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Remote Virtual Research Assistant Jobs in Washington

MAPMG researchers and staff support innovative ideas, ensuring quality care, educational ... To provide virtual urgent care * To keep current with telemedicine guidance, attends meetings and ...

... remote opportunity ideal for veterinarians looking to pick up additional work, explore virtual care ... These tools assist our recruitment team but do not replace human judgment. Final hiring decisions ...

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Remote Virtual Research Assistant information

What is the difference between Remote Virtual Research Assistant vs Virtual Data Entry Specialist?

AspectRemote Virtual Research AssistantVirtual Data Entry Specialist
Required CredentialsBasic research skills, sometimes a degree in related fieldsTyping speed, accuracy, basic computer skills
Work EnvironmentRemote, flexible hours, project-basedRemote, task-focused, often repetitive
Employer & Industry UsageResearch firms, academic support, market researchData management companies, administrative support
Common Search & Comparison IntentUnderstanding research tasks, skills neededData entry tasks, accuracy requirements

The Remote Virtual Research Assistant typically handles research, analysis, and information gathering tasks, requiring some research skills and critical thinking. In contrast, a Virtual Data Entry Specialist focuses on inputting data accurately and efficiently, often with minimal research involved. Both roles are remote and flexible but serve different functions within organizations.

What are popular job titles related to Remote Virtual Research Assistant jobs in Washington?

For Remote Virtual Research Assistant jobs in Washington, the most frequently searched job titles are:

What cities in Washington are hiring for Remote Virtual Research Assistant jobs?

Cities in Washington with the most Remote Virtual Research Assistant job openings:

Clinical Research Assistant

Allen Spolden

Silver Spring, MD • Remote

$45K - $55K/hr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 24 days ago


Job description

This is a remote position.

Position Overview

We are seeking a motivated and detail-oriented Clinical Research Assistant to join our growing clinical operations team. In this role, you will support the coordination and administration of clinical research studies while ensuring study documentation, data quality, and regulatory compliance are maintained throughout the research process.

This position is ideal for someone with excellent organizational skills, strong attention to detail, and an interest in contributing to clinical research in a remote environment.

Essential Responsibilities
  • Assist with the day-to-day management of assigned clinical studies.
  • Maintain investigator site files, regulatory binders, and essential study documents.
  • Prepare, review, and file research documentation in accordance with study requirements.
  • Support participant scheduling and study visit coordination.
  • Enter, verify, and reconcile clinical data within electronic research systems.
  • Monitor study timelines and assist with tracking project deliverables.
  • Communicate effectively with investigators, sponsors, study participants, and internal research teams.
  • Identify and escalate documentation discrepancies or protocol deviations when appropriate.
  • Ensure research activities are conducted in compliance with ICH Good Clinical Practice (GCP), study protocols, and applicable regulatory requirements.
  • Perform additional administrative and research support duties as assigned.


RequirementsQualifications
Required
  • Bachelor's degree in Life Sciences, Health Sciences, Nursing, Public Health, or a related discipline, or equivalent healthcare experience.
  • Strong organizational and problem-solving abilities.
  • Excellent verbal and written communication skills.
  • High level of accuracy and attention to detail.
  • Proficiency with Microsoft Office and web-based software applications.
  • Ability to manage multiple priorities while working independently in a remote setting.
Preferred
  • Previous experience supporting clinical research or healthcare operations.
  • Familiarity with ICH-GCP guidelines and FDA regulations.
  • Experience using Electronic Data Capture (EDC), CTMS, or eTMF systems.
  • Knowledge of clinical trial documentation and research workflows.
Work Schedule
  • Full-time
  • Monday through Friday
  • Standard business hours


BenefitsBenefits
  • Competitive salary
  • Comprehensive medical, dental, and vision coverage
  • 401(k) with employer contribution
  • Paid time off and company holidays
  • Remote work environment
  • Professional development and career advancement opportunities