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Remote Radiation Therapy Jobs (NOW HIRING)

... emphasizing remote oversight and overall study quality. Responsibilities: * Monitors project ... Experience in Radiation Therapy or Radiopharmaceuticals, CAR-T Therapy or other types of Cell ...

... emphasizing remote oversight and overall study quality. Responsibilities: * Monitors project ... Experience in Radiation Therapy or Radiopharmaceuticals, CAR-T Therapy or other types of Cell ...

Senior Software Engineer, Adaptive

OR · Remote

$150K - $180K/yr

... radiation therapy efforts. The work sits at the intersection of medical imaging, geometric ... Fully remote work environment with virtual events and yearly retreats, because we like to have fun ...

Perform clinical research site activities, which can include onsite or remote monitoring, co ... radiation therapy conducted at the University of Oslo and Norway's Radium Hospital. Cancer is ...

Perform clinical research site activities, which can include onsite or remote monitoring, co ... radiation therapy conducted at the University of Oslo and Norway's Radium Hospital. Cancer is ...

It offers state-of-the-art Varian TrueBeam and Varian Edge radiation therapy technology at a nationally accredited Cancer Center. Its comprehensive offerings include an accredited Sleep Center ...

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Remote Radiation Therapy information

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$951

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$3.1K

How much do remote radiation therapy jobs pay per week?

As of Aug 16, 2026, the average weekly pay for remote radiation therapy in the United States is $2,016.25, according to ZipRecruiter salary data. Most workers in this role earn between $1,471.15 and $2,480.77 per week, depending on experience, location, and employer.

What is a remote radiation therapist?

A Remote Radiation Therapist is a healthcare professional who provides radiation treatment planning, consultation, or support services from a location outside of the physical clinic or hospital. Using secure telehealth platforms and digital tools, they collaborate with on-site teams to ensure patients receive precise and effective radiation therapy. This role allows for flexibility and can improve access to specialized care, especially in underserved areas. Remote Radiation Therapists maintain patient confidentiality and uphold high standards of safety and quality, just like their on-site counterparts.

What are the key skills and qualifications needed to thrive as a remote radiation therapist?

To thrive as a Remote Radiation Therapist, you need in-depth knowledge of radiation oncology, anatomy, and treatment planning, typically supported by a degree in radiation therapy and ARRT certification. Familiarity with remote treatment planning software, telemedicine platforms, and electronic medical records is essential for this role. Strong attention to detail, excellent communication, and the ability to work independently are important soft skills for remote collaboration with patients and clinical teams. These skills and qualifications are crucial to ensure accurate, safe, and effective cancer treatment delivery in a virtual environment.

What are some common challenges faced by remote radiation therapy professionals, and how can they be addressed?

One common challenge for remote radiation therapy professionals is ensuring seamless communication and coordination with on-site medical teams, as accurate treatment planning and patient safety depend on clear information exchange. Additionally, maintaining high data security standards when accessing sensitive patient records remotely is essential. To address these challenges, professionals often rely on secure telemedicine platforms, standardized protocols, and regular virtual meetings to stay connected and aligned with the broader care team.

What is the difference between Remote Radiation Therapy vs Radiation Therapist?

AspectRemote Radiation TherapyRadiation Therapist
CredentialsCertification in radiation therapy, ARRT certificationRadiation therapy certification, ARRT certification
Work EnvironmentRemote, often from home or telehealth settingsHospitals, clinics, cancer treatment centers
Employer & IndustryHealthcare providers offering remote servicesHospitals, outpatient clinics, cancer centers

Remote Radiation Therapy involves providing radiation treatment planning and consultation remotely, while Radiation Therapists operate equipment directly in clinical settings. The roles share certifications but differ mainly in work environment and daily tasks.

More about Remote Radiation Therapy jobs

What cities are hiring for Remote Radiation Therapy jobs?

Cities with the most Remote Radiation Therapy job openings:

What are the most commonly searched types of Radiation Therapy jobs?

The most popular types of Radiation Therapy jobs are:

What states have the most Remote Radiation Therapy jobs?

States with the most job openings for Remote Radiation Therapy jobs include:

Infographic showing various Remote Radiation Therapy 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 $104,845 per year, or $50.4 per hour.

Lead Clinical Research Associate

PSI CRO

Remote

Full-time

This job post has expired today. Applications are no longer accepted.


