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Clinical Research Organization Jobs in Reston, VA

Clinical Research Coordinator

Bethesda, MD · On-site

$26 - $34.50/hr

We work with some of the top research organizations and facilities in the country including multiple institutes at the National Institutes of Health (NIH). Axle is seeking a Clinical Research ...

Clinical Research Coordinator

Bethesda, MD · On-site

$26 - $34.50/hr

We work with some of the top research organizations and facilities in the country including multiple institutes at the National Institutes of Health (NIH). Axle is seeking a Clinical Research ...

We are seeking a Clinical Research Coordinator to provide comprehensive clinical research ... Strong organizational and project coordination skills * Effective communication skills The annual ...

We are seeking a Clinical Research Coordinator to provide comprehensive clinical research ... Strong organizational and project coordination skills * Effective communication skills The annual ...

Clinical Research Coordinator

Bethesda, MD · On-site

$26 - $34.50/hr

Concentric Methods is seeking an experienced Clinical Research Coordinator to independently provide ... Strong organizational and time management skills. Excellent interpersonal and communication skills ...

At Virginia Heart, we are looking for a professional Clinical Research Coordinator will plan ... Strong organizational and analytical skills required * In depth knowledge of Good Clinical Practice ...

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Clinical Research Organization information

See Reston, VA salary details

$51K

$111.7K

$196.6K

How much do clinical research organization jobs pay per year?

As of Aug 20, 2026, the average yearly pay for clinical research organization 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 organization?

A Clinical Research Organization (CRO) job involves supporting pharmaceutical, biotechnology, and medical device companies in conducting clinical trials and research. CRO employees help with tasks such as regulatory compliance, data management, patient recruitment, and trial monitoring. These roles ensure that new treatments and medical advancements are tested safely and efficiently. Positions within a CRO can range from clinical research associates to data analysts and project managers. Working in a CRO offers opportunities to contribute to drug development while collaborating with sponsors and regulatory agencies.

What are the key skills and qualifications needed to thrive in a clinical research organization position?

To excel within a Clinical Research Organization, individuals typically need a background in life sciences, strong project management skills, and experience with clinical trial protocols and regulatory requirements. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and certifications such as GCP (Good Clinical Practice) are highly valued. Excellent organizational skills, attention to detail, and effective communication enhance collaboration across multidisciplinary teams and with sponsors. These skills are crucial for maintaining compliance, ensuring data integrity, and delivering successful clinical research projects.

What kinds of career growth opportunities are available when working for a clinical research organization?

Clinical Research Organizations (CROs) offer a range of career advancement opportunities across clinical operations, data management, regulatory affairs, and project management. Employees often start in entry-level roles such as Clinical Research Associate (CRA) or Data Coordinator and can progress to senior, management, or specialist positions with experience and further training. CROs frequently support professional development through training programs and encourage movement between departments, allowing for a diverse and rewarding career path. Teamwork, adaptability, and a proactive approach to skill-building are key to seizing growth opportunities in this dynamic industry.

What are the most commonly searched types of Clinical Research Organization jobs in Reston, VA?

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

What are popular job titles related to Clinical Research Organization jobs in Reston, VA?

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

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

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

Infographic showing various Clinical Research Organization job openings in Reston, VA as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 14% Part Time, and 4% Contract. Highlights an 90% Physical, 3% Hybrid, and 7% Remote job distribution, with an average salary of $111,668 per year, or $53.7 per hour.

Temporary

Medical, Dental, Vision, Retirement, PTO

Posted yesterday

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Velocity Clinical Research rating

7.3

Company rating: 7.3 out of 10

Based on 5 frontline employees who took The Breakroom Quiz

75th of 120 rated laboratories


Job description

Velocity Clinical Research is an owned and integrated research site organization, providing excellence in patient care, high quality data and fully integrated research sites. At Velocity, we align our values and behaviors to give our employees the best chance of delivering on our brand promise: to bring innovative medical treatments to patients. We are committed to making clinical trials succeed by generating high quality data from as many patients as possible, as quickly as possible while providing exemplary patient care at every step.

