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Radiopharmaceutical Development Jobs (NOW HIRING)

Perspective Therapeutics

This role will involve close collaboration with multidisciplinary teams, including biologists, pharmacologists, and clinicians, to support the development of our radiopharmaceutical products while ...

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Radiopharmaceutical Development information

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$18K

$70.3K

$97K

How much do radiopharmaceutical development jobs pay per year?

As of Sep 13, 2026, the average yearly pay for radiopharmaceutical development in the United States is $70,347.00, according to ZipRecruiter salary data. Most workers in this role earn between $49,000.00 and $90,000.00 per year, depending on experience, location, and employer.

What is radiopharmaceutical development?

Radiopharmaceutical development is the process of designing, synthesizing, and testing radioactive compounds used for diagnosis or treatment in nuclear medicine. These compounds, called radiopharmaceuticals, are carefully engineered to target specific tissues or diseases within the body, such as cancer or neurological disorders. The development process involves multidisciplinary teams working in chemistry, biology, and medical imaging to ensure the safety and effectiveness of these drugs before they reach clinical use.

What are the key skills and qualifications needed to thrive in radiopharmaceutical development?

To excel in Radiopharmaceutical Development, you need a solid background in chemistry, pharmacology, and radiochemistry, typically supported by an advanced degree in a related scientific field. Familiarity with laboratory instrumentation, Good Manufacturing Practices (GMP), and regulatory compliance systems is essential. Strong problem-solving skills, attention to detail, and effective teamwork set top professionals apart. These competencies are crucial for ensuring the safe, effective, and compliant creation of radiopharmaceuticals for medical imaging and therapy.

What are some common challenges faced when working in radiopharmaceutical development, and how can they be managed?

Professionals in radiopharmaceutical development often encounter challenges such as strict regulatory requirements, handling short-lived radioactive materials, and ensuring product sterility. Managing these challenges requires meticulous attention to detail, adherence to safety protocols, and effective collaboration with multidisciplinary teams, including chemists, pharmacists, and regulatory specialists. Regular training, clear communication, and staying updated with industry standards are essential for maintaining a safe and productive work environment.

What is the difference between Radiopharmaceutical Development vs Radiopharmacist?

AspectRadiopharmaceutical DevelopmentRadiopharmacist
CredentialsAdvanced degrees in radiochemistry, pharmaceutical sciences, or related fieldsLicensed pharmacist with specialized training in radiopharmacy
Work EnvironmentResearch labs, pharmaceutical companies, clinical trial settingsHospitals, nuclear pharmacies, clinical settings
Industry UsageDrug development, formulation, and testing of new radiopharmaceuticalsPreparation, dispensing, and safety management of radiopharmaceuticals for patient use

Radiopharmaceutical Development focuses on creating and testing new radiopharmaceuticals in research and industry settings, while Radiopharmacists specialize in preparing and dispensing these drugs in clinical environments. Both roles require specialized knowledge but serve different stages of the radiopharmaceutical lifecycle.

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What cities are hiring for Radiopharmaceutical Development jobs?

Cities with the most Radiopharmaceutical Development job openings:

What states have the most Radiopharmaceutical Development jobs?

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What job categories do people searching Radiopharmaceutical Development jobs look for?

The top searched job categories for Radiopharmaceutical Development jobs are:

Radiopharmaceutical Development jobs near you
Infographic showing various Radiopharmaceutical Development job openings in the United States as of September 2026, with employment types broken down into 1% Internship, 1% As Needed, 81% Full Time, 15% Part Time, and 2% Contract. Highlights an 85% Physical, 3% Hybrid, and 12% Remote job distribution, with an average salary of $70,347 per year, or $33.8 per hour.

Sr Scientist - Radiopharmaceutical Development & CMC at Bristol Myers Squibb Indianapolis, IN

Indianapolis, IN • On-site

JIT Global Freight Solution P Ltd
See more jobs at JIT Global Freight Solution P Ltdexternal

$107K - $130K/yr

Other

Medical, Dental, Vision, Life, Retirement, PTO

Posted 11 days ago

Key responsibilities

  • Design, plan, and execute scientific experiments for pre‑clinical development of radiopharmaceuticals.

