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Clinical Study Jobs in Virginia (NOW HIRING)

Liaise with the clinical study team to resolve outstanding issues identified during filing and/or quality reviews. * Provide extensive technical support for the study team when initiating the TMF.

$68K - $93K/yr

Submission of study related activities are completed and timely. Coordinates multiple clinical trials simultaneously or clinical trials with unique complexity. Maintains all required documentation ...

$68K - $93K/yr

Submission of study related activities are completed and timely. Coordinates multiple clinical trials simultaneously or clinical trials with unique complexity. Maintains all required documentation ...

Advanced level of competency connecting the study protocol, scientific principles and clinical trial requirements to the day-to-day clinical trial execution activities. Evaluate and ensure effective ...

Advanced level of competency connecting the study protocol, scientific principles and clinical trial requirements to the day-to-day clinical trial execution activities. Evaluate and ensure effective ...

Advanced level of competency connecting the study protocol, scientific principles and clinical trial requirements to the day-to-day clinical trial execution activities. Evaluate and ensure effective ...

Clinical Research Coordinator

Henrico, VA · On-site

$22.50 - $29.75/hr

Clinical Research Coordinator (CRC) About Tekton Research: Tekton Research is a growth-oriented ... Recruit, screen, consent, and schedule study participants according to protocol requirements.

Showing results 21-40

Clinical Study information

See Virginia salary details

$21.8K

$124.2K

$204.2K

How much do clinical study jobs pay per year?

As of Aug 7, 2026, the average yearly pay for clinical study in Virginia is $124,215.00, according to ZipRecruiter salary data. Most workers in this role earn between $84,300.00 and $155,700.00 per year, depending on experience, location, and employer.

What is a clinical study?

Clinical studies are research investigations conducted with human volunteers to evaluate the safety, effectiveness, and side effects of medical treatments, drugs, devices, or interventions. These studies follow strict scientific and ethical guidelines and are usually carried out in several phases before a treatment can be approved for widespread use. Clinical studies help determine whether new approaches to prevention, diagnosis, or therapy are safe and effective for people. Participation in clinical studies is voluntary and can contribute to advancements in medical science.

What are some common challenges faced when managing multiple clinical studies simultaneously?

Professionals involved in clinical studies often juggle several projects at once, which can present challenges such as balancing competing timelines, ensuring regulatory compliance across studies, and coordinating with diverse teams. Effective project management, clear communication, and strong organizational skills are key to addressing these challenges. Utilizing project management tools and maintaining detailed documentation can help keep studies on track and reduce the risk of errors or delays.

Do clinical studies pay well?

Clinical study roles, such as clinical research coordinators or assistants, typically offer moderate pay that varies by experience, location, and employer. Entry-level positions may start at lower wages, while experienced professionals or those with specialized skills can earn higher salaries, especially when working on complex or long-term studies.

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

AspectClinical StudyClinical Research Coordinator
CredentialsOften requires a degree in health sciences, nursing, or related fields; certifications like CCRP are commonTypically holds a bachelor's degree in health sciences, nursing, or related fields; certifications like CCRP or CRC are advantageous
Work EnvironmentConducted in hospitals, clinics, or research facilities; involves direct patient interaction and data collectionWorks in research sites, hospitals, or clinics; manages study logistics and coordinates between teams
Employer & IndustryPharmaceutical companies, academic institutions, CROsResearch institutions, hospitals, pharmaceutical companies

While both roles are integral to clinical research, a Clinical Study typically refers to the overall research process or specific studies, whereas a Clinical Research Coordinator is a professional who manages and oversees the day-to-day operations of clinical trials. Understanding these distinctions helps in choosing the right career path or job search focus.

What jobs are there in clinical studies?

Jobs in clinical studies include clinical research coordinators, clinical research associates, data managers, regulatory affairs specialists, and study nurses. These roles involve tasks such as patient recruitment, data collection, monitoring trial progress, and ensuring compliance with regulations, often requiring knowledge of Good Clinical Practice (GCP) and relevant certifications. The work environment is typically a research facility, hospital, or pharmaceutical company, with schedules varying from full-time to part-time depending on the role.

What are the key skills and qualifications needed to thrive as a clinical study coordinator?

