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Full Time Remote Clinical Research Jobs (NOW HIRING)

The Pennsylvania State University

$54K - $78K/yr

Approval of remote and hybrid work is not guaranteed regardless of work location.For additional ... full-time employees designed to support both personal and professional well-being. In addition to ...

Tilda Research

... various clinical research related tasks and requirements. Some understanding of basic medical ... Employment Type: FULL_TIME

Tufts Medicine

$26.50 - $35.25/hr

The Clinical Research Coordinator II will support participant recruitment, study operations, data collection, regulatory compliance, and participant retention across clinic-based and remote research ...

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Full Time Remote Clinical Research information

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$49K

$107.3K

$189K

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

As of Aug 9, 2026, the average yearly pay for full 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.

How do remote clinical research professionals typically collaborate with on-site teams and study sponsors?

Remote clinical research professionals often use a combination of digital communication tools such as video conferencing, project management platforms, and secure data-sharing systems to stay connected with on-site teams and sponsors. Regular virtual meetings help ensure alignment on study protocols, timelines, and regulatory requirements. While most tasks can be handled remotely, strong organizational and communication skills are essential for managing documentation, resolving queries, and maintaining study integrity. Successful remote collaboration relies on proactive engagement and clear, consistent reporting to all stakeholders.

What are the key skills and qualifications needed to thrive as a full time remote clinical research professional?

To excel in a Full Time Remote Clinical Research role, you need a solid background in life sciences or healthcare, experience with clinical trials, and typically a relevant degree such as a BSN, RN, or equivalent. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and certifications like GCP (Good Clinical Practice) are commonly required. Exceptional attention to detail, strong communication skills, and self-motivation are vital soft skills for remote coordination and data integrity. These competencies ensure accurate trial management, regulatory compliance, and effective collaboration in a remote environment.

What is a full time remote clinical research job?

A Full Time Remote Clinical Research job involves conducting, managing, or supporting clinical studies from a remote location, rather than working on-site at a hospital or research facility. Professionals in these roles may be responsible for tasks such as collecting and analyzing data, monitoring clinical trials, ensuring regulatory compliance, and communicating with study participants or teams virtually. This type of role allows for greater flexibility and the ability to work from anywhere with a reliable internet connection. Candidates typically need a background in life sciences or healthcare, strong organizational skills, and proficiency with digital communication and data management tools.

What is the difference between Full Time Remote Clinical Research vs Full Time Remote Clinical Data Coordinator?

AspectFull Time Remote Clinical ResearchFull Time Remote Clinical Data Coordinator
CredentialsTypically requires a degree in life sciences, healthcare, or related field; certifications like CCR or CCRA are commonRequires a degree in health informatics, data management, or related field; certifications like CDMP may be preferred
Work EnvironmentRemote, often involves collaboration with research teams, sponsors, and sitesRemote, focused on data entry, validation, and management within clinical trials
Industry UsageCommon in pharmaceutical, biotech, and CRO industriesPrimarily in clinical trial data management within similar industries

Full Time Remote Clinical Research roles involve overseeing clinical trial processes, ensuring compliance, and coordinating with multiple stakeholders. In contrast, Full Time Remote Clinical Data Coordinators focus on managing and validating trial data. Both roles are remote and industry-related but differ in responsibilities and required credentials.

More about Full Time Remote Clinical Research jobs
What cities are hiring for Full Time Remote Clinical Research jobs? Cities with the most Full Time Remote Clinical Research job openings:
What are the most commonly searched types of Remote Clinical Research jobs? The most popular types of Remote Clinical Research jobs are:
What states have the most Full Time Remote Clinical Research jobs? States with the most job openings for Full Time Remote Clinical Research jobs include:
What job categories do people searching Full Time Remote Clinical Research jobs look for? The top searched job categories for Full Time Remote Clinical Research jobs are:
Full Time Remote Clinical Research jobs near you
Infographic showing various Full Time Remote Clinical Research job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 71% Full Time, 18% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $107,336 per year, or $51.6 per hour.

Senior Clinical Research Associate

Icon plc

Blue Bell, PA • Remote

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 21 days ago

Job description

CRA II or Senior CRA-US-Remote

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.


As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.


ICON plc is seeking an experienced Senior Clinical Research Associate (Senior CRA) or Clinical Research Associate (CRA) to join our dynamic, collaborative team. In this role, you will be a key contributor to the successful execution of clinical trials, ensuring studies are conducted in full alignment with protocols, regulatory requirements, and industry standards. Your work will directly support data integrity, participant safety, and overall study excellence.

What You Will Be Doing:

  • Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.

  • Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.

  • Collaborating with investigators and site staff to facilitate smooth study conduct.

  • Performing data review and resolution of queries to maintain high-quality clinical data.

  • Contributing to the preparation and review of study documentation, including protocols and clinical study reports.

Your Profile:

  • Bachelor's degree in a scientific or healthcare-related field.

  • Minimum of 1-year independent monitoring to be considered for a Clinical Research Associate II and a minimum of 3 years independent monitoring to be considered for a Senior Clinical Research Associate.

  • In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.

  • Strong organizational and communication skills, with attention to detail.

  • Ability to work independently and collaboratively in a fast-paced environment.

  • Ability to travel at least 60% of the time (international and domestic - fly and drive) and should

#LI-JG1

#LI-Remote


Employment with ICON is contingent upon having the legal right to work in the country where the role is based.


Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.


Benefits may include:

  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.


Visit our careers site to read more about the benefits ICON offers.


Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.


If you require reasonable accommodations during the recruitment process, please let us know or submit a requesthere.

Are you a current ICON Employee? Please click here to apply

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