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Telix Pharmaceuticals

Develops targeted radiation diagnostics and therapies

Manager, Regulatory Affairs - Operations

Regulatory & Quality (Life Sciences)Posted on Nov 11
Full-timeRemote in USA

About the Job

Requirements

  • A bachelor's degree or equivalent experience is required.
  • At least 7 years of experience in Regulatory Affairs Operations is required.
  • Experience preparing regulatory submission documents, including formatting, quality control, submission-ready preparation, and finalization of regulatory documents for electronic Common Technical Document submissions, such as New Drug Applications or European Union Marketing Authorization Applications.
  • Strong organizational skills and the ability to manage multiple projects and deadlines are required.
  • Excellent attention to detail and accuracy in documentation are required.
  • Expert knowledge of Common Technical Document and electronic Common Technical Document structure, format, and submission requirements, including Lorenz docuBridge, is required.
  • Experience with Microsoft Word, including authoring templates, Adobe Acrobat, electronic publishing software, and document management systems such as CSC Toolbox and Veeva Collaborative Authoring or equivalent is required.
  • Strong project management skills and the ability to assess and advise teams on potential impacts or changes in project timelines are required.
  • Strong written and verbal communication skills, including the ability to communicate effectively with internal colleagues at various levels and external vendor partners, are required.
  • The ability to work independently in a remote setting across multiple time zones as needed, build relationships, and work effectively in a team environment is required.
  • Fluency in spoken and written English is required.

Responsibilities

  • Collaborate with teams to guide regulatory requirements and expectations for preparing compliant submission documents, including managing document workflows for timely deliverables.
  • Work within submission plans, manage submission document preparation deadlines across the product portfolio, and coordinate activities between relevant functions.
  • Stay current on industry trends relevant to global electronic submissions and document preparation for electronic Common Technical Document submissions.
  • Participate as needed in maintaining Regulatory Information Management Systems and electronic document management systems, including Veeva Submission and Archive Vaults.
  • Understand electronic Common Technical Document publishing systems, including Lorenz docuBridge, and publish-readiness requirements defined by the industry and company.
  • Develop and manage document preparation processes using templates and internal style guides to ensure quality control and formatting standardization.
  • Support and enhance regulatory operations document infrastructure by refining procedures, standards, templates, and style guides for authoring, formatting, reviewing, and publishing submission documents.
  • Provide internal teams with guidance on document-related best practices and regulatory requirements, and troubleshoot or train as needed.
  • Improve business processes for preparing documents for regulatory submission by establishing procedures where needed and upholding quality standards.
  • Assist Regulatory Operations management with administrative and compliance tasks, including facilitating Health Authority portal submissions, overseeing internal Regulatory Affairs statement-of-work and purchase-order system administration, and generating metric reports for leadership.

Desired Qualifications

  • Preferred experience with United States, Canadian, and/or European regulatory legislation and procedures.
  • A general understanding of dossier Life Cycle Management is desired.
  • An additional European language is an asset.

About the Company

Telix Pharmaceuticals

Develops targeted radiation diagnostics and therapies

Telix Pharmaceuticals develops and commercializes diagnostic and therapeutic products that use targeted radiation to diagnose and treat cancer and rare diseases. Its pipeline covers urologic oncology (prostate and kidney cancers), neuro-oncology (glioma), musculoskeletal oncology (sarcoma), and bone marrow conditioning. The treatments work by delivering targeted radiation to diseased tissues, enabling more precise decisions for treatment and allowing for personalized therapy. The company differentiates itself through a global, robust supply chain and a focus on integrating diagnostic and therapeutic options to address unmet medical needs, along with strong commitments to patient care, ethical practices, and environmental responsibility. Telix’s goal is to improve quality of life and outcomes for patients by providing targeted, clinically meaningful diagnostic and therapeutic solutions that support better treatment decisions and personalized care.

Company size
1,001-5,000
Company stage
IPO
Headquarters
Melbourne VIC, Australia
Founded
2015

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