Science Writer
Company
Tempus AI
Location
Chicago, IL
Type
Full Time
Job Description
Passionate about precision medicine and advancing the healthcare industry?
Recent advancements in underlying technology have finally made it possible for AI to impact clinical care in a meaningful way. Tempus' proprietary platform connects an entire ecosystem of real-world evidence to deliver real-time, actionable insights to physicians, providing critical information about the right treatments for the right patients, at the right time.
We are seeking an independent and motivated Science Writer to join our Scientific Communications team to support cross-functional publication and internal R&D communication efforts. This individual is a clear communicator, effective collaborator, and proactive problem solver who works well with others. This individual will lead internal R&D and scientific communication initiatives that support information sharing and support publication activities (i.e., peer-reviewed manuscripts, conference abstract/presentation submissions). This individual will have the opportunity to work on a diverse set of projects across disease areas (e.g., oncology, cardiology, neurology, etc.) and collaborate with interdisciplinary teams of research scientists, medical professionals, medical science or scientific affairs liaisons, and/or commercial partners to communicate important research insights.
Responsibilities:
- Lead the preparation of scientific/clinical manuscripts for publication in top-tier peer-reviewed journals, including writing, editing, and proofreading drafts.
- Lead internal R&D communication initiatives (e.g. newsletter, confluence, department-wide quarterly all-hands).
- Collaborate on communication-related activities (e.g., support publication-related marketing materials) to enhance the visibility and impact of research publications.
- Draft, edit, and manage conference-related materials, such as abstracts, posters, and slide presentations.
- Effectively manage assigned publication roadmaps and review processes including timelines for document generation, submission, revision, and completion.
- Collaborate with authors to ensure they adhere to both external (Good Publication Practice [GPP], International Committee of Medical Journal Editors [ICMJE], and/or journal/conference-specific guidelines) and internal processes.
- Support publication-related data uploads into external repositories as needed and ensure compliance with internal data management standards.
- Perform literature/reference searches and support the generation of other technical documentation as needed.
Required Qualifications
- Advanced degree in biomedical/life sciences or quantitative field with relevant scientific/clinical background.
- Experience writing and submitting scientific manuscripts, abstracts, and other technical documents to conferences and journals, along with a track record of success.
- Exceptional scientific writing and editing skills.
- Ability to interpret, summarize, and translate primary scientific literature for a range of audiences.
- Intermediate or advanced knowledge in one of these areas: real-world data/evidence, human genomics, clinical research concepts, computational biology (machine learning, statistics, algorithms), and/or oncology.
- Familiarity with GPP and ICMJE guidelines.
Preferred Qualifications
- Experience with/knowledge of health economics and outcomes research (HEOR) and/or clinical development.
- Experience with Adobe Illustrator and Acrobat.
- Experience with/knowledge of genomic data types and archiving standards, as well as data and code reproducibility best practices.
- Experience working on and/or managing diverse research projects to completion.
- Experience with scientific/medical writing in an industry setting.
#LI-SH1#LI-Hybrid
We are an equal opportunity employer. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.
Date Posted
08/25/2024
Views
3
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