Senior Specialist, Medical Communications, Scientific Publications

This is a fully remote position, open to applicants in United States.

📋 Description

• Assisting in the implementation of the scientific publications and communications strategy.

• Creating medical writing and communications materials, including slide presentations and scientific papers.

• Conducting literature reviews and background research; formulating outlines and multiple drafts; gathering, organizing, and integrating feedback from authors and reviewers.

• Collaborating with various internal teams (such as Clinical Science, Clinical Operations, Product Portfolio/Global Commercial, Research & Innovation, Marketing, Market Access, Intellectual Property, Medical Information, and Pharmacovigilance Teams) to achieve corporate goals throughout the organization.

⛳️ Requirements

• An advanced degree in a scientific field with relevant experience: a Master’s degree with 4+ years or a PhD (preferred) with 2+ years of applicable experience is required.

• At least 5 years of experience in publications (including peer-reviewed manuscripts, abstracts, and related poster/oral presentations). Experience in the industry and/or pharmaceutical sector is necessary.

• A minimum of 2 years of experience in Oncology, health economic outcomes research, and/or real-world evidence research is advantageous.

• Required experience in medical editing and quality review of scientific publications (e.g., regulatory documents, manuscripts, abstracts, etc.).

• Familiarity with the current publication environment and pertinent standards/documents (e.g., ICMJE Authorship Guidelines, Good Publication Practice guidelines, AMA Manual of Style, EQUATOR reporting guidelines).

• Proficiency in critically reading, interpreting, and conveying information from scientific literature, including peer-reviewed manuscripts and regulatory documents (e.g., protocol, investigator's brochure, clinical study report).

• Highly proficient in Microsoft PowerPoint, Word, Excel, and reference management software. Experience with EndNote, visual presentation tools, automation and efficiency tools (AI), and statistical analysis software is a plus.

• Knowledge of the clinical trials landscape and the pharmaceutical drug development lifecycle.

🏝️ Benefits

• Competitive salaries.

• Annual performance-based bonuses.

• Equity-based incentive program.

• Generous vacation policy.

• Paid wellness days.

• Support for learning and development.