Medical Writer jobs in Missouri

Veradigm Life Science

The Veradigm Network is well-positioned to address the unique needs of Life Sciences customers. By leveraging the Veradigm Network, research data and associated insights become both an output of care delivery, as well as additional knowledge to improve quality of care, a true virtuous cycle.

Our portfolio of solutions provides insights using real-world data directly sourced from the Veradigm Network. These solutions can help Life Sciences customers discover timely, actionable real-world evidence to improve patient experience and outcomes, and demonstrate how their products can benefit appropriate patient populations.

Job Summary

Veradigm Life Sciences is looking for a Medical Writer, Publications to complement its growing team of healthcare analysts, data scientists and researchers to collaborate on healthcare database analyses and product development. As a member of the RWE team, this Medical Writer will directly contribute to the generation of written deliverables produced by the team, including final reports, white papers, abstracts, posters, and manuscripts.

The Medical Writer, Publications collaborates with members of cross-functional teams to prepare and disseminate high quality written deliverables that communicate complex ideas, methodologies, and results to clients and other stakeholders.

What you will contribute:

• Prepares, edits, and finalizes study protocols, final reports, white papers, conference abstracts and posters, manuscripts, and other scientific written deliverables as needed

• Participates in deliverable-related scientific communication planning meetings with clients

• Collaborates with internal and external stakeholders to interpret study results and ensure results and statistical interpretations are accurately and clearly reflected in the deliverable

• Conducts scientific literature reviews

• Coordinates the internal and external document review process ensuring conflicting and/or ambiguous comments are clarified and appropriately addressed

• Ensures documents are generated in accordance with agreed internal processes and standards, are submission ready, and are appropriately stored in agreed document management system

• Performs quality assurance on medical writing deliverables prepared by other authors

• Maintains the publications database

The ideal candidate will have:

Education

Masters or PhD degree in a relevant field of study (health sciences, health economics, public health, epidemiology, or other quantitative discipline)

Experience:

• A successful applicant should have 1-3 years of writing experience in pharma/biotech/medical communications or related field OR a strong publication record as first author of research presented at professional congresses and peer-reviewed journals.

• Outstanding writing, editing and communication skills and excellent command of the English language

• Exceptional attention to detail: style/consistency, good grammar, scientific accuracy, and experience in QCing work and sign-off of printer proofs

• Excellent time management skills for managing multiple individual and team tasks simultaneously while completing work within allocated time frames

• Highly proficient with word processing (Word), spreadsheets (Excel), presentation programs (Power Point), scientific search engines (PubMed, Google Scholar), and online journal/conference submission systems

• Familiarity with reference software and graphics design software preferred

• Applicants should be ready to work in a highly collaborative environment and have a great attitude (e.g., team-focused, loves to get things done).

Travel Requirements:

No usual travel.

Working Arrangements:

Work can be performed in a standard office environment or in a home office setting.

Compliance

Job responsibilities include fostering the Company's compliance with all applicable laws and regulations, adherence to the Code of Conduct and Compliance Program requirements, policies and procedures. Compliance is everyone's responsibility.

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