• Prepares, edits, and finalizes critical scientific materials for enhancing stakeholder resources across all of Lantheus’ pipeline and product portfolio including abstracts, presentations, manuscripts, white papers, review articles, and clinical case studies.
• Conduct periodic literature surveys and obtain relevant articles and references in support of writing requirements and responsibilities.
• Provide Medical Affairs support for the MLR (Medical, Legal, Regulatory) review process including serving as a backup reviewer for the (Senior) Director of Clinical Science Communications.
• Manage and coordinate work with external medical writing and publication vendors.
• Ensures that medical writing deliverables conform to International Committee of Medical Journal Editors (ICJME) and other relevant guidelines

 

Typical Minimum Skills and Experience and Education

BA/BS/MS/PhD Degree in a scientific discipline with 4-6 years of biopharmaceutical industry experience including 2 years of scientific writing with an emphasis on scientific abstracts, posters, oral (PowerPoint) presentations, and manuscripts. Experience with the oncology space especially in prostate cancer is preferred

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