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Full Time Radiopharmaceutical Jobs (NOW HIRING)

Shift: Full-Time | Monday to Friday | 12 AM-8 AM Job Summary The Nuclear Technologist supports the preparation, handling, dispensing, packaging, and distribution of radiopharmaceutical products ...

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Full Time Radiopharmaceutical information

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$50K

$87.7K

$143.5K

How much do full time radiopharmaceutical jobs pay per year?

As of Sep 13, 2026, the average yearly pay for full time radiopharmaceutical in the United States is $87,706.00, according to ZipRecruiter salary data. Most workers in this role earn between $65,500.00 and $100,000.00 per year, depending on experience, location, and employer.

What is the difference between Full Time Radiopharmaceutical vs Full Time Radiologic Technologist?

AspectFull Time RadiopharmaceuticalFull Time Radiologic Technologist
CredentialsCertification in Nuclear Medicine Technology (CNMT), state licensureARRT certification in Radiography, state licensure
Work EnvironmentHospitals, imaging centers, nuclear medicine departmentsHospitals, clinics, outpatient imaging centers
Job DutiesPreparing and administering radiopharmaceuticals, patient care, imagingPerforming X-rays, CT scans, patient positioning

Full Time Radiopharmaceuticals focus on preparing and administering radiopharmaceuticals for imaging and therapy, requiring specialized nuclear medicine certifications. Full Time Radiologic Technologists operate imaging equipment like X-rays and CT scans. Both roles work in healthcare settings but have distinct responsibilities and certification requirements.

What cities are hiring for Full Time Radiopharmaceutical jobs?

Cities with the most Full Time Radiopharmaceutical job openings:

What are the most commonly searched types of Radiopharmaceutical jobs?

The most popular types of Radiopharmaceutical jobs are:

CRAs & Sr. CRAs - Radiopharmaceutical Therapies - Remote US

OR • On-site, Remote

Fortrea
Health Care and Social Assistance • 10K+ employees

$105/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 29 days ago


Key responsibilities

  • Perform all aspects of study site monitoring, including routine monitoring, close-out, and maintenance of study files.

  • Ensure study staff are properly trained and that patient protection and protocol adherence are maintained, including informed consent procedures.

  • Complete data review, query resolution, SAE reporting, and assist with training and coordination of clinical projects.


Fortrea rating

8.3

Company rating: 8.3 out of 10

Based on 11 frontline employees who took The Breakroom Quiz


Job description

We are currently seeking Experienced CRAs with Radiopharmaceutical therapeutic expertise to lead and support our Full Service Outsourcing team working with various sponsors. 1+ year of independent CRO/sponsor monitoring required. Open to major hub locations across the US. 60-70% travel, 8-10 DOS per month.

WHAT YOU WILL DO

You will utilize your skills, knowledge, and clinical judgement to provide a high standard of care for participants in clinical trials and respond to emergency situations based upon clinical research standards.

Responsibilities:

  • Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned -
  • Responsible for all aspects of site management as prescribed in the project plans
  • General On-Site Monitoring
  • Ensure the study staff who will conduct the protocol have received the proper materials and instructions to safely enter patients into the study
  • Ensure the protection of study patients by verifying that informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirements
  • Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document Monitor data for missing or implausible data
  • Responsible for all aspects of registry management as prescribed in the project plans - Undertake feasibility work when requested
  • Complete Serious Adverse Event (SAE) reporting, process production of repo11s, narratives and follow up of SAEs
  • Independently perform CRF review; query generation and resolution against established data review guidelines on Fortrea or client data management systems as assigned by management
  • Assist with training of new employees, eg. co-monitoring
  • Coordinate designated clinical projects as a Local Project Coordinator (with supervision, ifapplicable) and may act as a local client contact as assigned
  • Perform other duties as assigned by management

Requirements

  • University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g. nursing licensure)
  • 1+ years of Clinical Monitoring experience
  • Radiopharmaceutical experience is desired
  • Open to various hub locations

The important thing for us is you are comfortable working in an environment that is:

  • Fast paced: where no deviations from the study protocol are allowed, and not meeting a timeline for even few minutes will create a quality issue.
  • Changing priorities constantly asking you to prioritize and adapt on the spot.
  • Teamwork and people skills are essential for the study to run smoothly.
  • Technology based. We collect our data directly into an electronic environment.

What do you get?

Regular, full-time or part-time employees working 20 or more hours per week are eligible for comprehensive benefits including but not limited to:

  • Medical, Dental, Vision, Life, STD/LTD (multiple insurance carriers)
  • 401(K)
  • Paid time off (PTO) - Flex Plan
  • Employee recognition awards
  • Multiple ERG's (employee resource groups)
  • Target Pay Range (based on title): $105-145K

Work Environment:

  • Work is performed in an office environment with exposure to electrical office equipment.
  • Frequent travel to clients/ site locations with occasional travel both domestic and international.

Physical Requirements:

  • Ability to sit for extended periods and operate a vehicle safely.
  • Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists.
  • Occasional crouching, stooping, with frequent bending and twisting of upper body and neck.
  • Ability to access and use a variety of computer software developed both in-house and off-the-shelf.
  • Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs.
  • Regular and consistent attendance.
  • Varied hours may be required.

#LI - Remote

Applications will be accepted on an ongoing basis.

Learn more about our EEO & Accommodations request here.


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