As an employee of Velocity, you are the most integral part of our mission. For talented candidates who perform at a high level, Velocity will invest to support career advancement and reward performance. Whether you are new to clinical research or are an industry veteran, we invite you to apply to Velocity.

Benefits include medical, dental and vision insurance, paid time off and company holidays, 401(k) retirement plan with company-match, and an annual incentive program.

Summary:

The Clinical Research Assistant assists the Clinical Operations Team in a multi-functional capacity to carry out all assigned tasks associated with the collection, documentation, and maintenance of clinical data including phlebotomy/laboratory, data entry and administrative responsibilities.


Duties/Responsibilities:

  • Assist in the conduct of clinical trials in accordance with the study protocol, GCP, ICH Guidelines, and Velocity’s SOPs
  • Perform venipuncture, capillary puncture and/or other fluid collection within scope of the protocol and local law and regulations
  • With supervision, perform clinical assessments (vital signs, phlebotomy, ECG, etc) within scope of the protocol, local law and regulations
  • Process, package and ship laboratory specimens as required per protocol and IATA regulations, if applicable
  • Track, order and maintain inventory of all laboratory and study related supplies throughout course of the clinical trial
  • Enter source data into the sponsor's and/or vendor’s data portal and resolve basic queries in a timely manner under the direction of the Clinical Research Coordinator
  • Communicate with coworkers, leadership, study subjects, sponsors, CROs, and vendors under the direction of the Clinical Research Team
  • Understand good documentation practices when collecting, transferring data to sponsor/CRO data capture systems and resolving queries under the direction of the Clinical Research Coordinator
  • Understand the informed consent process with emphasis on ensuring initial and ongoing consent of study subjects
  • Understand basic elements of regulatory documentation required to initiate, maintain and close a clinical research trial
  • Understand and participate in patient recruiting tasks including but not limited to prescreening potential subjects for clinical research trials either via phone or in person
  • Maintain confidentiality of patient protected health information, sponsor confidential information and Velocity confidential information
  • Ability to escalate potential patient safety issues such as adverse events, serious adverse events, and adverse events of special interest to the Clinical Research Team
  • Cleaning, organizing, and disinfecting the patient care, lab and lab equipment areas as needed
  • Prepare source document charts, copy and/or file medical records and study related documents as required.
  • Perform front office duties as needed including but not limited to answering phones, scheduling subjects, making reminder calls and updating patient tracking systems.
  • Other duties as assigned

Education/Experience:

  • High School Graduate and/or technical degree with minimum of 1 year of relevant experience in life sciences industry

Required Licenses/Certifications:

  • Phlebotomy if applicable and required by state law
  • Intramuscular dose administration and preparation if applicable and required by state law

Required Skills:

  • Demonstrated knowledge of medical terminology
  • Demonstrated ability to use the following technology: Computers, Microsoft Office software, fax, copier, and multi-line telephone.
  • Understanding of verbal, written, and organizational skills
  • Demonstrated ability to work as a team player
  • Demonstrated ability to read, write, and speak English
  • Demonstrated ability to multi-task
  • Demonstrated ability to follow written guidelines
  • Demonstrated ability to be flexible/adapt as daily schedule may change rapidly

Required Physical Abilities:

  • Sit or stand for long periods of time
  • Communicate in person and by a telephone
  • Limited walking required
  • Limited to lifting up to 30 pounds

NOTE: The above Job Description is intended to communicate the general function of the mentioned position and by no means should be considered an exhaustive or complete outline of the specific tasks and functions that will be required.  Additionally, specific tasks and duties of the position are subject to change as the Company, the department and circumstances change.  All employees are expected to perform their duties within their ability as required by the job and/or as requested by management.



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