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Flex Time Remote Clinical Research Jobs (NOW HIRING)

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 ...

WEP Clinical

Senior Clinical Research Associate

They conduct on-site and remote monitoring to ensure protocol adherence, maintain essential ... time Paid maternity & paternity leave What Sets Us Apart: WEP Clinical partners with ...

Compass Group

Remote Clinical Dietitian

Time Off - Flexible/Paid Time Off and holiday pay (varies by site/state), Paid Parental Leave ... Apply the latest research in alignment with the diet manual, company policies, and facility ...

IQVIA

Clinical Research Coordinator

Raleigh, NC · Remote

$35 - $42/hr

This position is not eligible for employment sponsorship. #LI-CES and #LI-DNP #LI-HCP #remote IQVIA is a leading global provider of clinical research services, commercial insights and healthcare ...

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$49K

$107.3K

$189K

How much do flex time remote clinical research jobs pay per year?

As of Aug 15, 2026, the average yearly pay for flex time remote clinical research in the United States is $107,336.00, according to ZipRecruiter salary data. Most workers in this role earn between $81,000.00 and $122,500.00 per year, depending on experience, location, and employer.

What is the difference between Flex Time Remote Clinical Research vs Part-Time On-Site Clinical Research Coordinator?

AspectFlex Time Remote Clinical ResearchPart-Time On-Site Clinical Research Coordinator
Work EnvironmentRemote, flexible hoursOn-site, fixed hours
CredentialsTypically requires clinical research experience and certificationsSimilar credentials, often including CRC certification
Employer & IndustryPharmaceutical companies, CROs, research institutionsHospitals, clinics, research sites
Search & Comparison IntentFlexibility, remote work optionsOn-site responsibilities, part-time schedule

Flex Time Remote Clinical Research roles offer flexible, remote work environments requiring similar credentials as on-site coordinators. In contrast, Part-Time On-Site Clinical Research Coordinators work at research sites with fixed hours. Both roles involve managing clinical trials but differ mainly in location and scheduling flexibility.

More about Flex Time Remote Clinical Research jobs

What cities are hiring for Flex Time Remote Clinical Research jobs?

Cities with the most Flex Time Remote Clinical Research job openings:

What states have the most Flex Time Remote Clinical Research jobs?

States with the most job openings for Flex Time Remote Clinical Research jobs include:

What job categories do people searching Flex Time Remote Clinical Research jobs look for?

The top searched job categories for Flex Time Remote Clinical Research jobs are:

Flex Time Remote Clinical Research jobs near you
Infographic showing various Flex Time Remote Clinical Research job openings in the United States as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% Remote job distribution, with an average salary of $107,336 per year, or $51.6 per hour.

Clinical Research Assistant

Allen Spolden

Silver Spring, MD • Remote

$45K - $55K/hr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 23 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