Job description

Company Description
We are the company that cares - for our staff, our clients, our partners, and the quality of the work we do.
Founded in 1995, PSI CRO is a privately owned, global Contract Research Organization with more than 3,000 employees dedicated to advancing medical science and bringing new therapies to patients worldwide.
In an industry shaped by mergers, acquisitions, and restructures, PSI stands apart. We have remained privately held, have never undergone a merger or acquisition, and have never experienced company-wide layoffs. Our long-term stability allows us to invest in our people, foster meaningful careers, and build lasting partnerships with our clients.
If you're looking for a collaborative organization where you can continue to grow while making a meaningful impact, PSI is the right place for you.
Job Description
As a Lead Clinical Research Associate, you'll provide leadership, oversight, and mentorship across regional clinical trials while partnering closely with Project Managers, Regional Project Leads, CRAs, and cross-functional teams to ensure high-quality study execution.
This role focuses on leadership, mentorship, oversight, and consistency in monitoring practices rather than direct site management, with minimal to no site assignments and a low-travel model, emphasizing remote oversight and overall study quality.
Responsibilities:
  • Monitors project timelines, patient enrollment, data cleaning, and ensuring compliance while implementing respective corrective and preventive measures.
  • Reviews monitoring visit reports for all visit types and ensures reporting compliance of the Monitors in the region.
  • Acts as the main communication line between Monitor, Site Management Associate, Regional Project Lead, and/ Project Manager.
  • Leads project team calls on a country level as well as provides status updates and reports to Regional Lead/ Project Manager.
  • Provides project-specific training and prepares training materials for the project team under supervision of a Project Manager and Regional Project Lead.
  • Supervises source data verification and follows up on data queries at site level in the country/region; reviews and manages study risks on a site level.
  • Ensures proper handling, use, accountability, reconciliation, and return of all Investigational Product(s) and clinical study supplies on a country/region level.
  • Reviews essential study documents and supervises reconciliation of study Investigator Site File (ISF) / TMF at site level and country/region level.
  • Ensures data integrity and compliance at a site level.
  • Collaborates with investigator/ site feasibility and identification process, as well as study startup.
  • Manages Monitors in the query resolution process, including Central Monitoring observations.
  • Coordinates safety information flow and protocol/process deviation reporting.
  • Performs clinical supplies management with vendors on a country and regional level.
  • Ensures study-specific and corporate tracking systems are updated in a timely manner.
  • Coordinates planning of supervised monitoring visits and conducts the visits.
  • Manages the project team in site contracting and payments.
  • Ensures ongoing evaluation of data integrity and compliance at a country/regional level.
  • Conducts site audit preparation visits, may participate in site audits, and coordinates resolution of site audit findings on a country/regional level.
  • Oversees project team in CAPA development and implementation.
  • Coordinates project team in process deviations review, management and reporting.
  • Conducts initial training and authorization monitoring visits for Monitors and acts as a mentor for newly promoted Lead CRAs.
  • Delivers trainings and presentations at Investigator Meetings.
  • Ensures that subject recruitment targets and project timelines are properly defined, communicated, recorded, and met at site level.
  • Ensures accurate and timely information flow with trial sites on Adverse Events and protocol/process deviations.
  • Supervises Site Management Associates in the flow of documents and laboratory supplies between the site and the Central/ Regional Lab/ Central Reviewer.
  • Supports preparation of draft regulatory and ethics committee submission packages.

Qualifications
  • Relevant educational background, such as MD, MPharm, RN or College/University degree in Life Sciences or an equivalent combination of education, training and experience.
  • Minimum of 4 years' site monitoring experience with participation in global clinical projects as a Lead Monitor or equivalent qualification level.
  • Experience with all types of monitoring visits in Phase II and/or III.
  • Strong experience in Oncology preferred.
  • Experience in Radiation Therapy or Radiopharmaceuticals, CAR-T Therapy or other types of Cell Therapy, Gene Therapy, or Nuclear Medicine is preferred.
  • Strong experience in GI (Chron's, Ulcerative Colitis, IBS) preferred.
  • Full working proficiency in English.
  • Proficiency in MS Office applications.
  • Ability to plan, multitask and work in a dynamic team environment.
  • Excellent Communication, collaboration, and problem-solving skills.
  • Ability to travel.
  • Valid driver's license (if applicable).

For this position PSI is not hiring individuals who require work visa for employment or continued employment now or anytime in the future.
Additional Information
Why Join PSI?
At PSI, we believe exceptional people deserve an exceptional workplace.
When you join PSI, you'll benefit from:
  • A stable, privately held CRO that has never undergone a merger or acquisition and has never experienced company-wide layoffs.
  • A unique leadership-focused CRA role with minimal travel and little to no routine site assignments.
  • Opportunities to mentor other CRAs and expand your leadership skills.
  • A collaborative, people-first culture where employees are genuinely supported.
  • Career development opportunities across a growing global organization.
  • The chance to contribute to innovative clinical research that improves patients' lives.