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Remote Clinical Research Assistant Volunteer Jobs

Essentia Health

Clinical Research Assistant

Duluth, MN · On-site +1

$18.69 - $27.85/hr

... assist investigators, clinical research nurses and others in the conduct of assigned clinical ... None FTE: 1 Possible Remote/Hybrid Option: Shift Rotation: Day Rotation (United States of America ...

WEP Clinical

Senior Clinical Research Associate

They conduct on-site and remote monitoring to ensure protocol adherence, maintain essential ... They may also support development of study-specific procedures (e.g., Monitoring Plans) and assist ...

Trice Healthcare

Clinical Research Informatician

Remote Duration: Direct Hire FTE Must Have's: * Bachelor's Degree in Health Information Management ... Clinical Research * Clinical Informatics * Information Technology and/or Academic Healthcare ...

New

New York University

Research Assistant

New York, NY · On-site +1

$29/hr

The research assistant will meet with the principal investigator on a weekly basis to discuss ... Remote Commitment: Temporary - Part-Time (10 hours/week) Start date: June 30, 2025 End date: August ...

Tribune Publishing

Research Assistant

Chicago, IL · Remote

$17.05/hr

This role is remote, but open to Illinois-based applicants only. What you will do: * Assist in fact ... Research assistants are encouraged to pitch ideas and write for various sections of the magazine ...

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Remote Clinical Research Assistant Volunteer information

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How much do remote clinical research assistant volunteer jobs pay per hour?

As of Aug 6, 2026, the average hourly pay for remote clinical research assistant volunteer in the United States is $22.71, according to ZipRecruiter salary data. Most workers in this role earn between $17.31 and $25.96 per hour, depending on experience, location, and employer.

What are the typical responsibilities of a remote clinical research assistant volunteer, and how is collaboration handled in a remote setting?

As a Remote Clinical Research Assistant Volunteer, your daily tasks often include data entry, managing study documentation, coordinating virtual meetings, and supporting regulatory compliance processes. Collaboration is typically managed through digital tools such as email, video conferencing, and shared project management platforms, ensuring you stay connected with research coordinators, investigators, and other team members. Clear communication and proactive updates are essential for staying aligned with the team despite the remote work environment. This role provides valuable exposure to clinical research operations while developing organizational and teamwork skills.

What is the difference between Remote Clinical Research Assistant Volunteer vs Remote Clinical Research Coordinator?

AspectRemote Clinical Research Assistant VolunteerRemote Clinical Research Coordinator
Required CredentialsTypically no formal certification; relevant coursework or experience helpfulOften requires certification or experience in clinical research
Work EnvironmentVolunteer role, often flexible, supporting research teams remotelyPaid position, managing study operations remotely or on-site
Employer & Industry UsageResearch institutions, universities, non-profitsPharmaceutical companies, research organizations, hospitals
Search & Comparison IntentUnderstanding volunteer opportunities in researchSeeking professional research coordination roles

The main difference is that a Remote Clinical Research Assistant Volunteer typically offers support without formal certification and is a volunteer role, whereas a Remote Clinical Research Coordinator is a paid position requiring more experience or certification, with greater responsibility in managing research studies.

What is a remote clinical research assistant volunteer?

Remote Clinical Research Assistant Volunteers are individuals who support clinical research projects from a remote location, typically assisting with tasks such as data entry, literature reviews, regulatory documentation, and communication with study participants or team members. Their work helps ensure that clinical studies are conducted efficiently and ethically, even if they are not physically present at the research site. Volunteers in this role often gain valuable experience in clinical research processes and contribute to important medical advancements, making it an excellent opportunity for those interested in the healthcare or research fields.

What are the key skills and qualifications needed to thrive as a remote clinical research assistant volunteer, and why are they important?

To thrive as a Remote Clinical Research Assistant Volunteer, you typically need a background in life sciences or healthcare, attention to detail, and basic knowledge of clinical research processes. Familiarity with data management systems, electronic data capture (EDC) tools, and Good Clinical Practice (GCP) certification is often required. Strong organizational skills, effective communication, and the ability to work independently are valuable soft skills in this remote role. These competencies ensure accurate data handling, regulatory compliance, and smooth collaboration within research teams, all of which are critical to successful clinical studies.
More about Remote Clinical Research Assistant Volunteer jobs
What cities are hiring for Remote Clinical Research Assistant Volunteer jobs? Cities with the most Remote Clinical Research Assistant Volunteer job openings:
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Remote Clinical Research Assistant Volunteer jobs near you
Infographic showing various Remote Clinical Research Assistant Volunteer job openings in the United States as of August 2026, with employment types broken down into 66% Full Time, 28% Part Time, and 6% Temporary. Highlights an 100% Remote job distribution, with an average salary of $47,241 per year, or $22.7 per hour.

Clinical Research Assistant

Allen Spolden

Silver Spring, MD • Remote

$45K - $55K/hr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 14 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