ZipRecruiter

Log In

1

Socra Jobs in Virginia (NOW HIRING)

Sentara Healthcare

Research Nurse

Norfolk, VA · On-site

Specialty certification Certified Clinical Research Professional (SOCRA CCRP or ACRP-CP) or Certified Clinical Research Coordinator (CCRC) is required within 3 years of employment. Experience: * 2 ...

Sentara

Research Nurse

Norfolk, VA

$10K/mo

Specialty certification Certified Clinical Research Professional (SOCRA CCRP or ACRP-CP) or Certified Clinical Research Coordinator (CCRC) is required within 3 years of employment. Experience: * 2 ...

Sentara

Research Nurse

Norfolk, VA · On-site

Specialty certification Certified Clinical Research Professional (SOCRA CCRP or ACRP-CP) or Certified Clinical Research Coordinator (CCRC) is required within 3 years of employment. Experience: * 2 ...

Tekton Research Inc

Clinical Research Coordinator

Henrico, VA · On-site

$22.50 - $29.75/hr

Current ACRP-CRC or SOCRA certification. * Advanced degree in Nursing, Public Health, Clinical Research, or a related healthcare field. * Experience working on industry-sponsored or multi-center ...

next page

Showing results 1-20

All JobsSocra JobsSocra Jobs in Virginia

Socra information

See Virginia salary details

$11

$40

$69

How much do socra jobs pay per hour?

As of Aug 26, 2026, the average hourly pay for socra in Virginia is $40.77, according to ZipRecruiter salary data. Most workers in this role earn between $28.61 and $52.21 per hour, depending on experience, location, and employer.

What is a Socra?

A Socra job typically refers to a role in clinical research, often associated with the certification provided by the Society of Clinical Research Associates (SoCRA). Professionals in this field are responsible for ensuring clinical trials comply with regulatory requirements, ethical guidelines, and study protocols. They may work as Clinical Research Associates (CRAs), Clinical Research Coordinators (CRCs), or other related positions. Their duties include monitoring clinical trials, maintaining accurate documentation, and safeguarding patient safety throughout the study process. Obtaining SoCRA certification can enhance credibility and career opportunities in the clinical research industry.

What are SOC RAs (Security Operations Center Research Analysts)?

SOC RAs, or Security Operations Center Research Analysts, are professionals who monitor, detect, investigate, and respond to cybersecurity threats within an organization. They analyze security alerts, assess vulnerabilities, and work closely with other IT and security staff to ensure incidents are managed effectively. Their role is critical in maintaining the organization’s security posture and protecting sensitive data from potential breaches. SOC RAs typically use various security tools and techniques to identify and mitigate risks in real-time.

What are the key skills and qualifications needed to thrive as a Clinical Research Associate (SOCRA), and why are they important?

To thrive as a Clinical Research Associate (SOCRA), you need a solid understanding of clinical trial processes, regulatory guidelines, and a relevant life sciences degree or certification such as SOCRA's CCRP. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and Good Clinical Practice (GCP) guidelines is typically required. Strong attention to detail, organizational skills, and effective communication are crucial soft skills for managing study protocols and collaborating with research teams. These competencies ensure the integrity of clinical trials, regulatory compliance, and the successful advancement of medical research.

What are some common challenges faced by Socra (Study Coordinator) professionals when managing multiple clinical trials simultaneously?

Socra professionals, or Study Coordinators, often manage several clinical trials at once, which can present challenges in prioritizing tasks, maintaining regulatory compliance, and ensuring accurate documentation across studies. Balancing communication with different research teams, investigators, and sponsors while meeting tight deadlines requires strong organizational and multitasking skills. Staying updated with protocol amendments and managing participant recruitment and retention can also be demanding aspects of the role.

What is the difference between Socra vs Data Analyst?

AspectSocraData Analyst
Required CredentialsTypically requires a degree in social sciences, research methods, or related fields; certifications in data collection or analysis are a plusRequires a degree in statistics, mathematics, or related fields; certifications like CAP or Microsoft Data Analyst are common
Work EnvironmentPrimarily fieldwork, interviews, and data collection in social or community settingsOffice-based, analyzing data sets, creating reports, and visualizations
Employer & Industry UsageUsed by research organizations, NGOs, and government agencies for social researchUsed across industries like finance, marketing, healthcare, and technology for data-driven decision making

While both Socra and Data Analyst roles involve data handling, Socra focuses more on social research and fieldwork, whereas Data Analysts primarily analyze digital data in office settings. The roles share similar educational backgrounds and certifications but differ in work environment and industry application.

