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Socra Jobs in Virginia (NOW HIRING)

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

Richmond, 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 ...

Sentara Health Plans

Research Nurse

Norfolk, VA · On-site

$70 - $90/hr

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 ...

Socket.dev

Clinical Research Coordinator (DCR)

Norfolk, VA · On-site

$50 - $76/hr

Certified Clinical Research Coordinator (SOCRA or ACRP) - preferred DaVita Clinical Research (DCR), a wholly owned subsidiary of DaVita Inc., is the research arm of DaVita.DCR innovates through ...

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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 Sep 5, 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 Coordinator (CRC)

Azimuth Research Group

Portsmouth, VA • On-site

$60 - $80/hr

Other

Posted 4 days ago

Key responsibilities

  • Coordinate operational aspects of clinical research projects across assigned study sites, including military treatment facilities.

  • Support the development, maintenance, and review of regulatory documents such as ICFs, protocol amendments, and IRB submissions.

  • Assist in participant screening, eligibility verification, recruitment tracking, and scheduling in alignment with protocol requirements.

Job description

Company Overview

Azimuth Research Group (Azimuth) is a global research organization that leverages point of care data to address challenging questions for clients in the pharmaceutical and biotechnology industry, as well as academia. Our vision is to remake the biopharmaceutical and overall research industry by embedding continuous, adaptive research into healthcare delivery ecosystems. We accelerate the discovery and development of therapies with intelligent precision–ultimately improving patient outcomes globally.

Work Location

Hampton Roads Area (Portsmouth, VA)

Job Title

Clinical Research Coordinator (CRC)

Job Status

Full-time Employment

Job Summary

The CRC is responsible for day-to-day clinical trial coordination activities including site communication, participant screening support, data collection oversight, regulatory documentation, and protocol compliance. This role requires working knowledge of the DoD Military Health System, including familiarity with MHS GENESIS (Cerner), military medical operations, clinical workflows within military treatment facilities (MTFs), and DoD clinical research governance. The CRC ensures operational excellence in studies involving active-duty service members, veterans, and beneficiaries while maintaining the highest standards of data integrity and participant safety.

Clinical Operations

Reports to: Clinical Operations Study Manager

Education

Bachelor’s degree, preferably with a focus in science, public health, healthcare administration, or related field required.

Licensure

N/A

Clinical Experience

N/A

Research Experience

At least 5 years of clinical research experience required, preferably within the DoD, VA, or other US government clinical research settings.

Research Certification

SOCRA/ACRP certification preferred

DOD Site Requirements
  • Ability to obtain and maintain a security clearance per US government requirements.
  • Up to date immunizations.
Core Skills & Experience
  • Strong understanding of clinical research operations, GCP, and human subjects research principles.
  • Ability to perform study procedures with high accuracy and attention to protocol detail.
  • Ability to support multiple studies, priorities and deadlines in a fast-paced research environment.
  • Strong communication skills, professionalism, and ability to collaborate with interdisciplinary teams.
  • Proficiency with Microsoft Office, EDC systems, and remote collaboration tools.
  • Experience within DoD, VA, or other US government healthcare environments is highly desirable.
  • Working knowledge of the Department of Defense Military Health System, including clinical workflows and research oversight processes.
  • Experience with EHR systems such as MHS GENESIS (Cerner) preferred.
Job Responsibilities
  • Coordinate operational aspects of clinical research projects across assigned study sites, including military treatment facilities.
  • Support the development, maintenance, and review of regulatory documents (e.g., ICFs, protocol amendments, IRB submissions).
  • Assist in participant screening, eligibility verification, recruitment tracking, and scheduling in alignment with protocol requirements.
  • Serve as a point of contact for site personnel, investigators, and DoD clinical research offices.
  • Ensure all study activities meet GCP, FDA, ICH, and DoD Human Research Protection Program (HRPP) requirements.
  • Support data abstraction from MHS systems and ensure accurate, timely entry into EDC and study databases.
  • Monitor protocol adherence and elevate deviations or safety concerns appropriately.
  • Prepare for site visits, audits, and monitoring activities; support follow-up and documentation.
  • Collaborate with cross-functional stakeholders, including biostatistics, data science, and clinical operations teams.
  • Maintain complete study records, logs, and documentation in compliance with Azimuth SOPs and DoD regulatory frameworks.
  • Schedule flexibility to support calls related to patients that may occur early in the morning or late in the evening as well as potentially on the weekends.
  • Contribute to process improvement and quality initiatives across Azimuth’s research operations.
  • Ability to perform protocol procedures as needed (e.g. phlebotomy, ECGs, biological specimen collection).
  • Attend study and staff meetings as required.
  • Assist with regulatory submissions as needed.
Extent of Travel

Up to 25%, including travel to military treatment facilities and partner sites.

Management or Individual Contributor

Individual Contributor

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