To thrive as a Clinical Study Coordinator, you need a solid understanding of clinical research protocols, regulatory guidelines like GCP, and often a degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and sometimes certification such as CCRC or CCRA is typically required. Strong organizational skills, attention to detail, and effective communication are crucial soft skills for coordinating multiple tasks and interacting with diverse stakeholders. These skills ensure compliance, accurate data collection, and smooth trial operations, which are vital for the integrity and success of clinical studies.
What are the most commonly searched types of Clinical Study jobs in Virginia? The most popular types of Clinical Study jobs in Virginia are:
What cities in Virginia are hiring for Clinical Study jobs? Cities in Virginia with the most Clinical Study job openings:
Infographic showing various Clinical Study job openings in Virginia as of August 2026, with employment types broken down into 2% As Needed, 69% Full Time, 21% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $124,215 per year, or $59.7 per hour.

Ophthalmology Technician / Study Coordinator BILINGUAL

EMERSON CLINICAL RESEARCH INSTITUTE

Falls Church, VA

$43K - $50K/yr

Full-time

Medical, Dental, Retirement

Re-posted 6 days ago


Job description

Emerson Clinical Research Institute (ECRI) is a network of research sites focused on working with community based clinics in the D.C, VA, and MD area. We conduct phase II-IV clinical research studies in community clinics. These clinics are focused on providing health care services to the minority populations, that don't otherwise have access to research opportunities. Our studies are industry sponsored research protocols in for adults and pediatric patients (study participants).
We are looking for an Ophthalmology Technician that is ready to take the next step up in their carrier. Here you won’t be doing standard work. This position will allow the candidate to be fully engaged in the development of new medical treatments. The candidate will work doing BCVA, OCT, FA and a variety of other procedures, in order to support work in the conduct of clinical research.

The second part of this position the candidate will learn to manage a clinical research protocol, recruit and educate patients on the importance of participating in clinical research studies.

The position is intended to support research studies conducted at our two Falls Church VA locations.

TIME COMMITTMENT:


• This is a salary position with a minimum 40 hrs a week, The position will start at 20hrs a week for the first 2 months until the candidate is fully trained in the job skills.

• May also include some weekends if required.
RESPONSIBILITES INCLUCDE BUT ARE NOT LIMITED TO:

The position is responsible and accountable for recruitment directives, meeting financial goals, and the overall study operations. The study coordinator also significantly participates in the clinical trial coordination process.

· Promoting the mission of ECRI to function as an Integrated Site Network providing unparalleled service to our clinical trial partners

· Meeting and exceeding priorities as discussed quarterly with direct supervisor

· Managing daily site operations.

· Ensuring adherence to ECRI’s Standard Operating

· Ensuring the site’s compliance with all federal, local, and regulatory requirements and company procedures.

· Work with study participants on completion of study related visits, as well as follow-up and reminder phone calls.

· Subject recruitment.

· Work closely with pharma sponsor clinical research professionals in the processing and preparations for submitting regulatory documents.

· Data entry of case report forms, and study visits across all study platforms within a maximum of 24hrs from the time data as collected.

· Development of case report forms.

· Other clinical research activities as assigned.

· Support other ECRI research studies.

· Management of all study records for protocols assinged.


MINIMUM REQUIREMENTS:

· Bilingual English and Spanish

· 2 degree or equivalent in health-related field of study.

· Ability to successfully adapt to a constantly changing environment;

· Minimum of 3 years of experience as an Ophthalmology Technician

o Auto-refraction

o Refraction

o Trial-lens refraction

o OCT and FA photography

· Must be able to utilize computer applications such as Microsoft Office or other web-based systems;

· Must have superior interpersonal and communication skills with a strong customer service focus.

· Be friendly and engaging and demonstrate excellent organizational and time management skills.

· Be able to conduct independent research activities.

· Be extremely motivated and self-starter.

· Be able to meet deadlines.

· Participate in occasional health fair events, and community outreach activities.

WORKING CONDITIONS:

This position does involve direct contact with patients and includes performing phlebotomy procedures, as needed. Occupational Health and Safety Risks include potential exposure to blood borne and airborne pathogens, thus candidate must ensure to always use universal precautions when handling biological samples, and supplies. This position may involve occasional travel, including airplane travel, to attend ECRI Leadership Meetings and Investigator’s Meetings.

Company Description

Emerson Clinical Research Institute (ECRI) is a network of research sites focused on working with community based clinics in the D.C, VA, and MD area. We conduct phase II-IV clinical research studies in community clinics. These clinics are focused on providing health care services to the minority populations, that don't otherwise have access to research opportunities. Our studies are industry sponsored research protocols in for adults and pediatric patients (study participants).

The position is intended to support research studies conducted at the various ECRI D.C locations.