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Remote Cra 1 Jobs (NOW HIRING)

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CRA II

Blue Bell, PA · Remote

Minimum of 1 year independent monitoring to be considered for a Clinical Research Associate II and ... ZH1 #LI-REMOTE Employment with ICON is contingent upon having the legal right to work in the ...

410 ICR United States USA

CRA II

Blue Bell, PA · Remote

Minimum of 1 year independent monitoring to be considered for a Clinical Research Associate II and ... ZH1 #LI-REMOTE Employment with ICON is contingent upon having the legal right to work in the ...

Emmes

Sr. In-House CRA

Rockville, MD · On-site +1

Overview Sr. In-House CRA Be Part of One Team, One Purpose. At Emmes Group , we're shaping the ... May perform remote review and monitoring of Informed Consent Forms and other source documents.

Emmes

Clinical Research Associate II

Rockville, MD · On-site +1

... CRA, Project Manager, etc., independently schedules and conducts remote and on-site monitoring ... One Team, One Purpose. Why work at Emmes? At Emmes, your actions and hard work will have a direct ...

Emmes

Clinical Research Associate II

Rockville, MD · On-site +1

Emmes Group was founded as Emmes more than 47 years ago, becoming one of the primary clinical ... CRA, Project Manager, etc., independently schedules and conducts remote and on-site monitoring ...

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Remote Cra 1 information

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$11K

$79.4K

$137.5K

How much do remote cra 1 jobs pay per year?

As of Sep 10, 2026, the average yearly pay for remote cra 1 in the United States is $79,437.00, according to ZipRecruiter salary data. Most workers in this role earn between $33,000.00 and $136,500.00 per year, depending on experience, location, and employer.

What is the difference between Remote Cra 1 vs Remote Clinical Research Associate?

AspectRemote Cra 1Remote Clinical Research Associate
CredentialsBachelor's degree, relevant certifications often preferredBachelor's degree, certifications like ACRP or SOCRA beneficial
Work EnvironmentRemote, office-based or site visits as neededPrimarily remote, with site visits and monitoring
Industry UsageCommon entry-level role in clinical trialsBroader term, includes various experience levels
Job ResponsibilitiesMonitoring, data review, site communicationMonitoring, regulatory compliance, data management

Remote Cra 1 is typically an entry-level position focusing on clinical trial monitoring and data review, often requiring a bachelor's degree and relevant certifications. Remote Clinical Research Associate is a broader term that includes various experience levels but generally involves similar responsibilities. The main difference lies in the experience level and specific job scope, with Remote Cra 1 being more junior and entry-level.

What cities are hiring for Remote Cra 1 jobs?

Cities with the most Remote Cra 1 job openings:

What are the most commonly searched types of Cra 1 jobs?

The most popular types of Cra 1 jobs are:

What states have the most Remote Cra 1 jobs?

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Remote Cra 1 jobs near you

CRA II

Blue Bell, PA • Remote

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See more jobs at Icon plcexternal

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 20 days ago

Job description

Senior CRA/ CRA II

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.


We are currently seeking a Senior Clinical Research Associate or Clinical Research Associate II to join our diverse and dynamic team. As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.

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 health-related field or an equivalent combination of education and clinical research experience, particularly in a study coordinator or nursing role

  • 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 possess a valid driver's license

#LI-ZH1

#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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