What are popular job titles related to Socra jobs in Virginia?

For Socra jobs in Virginia, the most frequently searched job titles are:

What job categories do people searching Socra jobs in Virginia look for?

The top searched job categories for Socra jobs in Virginia are:

Socra jobs near you
Infographic showing various Socra job openings in Virginia as of August 2026, with employment types broken down into 56% Full Time, and 44% Part Time. Highlights an 100% In-person job distribution, with an average salary of $84,808 per year, or $40.8 per hour.

Clinical Research Assistant

Prism Vision Group

Fairfax, VA • On-site

$46K - $96K/yr

Full-time

Posted 12 days ago

PRISM Vision Group rating

7.2

Company rating: 7.2 out of 10

Based on 15 frontline employees who took The Breakroom Quiz

Job description

This exempt, onsite role is located at Retina Group of Washington, Fairfax, VA location, which is part of Prism Vision Group.

Compensation Range: $46,675.20 - $96,969.60/annual (Dependent on Experience)

The Clinical Research Assistant reports to the RGW Office Manager and RGW Research Lead and will aid in the coordination and conduct of research under the supervision of a designated physician. The Clinical Research Assistant will perform a variety of duties involved in the collection, compilation, documentation and analysis of clinical research data. The Clinical Research Assistant will develop knowledge of the research studies, rationale, subjects and procedures associated with the studies as designated by the Senior/Lead Clinical Research Coordinator. This  position is designed specifically to develop into a Clinical Research Coordinator and travels between multiple locations as needed.

Role and Responsibilities:

  • Assists in recruitment efforts to screen potential patients for eligibility for studies.
  • Obtains informed consent from patients and conducts study visits for clinical trials
  • Creates Case Report Forms
  • Completes assessments on study subjects as per protocol
  • Documents study assessments
  • Enters study data into EDC systems
  • Collects, processes, stores and shipslab specimens; documents lab procedures, lab results and follows up with patients and medical staff as necessary
  • Coordinates, monitors visits with CRAs for each trial to ensure accurate documentation; makes corrections to data as necessary
  • Assists during Sponsor and FDA audits
  • Responsible for submissions and reports to the IRB; maintains documentation of IRB communications and decisions
  • Documents adverse events and notifies PI, sponsor and IRB under CRC guidance
  • Assumes test article accountability
  • Possesses a sound and in-depth understanding of each protocol that has been assigned as a primary responsibility
  • Maintains compliance with Good Clinical Practice; Clinical Safety Data Management, 21 CFR, and has IATA certification
  • Travels to investigator meetings
  • Participates in weekly meetings with the research team, provides study metrics
  • Responds to requests in a timely manner, gives/receives correct information, encourages dialogue and follow-through, secures accurate signatures, maintains files in an organized and up-to-date manner

Qualifications:

Education: Associates or Bachelors Degree preferred in Science or related field. Equivalent relevant experience and/or training in lieu of education is acceptable.

Experience: 1+ years’ relevant experience (e.g. research, clinical, interaction with study population, program coordination)

Knowledge/Skills/Experience:

• Excellent Excel, Word, PowerPoint and reporting skills

• Excellent interpersonal skills to deal effectively with patients, physicians, clinicians and administrators

• Excellent organizational skills and self-management skills to independently manage workflow

• Ability to prioritize

• Meticulous attention to detail

• Knowledge of medical terminology

• Knowledge of good clinical practice, FDA, OHRP, HIPAA policies

• Experience using Microsoft Office Suite

• Certification through either ACRP or SoCRA highly preferred

Qualifications:

Qualifications:

Education: Associates or Bachelors Degree preferred in Science or related field. Equivalent relevant experience and/or training in lieu of education is acceptable.

Experience: 1+ years’ relevant experience (e.g. research, clinical, interaction with study population, program coordination)

Knowledge/Skills/Experience:

• Excellent Excel, Word, PowerPoint and reporting skills

• Excellent interpersonal skills to deal effectively with patients, physicians, clinicians and administrators

• Excellent organizational skills and self-management skills to independently manage workflow

• Ability to prioritize

• Meticulous attention to detail

• Knowledge of medical terminology

• Knowledge of good clinical practice, FDA, OHRP, HIPAA policies

• Experience using Microsoft Office Suite

• Certification through either ACRP or SoCRA highly preferred

Education:UNAVAILABLEEmployment Type: FULL_TIME

What PRISM Vision Group employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom

Apply