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Vice President Radiopharmaceutical Jobs (NOW HIRING)

Telix Pharmaceuticals Limited

Develop and activate a globally coherent EVP and employer brand that is differentiated, authentic ... radiopharmaceutical sectors * Oversee executive search and strategic hiring initiatives for key ...

PHARMALOGIC HOLDINGS

$125K - $150K/yr

Vice President, Pharmacy Operations Job Overview: The Staff Nuclear Pharmacist (Floater) will play ... and radiopharmaceutical preparation and distribution. * Secure at least two (2) state licensure ...

Axcend, LLC

$110/hr

... DoD, radiopharmaceutical, chem/petrochem, oil/gas, academia, etc. We are expanding and have a ... Reporting to the VP, Sales, candidate develops and executes a sales plan to drive revenue growth ...

Clario

Medical Physicist

Performs image measurements of subject studies to provide radiopharmaceutical count data to be used ... Other responsibilities as assigned by the Vice President of Oncologic and Molecular Imaging ...

Clario

Sr. Medical Physicist

Performs image measurements of subject studies to provide radiopharmaceutical count data to be used ... Other responsibilities as assigned by the Vice President of Oncologic and Molecular Imaging ...

Clario

Sr. Medical Physicist

Performs image measurements of subject studies to provide radiopharmaceutical count data to be used ... Other responsibilities as assigned by the Vice President of Oncologic and Molecular Imaging ...

Clario

Medical Physicist

Performs image measurements of subject studies to provide radiopharmaceutical count data to be used ... Other responsibilities as assigned by the Vice President of Oncologic and Molecular Imaging ...

Telix Pharmaceuticals (AMER)

Senior Director, Global Talent

OR · On-site +1

$103K - $142K/yr

Develop and activate a globally coherent EVP and employer brand that is differentiated, authentic ... radiopharmaceutical sectors * Oversee executive search and strategic hiring initiatives for key ...

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How much do vice president radiopharmaceutical jobs pay per year?

As of Sep 13, 2026, the average yearly pay for vice president radiopharmaceutical in the United States is $157,532.00, according to ZipRecruiter salary data. Most workers in this role earn between $115,000.00 and $190,000.00 per year, depending on experience, location, and employer.

What does a vice president radiopharmaceutical do?

A Vice President of Radiopharmaceutical oversees the development, manufacturing, and commercialization of radiopharmaceutical products, which are used in medical imaging and cancer treatments. This executive role involves strategic planning, regulatory compliance, and collaboration with research, clinical, and business teams to drive product innovation and market growth. They also ensure that all operations meet safety and quality standards set by regulatory agencies while maintaining profitability and competitive advantage.

What are the key skills and qualifications needed to thrive as a vice president radiopharmaceutical?

To thrive as a Vice President, Radiopharmaceutical, you need advanced knowledge of pharmaceutical sciences, regulatory compliance, business strategy, and typically an advanced degree (PhD, PharmD, or MBA) in a relevant field. Expertise with Good Manufacturing Practices (GMP), FDA and EMA regulatory frameworks, and enterprise management systems is essential. Exceptional leadership, strategic thinking, and cross-functional communication enable effective team management and stakeholder engagement. These skills are critical for driving organizational growth, ensuring regulatory compliance, and leading innovation in a highly regulated and competitive industry.

What are some of the primary challenges faced by a vice president radiopharmaceutical, and how can candidates prepare to address them?

A Vice President of Radiopharmaceutical often faces challenges related to regulatory compliance, complex supply chain logistics, and driving innovation in a highly technical field. Candidates should be prepared to navigate strict FDA and international regulations, manage cross-functional teams including R&D, manufacturing, and commercial operations, and foster partnerships with healthcare providers. Staying updated on industry trends and building a strong network within the pharmaceutical and healthcare sectors are key steps toward success in this role.

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Cities with the most Vice President Radiopharmaceutical job openings:

What are the most commonly searched types of Radiopharmaceutical jobs?

