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Clinical Study Associate Jobs in Virginia (NOW HIRING)

Associate Veterinarian

Lynchburg, VA · On-site

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Introduction Join us as an Associate Veterinarian at VCA Boonsboro Animal Hospital, and you'll ... Opportunities to participate in a robust Clinical Studies program Discover Additional Benefits ...

Associate Veterinarian

Richmond, VA · On-site

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Join us as an Associate Veterinarian at VCA Pets First Animal Hospital , and you'll quickly ... Opportunities to participate in a robust Clinical Studies program Discover Additional Benefits ...

Postdoctoral Associate Apply now Back to search results Job no: 536804 Work type: Research Faculty ... From basic functional circuit dissection in animals to human clinical studies, we ask how network ...

Showing results 41-60

Clinical Study Associate information

See Virginia salary details

$12

$31

$54

How much do clinical study associate jobs pay per hour?

As of Aug 15, 2026, the average hourly pay for clinical study associate in Virginia is $31.27, according to ZipRecruiter salary data. Most workers in this role earn between $20.96 and $41.25 per hour, depending on experience, location, and employer.

What is a clinical study associate?

Clinical Study Associates (CSAs) are professionals who support the planning, execution, and monitoring of clinical trials in the pharmaceutical, biotechnology, or medical device industries. They help coordinate study logistics, maintain study documentation, and ensure compliance with regulatory requirements. CSAs often work closely with Clinical Research Associates, study coordinators, and investigators to ensure that trials are conducted according to protocol and timelines. Their role is essential in ensuring the accuracy and integrity of data collected during clinical research.

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

AspectClinical Study AssociateClinical Research Coordinator
CredentialsBachelor's degree, often in life sciences; certifications like CCRP or CCRA beneficialBachelor's degree in health sciences or related field; certifications like CCRP advantageous
Work EnvironmentPharmaceutical companies, CROs, clinical trial sitesHospitals, clinics, research centers
Job FocusMonitoring clinical trials, ensuring protocol compliance, data accuracyManaging daily trial activities, patient recruitment, data collection
Employer & Industry UsageCommonly employed in pharma and CROsPrimarily in healthcare and academic research settings

Both roles involve clinical trial oversight but differ in focus: Clinical Study Associates primarily monitor and ensure compliance during trials, while Clinical Research Coordinators manage daily trial operations and patient interactions. Understanding these distinctions helps in choosing the right career path or job search focus.

What are the key skills and qualifications needed to thrive as a clinical study associate, and why are they important?

To thrive as a Clinical Study Associate, you need a strong understanding of clinical research processes, regulatory requirements, and typically a life sciences degree. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and GCP certification are commonly required. Attention to detail, organizational skills, and effective communication set top performers apart in this role. These competencies ensure accurate study documentation, regulatory compliance, and smooth coordination across research teams.

What are some common challenges clinical study associates face when managing multiple clinical trials simultaneously?

Clinical Study Associates often juggle several clinical trials at once, which can present challenges such as prioritizing competing deadlines, maintaining accurate documentation for each study, and ensuring consistent communication with cross-functional teams. Staying organized and proactive is essential, as unforeseen protocol amendments or site issues can arise. Building strong relationships with site staff and utilizing effective project management tools can help CSAs navigate these complexities and deliver high-quality results.

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 Associate jobs?

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

Infographic showing various Clinical Study Associate 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 $65,041 per year, or $31.3 per hour.

$67K - $103K/yr

Full-time

Posted 7 days ago


US Oncology rating

7.1

Company rating: 7.1 out of 10

Based on 109 frontline employees who took The Breakroom Quiz

380th of 887 rated healthcare providers


Job description

Overview

This is an entry-level exempt management position-Supervises the clinical research staff members in accordance with USON SOP and ICH GCP guidelines. Responsible for ensuring at the administrative level that all research activities are coordinated with affected departments within the practice. Coaches and develops staff. Collaborates in the development of research accountability standards and identifies areas for improvement. Ensures site research quality by practicing in compliance with US Oncology Research, Inc. (USOR) Standard Operating Procedures (SOP), principles of Good Clinical Practice (GCP) and applicable federal, state, and local regulations. Supports and adheres to the US Oncology Compliance Program, to include Code of Ethics and Business Standards.


Responsibilities
  • Supervises clinical research staff members in accordance with USOR SOP and ICH GCP guidelines. Responsible for ensuring at the administrative level that all research activities are coordinated with affected departments within the practice.

