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International Clinical Research Remote Jobs (NOW HIRING)

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 ...

St Joseph Hospital & Medical Center

$35.62 - $52.99/hr

Effective long-term planning/scheduling of remote and on-site monitoring visits in accordance with ... Bachelors Degree or equivalent combination of education and experience or its international ...

Novartis

$108K - $201K/yr

Senior Clinical Research Associate (Sr. CRA) #LI-Remote (Field Based) Primary Location: Florida ... The expectation of working hours and travel (domestic and/or international) will be defined by the ...

Essentia Health

Clinical Research Assistant

Duluth, MN · On-site +1

$18.69 - $27.85/hr

Experience in oncology, clinical research, academic research or similar area. Over 1 year computer ... None FTE: 1 Possible Remote/Hybrid Option: Shift Rotation: Day Rotation (United States of America ...

Hanger, Inc.

Director of Clinical Research

$140K - $150K/yr

The Director of Clinical Research will serve within Hanger's Department of Clinical and Scientific ... Remote: Pay range of $140,000- $150,000 + bonus + benefits. This pay range is posted to comply with ...

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International Clinical Research Remote information

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$49K

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$189K

How much do international clinical research remote jobs pay per year?

As of Aug 7, 2026, the average yearly pay for international clinical research remote 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 international clinical research remote work?

International clinical research remote work involves overseeing or supporting clinical trials and studies conducted in multiple countries, while working from a location outside of a traditional office or clinical site. Professionals in this field coordinate research activities, ensure regulatory compliance, manage data, and communicate with international teams—all through digital platforms. This approach allows for greater flexibility and collaboration across borders, but also requires strong organizational and communication skills to handle complex, multi-site research projects.

Is a clinical research associate an entry level job?

A clinical research associate (CRA) is often an entry-level position, especially for those with a bachelor's degree in a related field. However, some roles may require prior experience or certifications, such as GCP training, and responsibilities can vary depending on the company and project complexity.

What are some common challenges faced by remote international clinical research professionals, and how can they be addressed?

Remote international clinical research professionals often encounter challenges such as coordinating across multiple time zones, managing effective communication with diverse teams, and ensuring compliance with varying regulatory requirements. Addressing these challenges typically involves leveraging project management and collaboration tools, establishing clear communication protocols, and staying updated on country-specific clinical trial regulations. Proactive planning and adaptability are key, as is fostering strong relationships with both local site teams and global colleagues.

What is the difference between International Clinical Research Remote vs Clinical Research Coordinator?

AspectInternational Clinical Research RemoteClinical Research Coordinator
CredentialsTypically requires clinical research certifications, such as CCRP or CCRCOften requires similar certifications, plus site-specific training
Work EnvironmentRemote, often international, flexible hoursOn-site or local site-based, regular hours
Employer & Industry UsagePharmaceutical companies, CROs, research institutionsHospitals, clinics, research sites
Search & Comparison IntentRemote international roles, global clinical research jobsLocal site management, patient coordination roles

International Clinical Research Remote roles focus on managing clinical trials remotely across borders, requiring strong communication skills and certifications. Clinical Research Coordinators typically work on-site at research sites, coordinating patient visits and data collection. Both roles share certifications but differ mainly in work environment and location.

What are the key skills and qualifications needed to thrive as an international clinical research professional working remotely, and why are they important?

To thrive as an International Clinical Research professional working remotely, you need a strong background in life sciences, clinical trial management, and regulatory compliance, often supported by a degree in a related field and experience in global studies. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and certifications such as GCP (Good Clinical Practice) are typically required. Exceptional organizational skills, cross-cultural communication, and self-motivation are vital soft skills for collaborating with global teams and managing complex projects remotely. These skills and qualifications ensure regulatory adherence, data integrity, and effective coordination across international research sites.
More about International Clinical Research Remote jobs
What cities are hiring for International Clinical Research Remote jobs? Cities with the most International Clinical Research Remote job openings:
What are the most commonly searched types of International Clinical Research jobs? The most popular types of International Clinical Research jobs are:
What states have the most International Clinical Research Remote jobs? States with the most job openings for International Clinical Research Remote jobs include:
What job categories do people searching International Clinical Research Remote jobs look for? The top searched job categories for International Clinical Research Remote jobs are:
International Clinical Research Remote jobs near you
Infographic showing various International Clinical Research Remote job openings in the United States as of August 2026, with employment types broken down into 82% Full Time, 9% Part Time, and 9% Temporary. Highlights an 100% Remote job distribution, with an average salary of $107,336 per year, or $51.6 per hour.

Senior Clinical Research Associate - CNS

Cognitive Research Corporation

Remote

Full-time

Re-posted 8 hours ago

Job description

The Senior Clinical Research Associate is responsible for overseeing the execution of clinical trials at Investigative Sites. The Clinical Research Associate acts as a liaison between the study Sponsor, CRC and Investigative Sites. They will proactively identify and resolve clinical project issues and participate in process improvement initiatives as applicable. The CRA facilitates successful execution of studies by Investigative Sites and helps to ensure the rights, safety and welfare of human research participants as well as data integrity in clinical trials.
Essential Duties & Responsibilities
  • Initiates, monitors, and closes-out investigative sites in accordance with FDA/ICH regulations.
  • Tracks and maintains study specific non-Case Report Form database
  • Administers Clinical research projects; collects investigator documentation, site management, clinical contact, and prepare reports as required
  • Ensures appropriate source document review and source document verification as required
  • Reviews Case Report Forms to identify erroneous, missing, or incomplete data
  • Generates queries to resolve problematic data to appropriate personnel, and review responses to assure the database is updated accordingly
  • Verifies study drug accountability; generates and tracks drug shipments and storage
  • Travels as necessary, based on project needs and according to Clinical Monitoring Plan requirements
  • Performs data collection, retrieval, entry and clean up as necessary
  • Develops and maintains strong relationships with Investigator(s) and site staff
  • Independently manages sites resulting in acceptable Quality Assurance reports.
  • Escalates study/site issues/deviations appropriately
  • Serves as lead monitor for a protocol or project by creating study files, arranges monitoring schedules, leads the project team, organize and run meetings and performs other project management duties as assigned by management
  • Writes Clinical Trial Reports, analyzing and presenting trial results in a clear and accurate format
  • Reports, writes narratives, and follows-up on reported serious adverse events
  • Interacts and attends client meetings, as appropriate
  • Mentors junior staff/CRAs
  • Quality oversight checks of monitoring
  • Performs other duties as assigned

Qualifications
  • Bachelor's degree, or RN, in a related field or equivalent combination of education, training and experience
  • Minimum 5 years' experience as a CRA; experience overseeing clinical trials in the pharmaceutical, hospital or CRO industry
  • Ability to work and travel independently with minimal supervision
  • Experience with numerous EDC systems.
  • Advanced knowledge of GCPs, ICH guidelines, FDA and other applicable regulations
  • Specialized knowledge of CNS therapeutic areas
  • Proficiency in Microsoft Office, Zoom and Adobe
  • Excellent writing and verbal skills, English language proficiency
  • Meticulous attention to detail
  • Time management and ability to prioritize tasks
  • Ability to travel up to 70%

Department Clinical Operations Role Senior Clinical Research Associate Locations Remote, US Remote status Fully Remote Employment type Full-time

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