Telix Pharmaceuticals Limited

Senior Specialist, Medical Communications – Scientific Publications

Telix Pharmaceuticals Limited

full-time

Posted on:

Location Type: Remote

Location: United States

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Job Level

Senior

About the role

  • Supporting the execution of the scientific publications and communications plan
  • Developing medical writing and communications deliverables including slide decks and scientific manuscripts (eg, clinical trials results, real world evidence, health economics outcomes, literature reviews)
  • Working closely with authors, key opinion leaders, and internal stakeholders
  • Leading the overall development process (eg, performing lit reviews / background research; drafting outline and multiple draft iterations; collecting, collating, and incorporating author / reviewer comments)
  • Collaborating cross functionally in partnership with internal teams (e.g., Clinical Science, Clinical Operations, Product Portfolio/Global Commercial, Research & Innovation, Marketing, Market Access, Intellectual Property, Medical Information and Pharmacovigilance Teams) to drive corporate objectives across the organization.

Requirements

  • Advanced degree in a scientific concentration and relevant experience: Master’s degree in a with 4+ years or PhD (preferred) with 2+ years relevant experience required.
  • 5+ years’ experience with publications (e.g., peer-reviewed manuscripts, abstracts, and related poster/oral presentations). Industry and/or pharmaceutical experience required
  • 2+ years of Oncology, health economical outcomes research, and/or real-world evidence research experience is a plus
  • Medical editing and quality review of scientific publications experience required (ex: regulatory, manuscripts, abstracts, etc.).
  • Working knowledge of current publication environment and relevant standards / documents (eg, ICMJE Authorship Guidelines, Good Publication Practice guidelines, AMA manual of style, EQUATOR reporting guidelines).
  • Ability to critically read, interpret, and communicate knowledge from scientific literature including peer-reviewed manuscripts and regulatory documents (e.g., protocol, investigator's brochure, clinical study report).
  • Highly skilled with using Microsoft PowerPoint, Word, Excel, and reference managers. Experience with EndNote, visual presentation tools, automation and efficiency tools (AI), and statistical analysis software are a plus.
  • Understanding of clinical trials landscape and pharmaceutical drug development lifecycle.
Benefits
  • Competitive salaries
  • Annual performance-based bonuses
  • An equity-based incentive program
  • Generous vacation
  • Paid wellness days
  • Support for learning and development
Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills & Tools
medical writingscientific publicationsliterature reviewsclinical trialshealth economics outcomesreal world evidence researchmedical editingquality reviewdata interpretationstatistical analysis
Soft Skills
collaborationcommunicationcritical readingorganizational skillsleadershipattention to detailinterpersonal skillsproject managementadaptabilityproblem-solving