The most popular types of Radiopharmaceutical jobs are:

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Vice President Radiopharmaceutical jobs near you
Infographic showing various Vice President Radiopharmaceutical job openings in the United States as of September 2026, with employment types broken down into 100% Full Time. Highlights an 100% Remote job distribution, with an average salary of $157,532 per year, or $75.7 per hour.

Sr. Director, CMC - Precursor Development & Manufacturing

Boston, MA • On-site

AdvanCell
See more jobs at AdvanCellexternal

$220K - $285K/yr

Other

Posted 7 days ago

Job description

The Sr. Director, CMC - Precursor Development & Manufacturing is responsible for the development, optimization, manufacturing, and lifecycle management of precursor molecules and related reference standards used in the Company's radiopharmaceutical products. This role provides technical leadership across synthetic chemistry, process development, analytical development, and GMP manufacturing of complex small molecules, including peptide-based and chelator-containing precursors.

The successful candidate will work closely with external contract development and manufacturing organizations (CDMOs) to build process understanding, support analytical method development and validation, and ensure alignment with global regulatory expectations (e.g., ICH, GMP). This work enables the timely delivery of high-quality drug substance and reference standards for clinical and commercial manufacturing. The Sr. Director also supports CDMO selection and shipping logistics for precursor materials.

The role also includes leading CMC regulatory writing and documentation to support regulatory submissions for precursors and related reference standards.


Key Responsibilities and Duties

  • Lead process development, optimization, and scale-up for precursor molecules and reference standards, including small molecules and peptide-based constructs

  • Provide subject matter expertise in synthetic organic and process chemistry, including route design, impurity control, and process robustness

  • Partner with the Associate Director of Analytical Development to guide analytical development activities and ensure methods are GMP-ready, fit for intended use, and capable of supporting manufacturing, release, and stability programs.

  • Ensure GMP-compliant manufacturing of precursor materials at CDMOs

  • Support technology transfer and scale-up activities for clinical and commercial manufacturing

  • Ensure CMC activities align with ICH guidelines and global regulatory requirements for drug substance development

  • Prepare and review CMC documentation for regulatory submissions (e.g., IND/CTA/MAA)

  • Partner with Quality Assurance on deviations, investigations, change controls, and audit readiness

  • Drive continuous improvement in process efficiency, robustness, and cost of goods

  • Support material specifications, control strategies, and impurity fate and purge assessments

  • Provide technical input to supply chain planning and risk mitigation strategies

  • Mentor and develop CMC staff and foster a strong technical culture

Other Responsibilities

  • Observe the Company's workplace, health and safety, and regulatory policies and procedures

  • Engage and communicate with other AdvanCell business unit staff to ensure that activities are coordinated seamlessly and effectively

  • Adhere to the Company's quality management system processes and policies

  • Other tasks as requested by the VP, CMC and Supply Chain

Essential Skills, Qualifications, Industry and Educational Requirements

  • Ph.D. in Chemistry (preferably Organic or Process Chemistry) or related discipline

  • Significant industry experience (typically 6+ years) in CMC, process development, or technical operations

  • Strong expertise in synthetic chemistry, including multi-step synthesis and impurity control

  • Working knowledge of analytical development and validation (e.g., HPLC, LC-MS, stability-indicating methods)

  • Advanced knowledge of GMP manufacturing and regulatory expectations

  • Strong understanding of ICH guidelines and global regulatory requirements

  • Demonstrated experience selecting and managing CDMOs and external partners

  • Excellent problem-solving, communication, and leadership skills

  • Ability to operate independently and effectively in a fast-paced, development-stage environment

  • Demonstrated ability to deliver to timelines in high-pressure environments

Desirable Skills, Qualifications, Industry and Educational Requirements

  • Experience in radiopharmaceutical or radiochemistry environments

  • Familiarity with chelator chemistry and metal complexation

  • Experience supporting regulatory submissions (e.g., IND/CTA/NDA/MAA)

  • Knowledge of CMC strategies for early- and late-phase development


$220,000 - $285,000 a year


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