Contractor Freelance Medical Writer

Alphanumeric is seeking experienced Freelance Medical Writers based in Poland for project-based contract work.  

Advanced degree within life sciences and experience in medical communications writing is required.

Typical project-based work could include:

• Creating and editing PowerPoint presentations
• Scientific manuscripts
• Standard response letters
• Congress summary reports

Some client-facing work and travel are possible.

In this role, you will create original, high-quality, and scientifically accurate content in a myriad of standard medical communications deliverables.

All content will be developed to project specifications and timeline as outlined in a project brief.

This role interacts with Swiss life-sciences organizations, and requires experience working within that market.

Role Responsibilities:

• Collaborate with Alphanumeric team members and, at times, client leads to ensure projects are completed on time and within scope.
• Develop accurate and concise outlines, on-target first drafts, and proactively incorporate data/revisions as appropriate for high quality content development as needed for the assigned project.
• Prioritize scientific accuracy, clarity, and ethics when creating, referencing, reviewing, or editing content.
• Write materials with tone and language appropriate for the target audience and ensure an appropriate and effective story flow is in place.
• When incorporating edits and/or updates for external authors, ensure their voice is maintained within the piece.
• Provide appropriate, robust references and annotate documents as required for the content being developed.

Requirements:

• Minimum of 5 years of medical writing experience in a medical communications agency environment or in-house pharmaceutical company setting, or as a freelance writer; other types of relevant experience will be considered.
• Fluency in written German and English.
• Experience working with Swiss regulatory organizations.
• Being legally eligible to work as a freelancer in Poland.
• PharmD or PhD; other life science degrees considered with relevant experience.
• Proficiency with MS Office (specifically Word, PowerPoint, and Excel), the internet, and database searches (e.g., Pubmed, ClinicalTrials.gov).
• Attention to detail to manage documents throughout the review process and to ensure revisions and comments are addressed across consistently deliverables.
• Ability to interact in a professional manner with client leads.
• Has a working knowledge of standard compliance procedures and regulatory process and works diligently to ensure content produced adheres to Alphanumeric and client standards.

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