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Weekend Research Jobs in Virginia (NOW HIRING)

King and Spalding LLP

Research Specialist

Mclean, VA · On-site

$86K - $108K/yr

Will be expected to serve on-call on a rotating basis, to support research requests after normal business hours and on weekends and holidays. QUALIFICATIONS: * Bachelor's degree required; a ...

Virginia Tech

Research Technician

Blacksburg, VA

$15.75 - $21.75/hr

Research Technician Apply now Back to search results Job no: 536801 Work type: Staff Senior ... on weekends Required Qualifications - Must be an effective communicator with excellent ...

Bloomberg Industry Group

Research Specialist

Arlington, VA · On-site

$66K - $82K/yr

Flexibility to work assigned business hours, including weekends and holidays as needed. Preferred Experience/Training: * Experience in an analyst, research, or client-facing support role within the ...

Alcanza Clinical Research

$23.50 - $31.25/hr

The Clinical Research Coordinator under the direction of the Site Manager/Director and the Principal/Sub Investigators conducts the following according to the study protocol, company processes ...

Bloomberg Industry Group

Research Specialist

Arlington, VA · On-site

$66K - $82K/yr

Flexibility to work assigned business hours, including weekends and holidays as needed. Preferred Experience/Training: * Experience in an analyst, research, or client-facing support role within the ...

Bloomberg Industry Group

Research Specialist

Arlington, VA · On-site

$66K - $82K/yr

Flexibility to work assigned business hours, including weekends and holidays as needed. Preferred Experience/Training: * Experience in an analyst, research, or client-facing support role within the ...

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Weekend Research information

What is a Weekend Research?

A Weekend Research job typically involves conducting research tasks during weekends, which can include data collection, literature reviews, experiments, or analysis depending on the field. These roles are often part-time and may be suited for students, professionals seeking extra income, or those unable to work during regular weekday hours. Weekend research positions can be found in academic institutions, private companies, or independent projects. Responsibilities and requirements vary by employer, but attention to detail, strong organizational skills, and the ability to work independently are usually important.

What are some common challenges faced by Weekend Research professionals, and how can they effectively manage their workload?

Weekend Research professionals often face the challenge of balancing tight deadlines and limited access to colleagues or resources during non-standard hours. To manage these challenges, it’s important to plan tasks ahead, utilize digital collaboration tools, and communicate clearly with team members about progress and needs before the weekend. Additionally, setting clear objectives and prioritizing tasks can help ensure efficient use of time, allowing for thorough and high-quality research even when support is limited.

What are the key skills and qualifications needed to thrive as a Weekend Researcher, and why are they important?

To thrive as a Weekend Researcher, you typically need strong analytical skills, attention to detail, and a relevant academic background or experience in research methods. Familiarity with data analysis tools, online research databases, and citation management systems is often required. Excellent time management, self-motivation, and clear written communication make someone stand out in this position. These skills and qualities are essential for producing accurate, timely, and well-organized research findings, especially within tight weekend deadlines.

What are the most commonly searched types of Research jobs in Virginia?

The most popular types of Research jobs in Virginia are:

What cities in Virginia are hiring for Weekend Research jobs?

Cities in Virginia with the most Weekend Research job openings:

Weekend Research jobs near you
Infographic showing various Weekend Research job openings in Virginia as of August 2026, with employment types broken down into 1% As Needed, 86% Full Time, 11% Part Time, and 2% Contract. Highlights an 81% Physical, 3% Hybrid, and 16% Remote job distribution.

Clinical Research Coordinator (CRC)

Azimuth Research Group

Portsmouth, VA • On-site

$60 - $80/hr

Other

Posted 3 days ago

New

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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