

Washington, DC · On-site

$20.16 - $31.30/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Requirements Job Overview The Research Coordinator for the Clinical Research Unit (CRU) at Georgetown University will support clinical research nurses in the care of research and standard of care ...

Clinical Research Coordinator

Washington, DC · On-site

$27.50 - $36.75/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Requirements Job Overview The Clinical Research Coordinator 2 (CRC2) is responsible for managing and coordinating 7 out of approximately 55 ongoing clinical trials, Phases I-IV, in the Dept. of ...

Showing results 21-40

Clinical Research information

See Reston, VA salary details

$51K

$111.7K

$196.6K

How much do clinical research jobs pay per year?

As of Aug 20, 2026, the average yearly pay for clinical research in Reston, VA is $111,668.00, according to ZipRecruiter salary data. Most workers in this role earn between $84,300.00 and $127,400.00 per year, depending on experience, location, and employer.

What is clinical research?

Clinical research is a branch of healthcare science that focuses on studying human health and illness through clinical trials and observational studies. It aims to improve medical knowledge by testing new treatments, drugs, medical devices, or interventions in controlled environments. Clinical research professionals design, conduct, and monitor studies to ensure that data is accurate and that participant safety and ethical standards are maintained. The results of clinical research can lead to new therapies, improved patient care, and informed healthcare policies.

What are different clinical research jobs?

Some of the different types of clinical research jobs include clinical research associates, coordinators, data managers, clinical nurses, research scientists, and biostatisticians. There are also administrative, managerial, and recruitment positions. As a research associate, you monitor the clinical trials and the people administering them, such as clinical nurses and research coordinators who work under the direction of the principal investigator. As a biostatistician, your duties are to collect data about the study and analyze the results to determine if the medication or treatment shows statistically significant effects on participants.

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

To thrive in Clinical Research, you need a strong background in life sciences, data analysis, and regulatory compliance, often supported by a relevant degree and experience in clinical trials. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and certifications like GCP (Good Clinical Practice) are commonly required. Attention to detail, strong organizational skills, and effective communication make candidates stand out in this field. These skills ensure the integrity of research data, regulatory adherence, and successful collaboration among cross-functional teams.

What are some typical challenges faced by professionals in clinical research, and how can they be managed?

Clinical research professionals often face challenges such as strict regulatory compliance, tight timelines, and coordination among multidisciplinary teams. Managing large volumes of data and ensuring participant safety are also key concerns. Staying organized, maintaining open communication with team members, and keeping updated on regulatory changes can help professionals navigate these challenges effectively. It's also helpful to develop strong project management skills and to build collaborative relationships with investigators, sponsors, and regulatory bodies.

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

AspectClinical ResearchClinical Data Coordinator
Required CredentialsTypically a bachelor's degree in health sciences, life sciences, or related field; certifications like CCR or CCRA are commonOften a bachelor's degree in health or data management; certifications like CDMP or CCRC may be preferred
Work EnvironmentResearch sites, pharmaceutical companies, CROs, hospitalsClinical trial sites, hospitals, research organizations
Job FocusDesigning, managing, and overseeing clinical trialsManaging and ensuring accuracy of clinical trial data

Clinical Research involves overseeing entire clinical trials, including protocol development and compliance, while Clinical Data Coordinators focus on collecting, managing, and ensuring the quality of trial data. Both roles are essential in the clinical research process but differ in scope and responsibilities.

How do you become a clinical researcher?

To become a clinical researcher, typically a bachelor's degree in a health-related field such as biology, nursing, or medicine is required, followed by relevant experience or advanced education like a master's or PhD. Certification in clinical research, such as the Certified Clinical Research Professional (CCRP), can enhance job prospects. Strong analytical skills, knowledge of regulatory guidelines, and familiarity with research tools are also important.

Is clinical research a good career path?

Clinical research is a viable career that involves managing and conducting trials to test new medical treatments and drugs. It requires strong organizational skills, knowledge of regulatory guidelines, and often a background in healthcare or life sciences. The field offers opportunities for advancement and specialization, with roles in research coordination, data management, and regulatory affairs.

What do you do in a clinical research job?

A clinical research job involves designing, conducting, and managing studies to evaluate the safety and effectiveness of medical treatments or devices. Professionals in this field collect and analyze data, ensure compliance with regulatory standards, and often work with clinical trial participants, using tools like electronic data capture systems. Strong attention to detail, knowledge of Good Clinical Practice (GCP), and relevant certifications are important for success.

What qualifications do you need to be a clinical research professional?

A clinical research professional typically needs a bachelor's degree in a health-related field such as biology, nursing, or pharmacy. Relevant certifications, like the Certified Clinical Research Professional (CCRP), and knowledge of Good Clinical Practice (GCP) guidelines are often required. Strong organizational skills and familiarity with clinical trial management systems are also important.

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 jobs in Reston, VA?

For Clinical Research jobs in Reston, VA, the most frequently searched job titles are:

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

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

Infographic showing various Clinical Research job openings in Reston, VA as of August 2026, with employment types broken down into 3% As Needed, 73% Full Time, 16% Part Time, and 8% Contract. Highlights an 93% Physical, 2% Hybrid, and 5% Remote job distribution, with an average salary of $111,668 per year, or $53.7 per hour.

Clinical Research Coordinator

CENTER FOR DERMATOLOGY

Washington, DC • On-site

$62K - $82K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 9 days ago

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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.