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Remote Clinical Research Monitor Jobs in Oregon (NOW HIRING)

Natera

Senior Clinical Research Associate

OR · On-site +1

The Senior Clinical Research Associate is responsible for the overall operational execution of ... Monitor and track clinical trial progress, provide status updates to stakeholders * Develop new ...

Care Access

Region Manager

OR · On-site +1

$95K - $115K/yr

Oversee day-to-day operations at multiple clinical research sites within the region. * Ensure ... Lead all phases of clinical trial execution including site initiation, monitoring, subject ...

Natera

Senior Manager, Clinical Trials

OR · On-site +1

Monitor and track clinical trial progress and provide status update to stakeholders. * Partner with other research and development groups to achieve deliverables. * This role works with PHI on a ...

Natera

Senior Clinical Scientist, ECD

OR · On-site +1

San Carlos, CA or Remote, USA (West Coast or Mountain time zones preferred) PRIMARY ... Actively monitor study conduct, enrollment performance, protocol compliance, and clinical data ...

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Remote Clinical Research Monitor information

What is the difference between Remote Clinical Research Monitor vs Clinical Research Associate?

AspectRemote Clinical Research MonitorClinical Research Associate
CredentialsTypically requires a degree in life sciences, nursing, or related field; certifications like CCRP or RAC are commonSimilar credentials; often holds degrees in health sciences and certifications such as CCRP
Work EnvironmentPrimarily remote, overseeing multiple sites remotelyCan be on-site or remote, depending on the study phase and sponsor
Industry UsageUsed across pharmaceutical, biotech, and CROs for remote monitoring rolesCommonly employed in clinical trial sites and CROs for site management

Both roles require similar educational backgrounds and certifications. The main difference lies in the work environment: Remote Clinical Research Monitors work mainly remotely overseeing multiple sites, while Clinical Research Associates may work on-site at trial locations or remotely. Both roles are vital in clinical trials and often overlap in responsibilities, but their work settings and focus differ slightly.

What are the most commonly searched types of Clinical Research Monitor jobs in Oregon?

The most popular types of Clinical Research Monitor jobs in Oregon are:

What are popular job titles related to Remote Clinical Research Monitor jobs in Oregon?

For Remote Clinical Research Monitor jobs in Oregon, the most frequently searched job titles are:

What job categories do people searching Remote Clinical Research Monitor jobs in Oregon look for?

The top searched job categories for Remote Clinical Research Monitor jobs in Oregon are:

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Remote Clinical Research Monitor jobs near you

Senior Clinical Research Associate

Icon plc

Portland, OR • Remote

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 27 days ago

Job description

Senior CRA / CRA II - United States - Home Based

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.


As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.

What You Will Do:

You will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement.
Key responsibilities include:

  • Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
  • Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
  • Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting.
  • Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.
  • Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.

Your Profile:

You will have a strong foundation in clinical trial monitoring, with the experience to work independently and guide others.
Required qualifications and experience:

  • Bachelor's degree in a relevant scientific discipline or healthcare-related field
  • Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.
  • Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills.
  • Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.
  • Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment.
  • Willingness to travel as required (approximately 60%)

    #LI-LB1 #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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