Publications Scientific Communications Associate
We are seeking a highly skilled Publications Scientific Communications Associate to join our Global Scientific Communications team.
The successful candidate will work collaboratively with cross-functional teams to develop and prepare scientific publications, including abstracts, posters, manuscripts, and presentations, as well as regulatory documents such as protocols, clinical study reports, briefing documents, regulatory responses, and marketing authorization applications.
Key Responsibilities:
* Document Preparation and Development: Prepare, develop, and finalize documents, including abstracts, posters, manuscripts, and presentations, as well as regulatory documents.
* Data Collection and Evaluation: Collect and evaluate data, information, and input from multiple sources, functions, and regions.
* Publishing and Regulatory Documents: Plan, write, edit, review, and coordinate the publication of scientific data in peer-reviewed journals and forums, and/or regulatory documents supporting clinical development/product registration.
* Document Initiation and Coordination: Conduct effective document initiation to ensure authoring team alignment and understanding.
* Scientific Narrative and Argumentation: Build persuasive and scientific-based arguments that support the purpose of complex and strategic documents.
* Quality Checks and Document Finalization: Ensure quality checks for accuracy, collate reviewer's comments, adjust content of document as required, and prepare final version.
* Flexibility and Teamwork: Exhibit flexibility in moving across development and preparation of multiple document types, and work with teams to ensure smooth and timely development of documents.
* Timeline Management and Issue Escalation: Influence or negotiate change of timelines and content with other team members, and escalate issues, as appropriate, to ensure document completion.
* Authorship Criteria and External Partnerships: Advocate internally and externally for appropriate authorship criteria on all applicable work products, and build and manage relationships with vendors/alliance partners.
* Oversight and Quality Assurance: Provide oversight on individual deliverables, including timeline management, delivery of feedback, and issue management, and participate in in-licensing and co-development activities.
Requirements:
* Education: Bachelor's degree in scientific, health, communications, or technology-related field, or Bachelor's degree in any field with at least two years of clinical development experience.
* Language Skills: Demonstrated experience of verbal and written English skills in the medical, scientific, or technical writing field.