  • Coaches and develops staff. Participates in the recruitment, interviewing, hiring, assessing performance, recommending salary changes, and progressive discipline. Enforces adherence to company policies.

  • Collaborates in the development of research accountability standards, metrics, and reports and identifies areas for improvement. Collaborates with site research leader (SRL), upper management, and staff in the implementation of action plans designed to improve practice research operations and quality assurance functions.

  • Collaborates with the SRL, physicians of the practice, and other research management in the process of study selection for the research program.

  • Collaborates with SRL and upper management on the development of research budgets, financial objectives, and accrual targets.

  • May promote or market research program to the practice, community, and referring physicians.

  • May coordinate research activities with other (non-USOR) bases or sponsors.


Qualifications
  • Associates degree in a clinical or scientific related discipline or 8 years of experience equivalent.

  • Graduate of an accredited nursing program preferred

Business Experience -

  • Minimum 5 years clinical nursing experience or scientific related discipline required, preferably in oncology

  • Supervisory experience preferred, experience in clinical research preferred

  • If required in state of practice, current licensure as a registered (RN)

  • Current BCLS or ACLS certification for nurses

  • SoCRA or ARCP certification preferred

Specialized Knowledge/Skills -

  • Excellent communication skills

  • Strong ability to multitask, strong interpersonal skills

  • Must be able to work in a fast-paced, constantly changing environment

  • Knowledge and proficiency in all basic computer programs, Windows, Excel, etc.

  • Special knowledge of GCP and ICH guidelines preferred

  • Knowledge of medical terminology, nursing assessment, clinical medicine, diagnostic tests, radiology, pathology, pharmacology, hematology, oncology as it relates to clinical trials

Working Conditions:

Environment (Office, warehouse, etc.) –

  • Traditional office environment.

The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Exposure to communicable diseases, toxic substances, ionizing radiation, medical preparations and other conditions common to an

oncology/hematology clinic environment.

Physical Requirements (Lifting, standing, etc.) –

  • Large percent of time performing computer based work is required.

The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Requires full range of body motion including handling and lifting patients, manual and finger dexterity, and eye-hand coordination. Requires standing and walking for extensive periods of time. Occasionally lifts and carries items weighing up to 40 lbs. Requires corrected vision and hearing to normal range.

(This description is general in nature and is not intended to be an exhaustive list of all responsibilities. Other duties may be assigned as needed to meet company goals.)

 Pay Scale: The general pay scale for this position at BRCC is $67,458.15- $103,781.77. The actual hiring rate is dependent on many factors, including but not limited to prior work experience, education, job/position responsibilities, location, work performance, etc. 

Qualifications:
  • Associates degree in a clinical or scientific related discipline or 8 years of experience equivalent.

  • Graduate of an accredited nursing program preferred

Business Experience -

  • Minimum 5 years clinical nursing experience or scientific related discipline required, preferably in oncology

  • Supervisory experience preferred, experience in clinical research preferred

  • If required in state of practice, current licensure as a registered (RN)

  • Current BCLS or ACLS certification for nurses

  • SoCRA or ARCP certification preferred

Specialized Knowledge/Skills -

  • Excellent communication skills

  • Strong ability to multitask, strong interpersonal skills

  • Must be able to work in a fast-paced, constantly changing environment

  • Knowledge and proficiency in all basic computer programs, Windows, Excel, etc.

  • Special knowledge of GCP and ICH guidelines preferred

  • Knowledge of medical terminology, nursing assessment, clinical medicine, diagnostic tests, radiology, pathology, pharmacology, hematology, oncology as it relates to clinical trials

Working Conditions:

Environment (Office, warehouse, etc.) –

  • Traditional office environment.

The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Exposure to communicable diseases, toxic substances, ionizing radiation, medical preparations and other conditions common to an

oncology/hematology clinic environment.

Physical Requirements (Lifting, standing, etc.) –

  • Large percent of time performing computer based work is required.

The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Requires full range of body motion including handling and lifting patients, manual and finger dexterity, and eye-hand coordination. Requires standing and walking for extensive periods of time. Occasionally lifts and carries items weighing up to 40 lbs. Requires corrected vision and hearing to normal range.

(This description is general in nature and is not intended to be an exhaustive list of all responsibilities. Other duties may be assigned as needed to meet company goals.)

 Pay Scale: The general pay scale for this position at BRCC is $67,458.15- $103,781.77. The actual hiring rate is dependent on many factors, including but not limited to prior work experience, education, job/position responsibilities, location, work performance, etc. 

Education:UNAVAILABLEEmployment Type: FULL_TIME

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