1

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

Be Seen First

This position offers an exciting opportunity to work at the forefront of clinical development in a ... Proven supervising experience in a clinical research setting or related healthcare environment

We are seeking a Clinical Research Coordinator to provide comprehensive clinical research ... Position may be eligible for a discretionary variable incentive bonus About Guidehouse Guidehouse ...

Be Seen First

This position offers an exciting opportunity to work at the forefront of clinical development in a ... Proven supervising experience in a clinical research setting or related healthcare environment

Clinical Research Coordinator

Bethesda, MD · On-site

$26 - $34.50/hr

The total hourly pay for this non-exempt position is $30.00 for up to 40 hours per week. This rate ... Supports clinical staff develop, implement and maintain clinical research data files and materials ...

Showing results 21-40

Clinical Research Position information

See Reston, VA salary details

$51K

$111.7K

$196.6K

How much do clinical research position jobs pay per year?

As of Aug 22, 2026, the average yearly pay for clinical research position 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 a clinical research position?

A clinical research position typically involves planning, coordinating, and conducting research studies that test new medical treatments, drugs, or devices in human participants. Professionals in these roles may work in hospitals, universities, or pharmaceutical companies to ensure that studies are ethically conducted and compliant with regulatory standards. Their responsibilities can include recruiting participants, collecting and analyzing data, and maintaining documentation. These positions are vital for advancing medical knowledge and improving patient care.

How does a clinical research professional typically collaborate with healthcare providers and regulatory teams during a clinical trial?

Clinical research professionals work closely with healthcare providers, such as physicians and nurses, to ensure that study protocols are followed and that patient safety is maintained throughout the trial. They also interact regularly with regulatory teams to ensure compliance with local and international regulations, assisting with the preparation and submission of necessary documentation. Effective communication and collaboration are essential, as clinical research professionals act as a bridge between the research team, clinical staff, and regulatory authorities to facilitate smooth trial execution.

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

To thrive in a Clinical Research Position, you need a solid understanding of clinical trial protocols, regulatory compliance, and data analysis, typically supported by a degree in life sciences or a related field. Familiarity with electronic data capture systems, clinical trial management software (CTMS), and certifications such as Good Clinical Practice (GCP) are commonly required. Strong attention to detail, effective communication, and the ability to collaborate across multidisciplinary teams help professionals excel in this field. These skills are critical for ensuring accurate data collection, regulatory adherence, and successful execution of clinical studies.

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

AspectClinical Research PositionClinical Research Coordinator
CredentialsVaries; often includes degrees in health sciences, certifications like CCRPTypically requires a bachelor's degree in health or life sciences, certification preferred
Work EnvironmentResearch labs, pharmaceutical companies, academic institutionsHospitals, clinics, research sites
Employer & Industry UsageUsed across biotech, pharma, academiaCommonly employed in clinical trial sites and hospitals
Job FocusDesigning, managing, and analyzing clinical studiesOverseeing daily trial activities, patient coordination

The Clinical Research Position generally involves higher-level responsibilities like study design and data analysis, often requiring advanced certifications. The Clinical Research Coordinator focuses on managing daily trial operations and patient interactions at research sites. Both roles are essential in clinical research but differ in scope and responsibilities.

What do you do as a clinical research position?

A clinical research position involves designing, conducting, and managing clinical trials to evaluate the safety and effectiveness of medical treatments or devices. Professionals in this role collect and analyze data, ensure compliance with regulatory standards, and often work with healthcare teams and research protocols. Strong organizational skills and knowledge of Good Clinical Practice (GCP) are essential for success in this field.

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

To qualify for a clinical research position, candidates typically need a bachelor's degree in a health-related field such as biology, nursing, or pharmacy. Relevant skills include knowledge of Good Clinical Practice (GCP), attention to detail, and experience with data management or clinical trial protocols; some roles may require certification like the Certified Clinical Research Professional (CCRP).

What job categories do people searching Clinical Research Position jobs in Reston, VA look for?

The top searched job categories for Clinical Research Position jobs in Reston, VA are:

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

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

Clinical Research Coordinator

CENTER FOR DERMATOLOGY

Washington, DC • On-site

$62K - $82K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 11 days ago

Be Seen First

After you apply to this job, you can share why you’re interested to jump to the top of the candidate list.


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.