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Associate Radiopharmaceutical Jobs in Dallas, TX

6630

Radiation Safety Technician

Dallas, TX

Associate's Degree in science related field or * High School Diploma. * Experience * No experience ... Performs radiation safety preparations in support of clinical radiopharmaceutical therapies (i.e ...

All JobsAssociate Radiopharmaceutical JobsAssociate Radiopharmaceutical Jobs in Dallas, TX

Associate Radiopharmaceutical information

See Dallas, TX salary details

$10

$19

$32

How much do associate radiopharmaceutical jobs pay per hour?

As of Aug 1, 2026, the average hourly pay for associate radiopharmaceutical in Dallas, TX is $19.65, according to ZipRecruiter salary data. Most workers in this role earn between $14.76 and $20.43 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as an Associate Radiopharmaceutical, and why are they important?

To thrive as an Associate Radiopharmaceutical, you need a solid background in chemistry or pharmacy, knowledge of radiopharmaceutical production, and a relevant degree or certification such as a bachelor's in pharmaceutical sciences or radiochemistry. Familiarity with laboratory safety procedures, Good Manufacturing Practice (GMP) standards, and specialized equipment like radioisotope generators is essential. Attention to detail, strong problem-solving abilities, and effective communication skills help ensure precise formulation and regulatory compliance. These skills are vital to maintain product safety, accuracy in dosing, and adherence to strict industry regulations.

What is an Associate Radiopharmaceutical?

An Associate Radiopharmaceutical is a professional who assists in the preparation, handling, and quality control of radioactive drugs used for diagnostic imaging and treatment in nuclear medicine. They work under the supervision of pharmacists, scientists, or physicians, ensuring that radiopharmaceuticals are prepared safely and accurately. Their responsibilities may include conducting laboratory tests, maintaining equipment, adhering to safety regulations, and documenting procedures. This role is crucial for supporting patient care and contributing to medical research involving radioactive substances.

What is the difference between Associate Radiopharmaceutical vs Radiopharmaceutical Technician?

AspectAssociate RadiopharmaceuticalRadiopharmaceutical Technician
CredentialsCertification in radiopharmacy, relevant courseworkCertification or training in radiopharmacy, limited formal education
Work EnvironmentHospitals, imaging centers, radiopharmacy labsHospitals, clinics, nuclear medicine departments
Job ResponsibilitiesPreparing, dispensing radiopharmaceuticals, quality controlAssisting in preparation, patient safety, inventory management

The Associate Radiopharmaceutical role typically involves more advanced responsibilities like preparing and quality controlling radiopharmaceuticals, often requiring specific certifications. Radiopharmaceutical Technicians focus on assisting with preparation and patient safety. Both roles work in similar environments and are essential in nuclear medicine departments, but the Associate Radiopharmaceutical generally has a higher level of training and responsibility.

What are some common challenges faced by Associate Radiopharmaceutical professionals in a clinical setting?

Associate Radiopharmaceutical professionals often encounter challenges such as adhering to strict safety and regulatory protocols when handling radioactive materials, maintaining accurate documentation, and ensuring the timely preparation and quality control of radiopharmaceuticals for patient procedures. Additionally, they must stay current with evolving technologies and regulatory requirements, which can require ongoing training. Collaboration with multidisciplinary teams—including pharmacists, nuclear medicine technologists, and physicians—is essential to ensure patient safety and workflow efficiency.
What are the most commonly searched types of Radiopharmaceutical jobs in Dallas, TX? The most popular types of Radiopharmaceutical jobs in Dallas, TX are:
What are popular job titles related to Associate Radiopharmaceutical jobs in Dallas, TX? For Associate Radiopharmaceutical jobs in Dallas, TX, the most frequently searched job titles are:
What job categories do people searching Associate Radiopharmaceutical jobs in Dallas, TX look for? The top searched job categories for Associate Radiopharmaceutical jobs in Dallas, TX are:
What cities near Dallas, TX are hiring for Associate Radiopharmaceutical jobs? Cities near Dallas, TX with the most Associate Radiopharmaceutical job openings:
Associate Radiopharmaceutical jobs near you
Infographic showing various Associate Radiopharmaceutical job openings in Dallas, TX as of July 2026, with employment types broken down into 1% As Needed, 75% Full Time, 22% Part Time, 1% Temporary, and 1% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $40,882 per year, or $19.7 per hour.