  • Drive CMC process development and optimization for clinical drug products, including formulation lock and process definition.

  • Support technology transfer of drug products and API from preclinical stage to clinical manufacturing.

Job description

Sr Scientist – Radiopharmaceutical Development & CMC – Bristol Myers Squibb

Location: Indianapolis, IN

Summary

We are seeking a highly motivated Sr. Scientist to lead the development and optimization of radiopharmaceutical drug products and radioisotopes. This position plays a pivotal role in driving preclinical development of innovative drug products aimed at treating various cancers and contributes to shaping and advancing our Chemistry, Manufacturing, and Controls (CMC) strategy.

Job Responsibilities
  • Design, plan and execute scientific experiments for pre‑clinical development of radiopharmaceuticals.
  • Drive CMC process development and optimization for clinical drug products, including formulation lock and robust process definition, ensuring scalability and compliance with regulatory standards.
  • Design, plan and execute scientific experiments for scale‑up and automation of drug products and API manufacturing processes.
  • Interpret complex experimental data, draw scientifically rigorous conclusions, and communicate findings in technical reports, regulatory documentation, and presentations for internal and external stakeholders.
  • Author technical reports and source documents to support regulatory filing.
  • Author CMC sections for IND/NDA for FDA submissions, and support regulatory filing in other jurisdictions such as EMA and Health Canada.
  • Support technology transfer of drug products and API from preclinical stage to clinical manufacturing.
  • Collaborate cross‑functionally with Regulatory, Quality, Supply Chain, Clinical, and R&D teams to ensure alignment with corporate goals.
  • Manage and prioritize research projects, oversee third‑party vendors, and mentor junior scientists and associates.
  • Provide support for commercialization of radiopharmaceuticals.
  • Up to 20% travel required.
Education and Experience
  • Ph.D., M.S., or B.S. in Chemistry, Chemical Engineering, Pharmaceutical Sciences, or a related field.
  • 5+ years of experience in drug development, manufacturing, CMC or related fields in a pharmaceutical industry, preferably radiopharmaceuticals.
Skills and Qualifications
  • Strong understanding of GMP, FDA/EMA regulations, and ICH guidelines.
  • Strong problem‑solving abilities and the ability to manage multiple projects in a fast‑paced environment.
  • Excellent project management and cross‑functional collaboration skills.
  • Excellent technical writing skills.
Physical Demands

While performing the duties of this job, the employee is regularly required to sit, reach with hands and arms, and talk or hear. The employee must occasionally lift and/or move up to 15 pounds. Specific vision abilities required by this job include close vision and distance vision. This position requires working in a laboratory environment; protective clothing, gloves, and safety glasses are required while working with radioactive materials.

Compensation Overview

Indianapolis – RayzeBio – IN: $107,904 – $130,754 (Full‑time employee). Additional incentive cash and stock opportunities (based on eligibility) may be available. Final compensation is determined based on demonstrated experience.

Benefits
  • Medical, pharmacy, dental, and vision care.
  • Well‑being support, employee assistance programs, financial well‑being resources, and 401(k).
  • Short‑ and long‑term disability, life insurance, supplemental health insurance, business travel protection, and survivor support.
  • Paid national holidays, optional holidays, Global Shutdown Days, up to 120 hours of paid vacation, 2 paid volunteer days, sick time off, and summer hours flexibility.
  • Parental, caregiver, bereavement, and military leave.
  • Family care services such as adoption and surrogacy reimbursement, fertility/infertility benefits, and other resources.
  • Tuition reimbursement and recognition program.
Equal Employment Opportunity

Bristol‑Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, pregnancy, citizenship, marital status, gender expression, genetic information, political affiliation, or any other characteristic protected by law.

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