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Clinical Study Assistant Jobs in Virginia (NOW HIRING)

Program Assistant

Norfolk, VA · On-site

$36K - $46K/yr

... Clinical Trials Consortium (ACTC) studies. Primarily works out in the community with the target ... * Assist with the development and dissemination of outreach/informational materials and media ...

Showing results 41-60

Clinical Study Assistant information

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$11

$20

$28

How much do clinical study assistant jobs pay per hour?

As of Aug 16, 2026, the average hourly pay for clinical study assistant in Virginia is $20.06, according to ZipRecruiter salary data. Most workers in this role earn between $16.44 and $23.12 per hour, depending on experience, location, and employer.

What is a clinical study assistant?

Clinical Study Assistants are professionals who support the conduct of clinical trials by handling administrative tasks, maintaining study documentation, and ensuring regulatory compliance. They work closely with clinical research teams to coordinate schedules, communicate with study sites, and help manage trial materials. Their role is crucial in ensuring that clinical studies run smoothly, efficiently, and according to protocols and regulatory guidelines.

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

To thrive as a Clinical Study Assistant, you need strong organizational skills, attention to detail, and a background in life sciences or related fields, often supported by a bachelor's degree. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and regulatory documentation processes is typically required. Effective communication, teamwork, and problem-solving skills help you navigate complex study protocols and collaborate with diverse stakeholders. These abilities are crucial for ensuring the accuracy, compliance, and smooth operation of clinical research studies.

What are the main challenges a clinical study assistant might face when supporting clinical trial operations?

A Clinical Study Assistant often encounters challenges such as managing multiple tasks under tight deadlines, ensuring accurate documentation, and coordinating communication between research teams, sponsors, and regulatory bodies. Additionally, adapting to evolving study protocols and maintaining compliance with strict regulatory requirements can be demanding. Strong organizational skills, attention to detail, and proactive communication are essential for navigating these challenges successfully.

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

AspectClinical Study AssistantClinical Research Coordinator
CredentialsTypically requires a bachelor's degree in health sciences or related fieldUsually requires a bachelor's degree, often with additional certifications in clinical research
Work EnvironmentSupports clinical trials in hospitals, research centers, or pharmaceutical companiesManages entire clinical studies, coordinating between sites, staff, and sponsors
Employer & IndustryHospitals, research institutions, pharmaceutical companiesAcademic medical centers, hospitals, research organizations
Search & Comparison IntentOften compared for entry-level roles supporting clinical trialsCompared for roles with broader responsibilities in clinical study management

The Clinical Study Assistant primarily supports clinical trial activities by assisting with data collection and documentation, while the Clinical Research Coordinator manages the overall conduct of the study, including patient recruitment and compliance. Both roles require similar educational backgrounds but differ in scope and responsibilities within the clinical research process.

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 Assistant jobs?

Cities in Virginia with the most Clinical Study Assistant job openings:

Infographic showing various Clinical Study Assistant job openings in Virginia as of August 2026, with employment types broken down into 2% As Needed, 76% Full Time, 16% Part Time, and 6% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $41,718 per year, or $20.1 per hour.

Clinical Research Sub-Investigator (NP/PA)

ObjectiveHealth

Richmond, VA • On-site

Full-time

Re-posted 7 days ago


Job description

Description

Clinical Research Sub-Investigator (NP/PA) 

ObjectiveHealth is seeking a licensed Nurse Practitioner (NP) or Physician Assistant-Certified (PA-C) to serve as a Sub-Investigator at our Richmond, VA research site. This is a unique opportunity for an advanced practice provider in Internal Medicine, Family Medicine, or a related field to contribute to innovative clinical research.


ObjectiveHealth is a clinical research company transforming how research is conducted at the point of care. Using our proprietary technology, we aim to:

  • Increase patient access to research trials within our communities
  • Provide physicians with enhanced care options for current patients
  • Deliver superior clinical research enrollment metrics to Pharma sponsors

All with the ultimate goal of Improving Patient Outcomes at the Point of Care. We want you to join us in doing just that.


Key Responsibilities:

  • Serve as the Sub Investigator for assigned clinical trials, ensuring overall study oversight.
  • Oversee and enforce compliance with study protocols while prioritizing subject safety at all times.
  • Conduct and document physical examinations and medical assessments in accordance with research protocol requirements.
  • Provide continuous medical oversight throughout all phases of the clinical trial lifecycle.
  • Collaborate effectively with study coordinators, site staff, and other research team members to ensure smooth study execution.
  • Participate in sponsor meetings, site initiation visits, monitoring visits, and audits as needed.
  • Maintain strict compliance with GCP, ICH guidelines, FDA regulations, and internal SOPs.

Qualifications:

  • Licensed Nurse Practitioner (NP) or Physician Assistant-Certified (PA-C) with an active license in the state of Virginia.
  • Leadership experience in clinical or healthcare settings is preferred.
  • Ability to perform study-related clinical assessments and procedures under the guidance of the Principal Investigator.
  • Strong attention to detail and commitment to maintaining high ethical, clinical, and regulatory standards.
  • Excellent communication and interpersonal skills, with the ability to collaborate effectively in a multidisciplinary research environment.

Requirements

This job requires legal authorization to work in the US. We are not currently accepting work visas. ObjectiveHealth is an EEO Employer and an E-Verify participant