Associate Director, Regulatory Affairs - CMC

Orano

Plano, TX • On-site

Full-time

Posted 5 days ago

Job description

Description
Orano Med Theranostics
Orano Med has developed new processes for producing high-purity lead-212, a rare radioactive isotope. Lead-212 is currently at the heart of promising research projects in nuclear medicine to develop new treatments against cancer. The innovative approach, known as targeted alpha therapy (TAT), recognizes and destroys cancer cells while limiting the impact on nearby healthy cells.
The Associate Director, Regulatory Affairs - CMC will be responsible for leading the global regulatory CMC strategy for product development and registration, and for the preparation of CMC dossier in the expanding field of radiopharmaceuticals in the US and in EU.
This global role will join the regulatory team and will report directly to the Head of Regulatory Affairs. The person will work cross-functionally with the CMC team and the manufacturing sites to lead the regulatory CMC strategy and the preparation of regulatory CMC documentation and submissions in adherence to relevant regulatory requirements and company standards.
Key Responsibilities:
  • Leads the development and preparation of global (US and EU) CMC-related submission documents for the pipeline of radiopharmaceutical products. This includes authoring, review and consolidation to deliver high-quality documents. Working in close collaboration with the CMC team (Manufacturing, Quality, R&D process), the regulatory CMC lead will collect technical data from relevant partners to write regulatory CMC documents and support the overall project goals.
  • Develops robust global regulatory CMC strategies for the pipeline of radiopharmaceutical products. Identifies risks and proposes risk mitigation to enable successful regulatory submissions and approvals. Aligns within Regulatory Affairs to enable one regulatory voice.
  • The regulatory submissions include but are not limited to the M3/CMC section of INDs/CTAs (IMPD-Q), DMF/ASMF, briefing documents, response to queries, Orphan Drug Applications, and annual reports.
  • Manages regulatory CMC agency interactions and meetings.
  • Meets current regulatory standards and achieves timely submissions, to enable approval on the first review cycle. Effectively interprets and applies regulatory CMC guidance. Provides recommendations and solutions to cross-functional teams and key stakeholders.
  • Works with the Regulatory Operations vendor to coordinate publishing and submission for CMC dossiers (eCTD)
  • Leads or contributes to the development of internal processes to improve the regulatory and CMC ways of working.
  • Remains current on CMC regulatory intelligence.

Requirements
All candidates must meet the following minimum requirements in order to be considered for this opportunity. Candidates who exceed minimum qualifications may be considered for a higher-level position.
Minimum Qualifications:
  • Bachelor's degree in a scientific discipline. Advanced degree (MS, PharmD or PhD) is a plus.
  • A minimum of 8 years Regulatory CMC experience and/or CMC technical writing experience in a pharmaceutical or biotechnology environment including injectables.

Required Skills and Competencies:
  • Demonstrated hands-on experience in pharmaceutical development, registration in the US and/or EU, and interaction with health authorities. Demonstrated experience in preparing regulatory submissions, including IND/CTA, NDA/MAA, DMF/ASMF, briefing documents, and response to agency questions.
  • Technical knowledge in small molecules with experience in translating to a regulatory document. Knowledge of radiopharmaceuticals and innovative platforms is a plus.
  • Knowledge of relevant global CMC regulations and guidelines (ICH, US, EU)
  • Experience within a GMP environment with a firm understanding of industry regulations and best practices
  • Ability to understand and interpret complex scientific issues across multiple projects as it relates to regulatory requirements and strategy.
  • Excellent verbal and written communication skills. Able to defend the regulatory CMC position while maintaining positive professional relationships
  • Proactive, able to work independently and collaboratively in a fast-paced emerging field
  • Analytical thinker with good problem-solving skills and the capacity to adapt to a field with relatively few guidelines available.
  • Excellent planning and organization skills including the ability to support multiple projects.
  • Proficiency with Microsoft Office.
  • Travel requirements: Up to 10% travel

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