Scientific Writer Publications
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* As a Scientific Writer Publications, you will work with cross-functional teams to prepare scientific publications and regulatory documents.
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Responsibilities:
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1. Document preparation, development, and finalization, including planning, writing, editing, and reviewing.
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2. Collecting and evaluating data, information, and input from multiple sources, functions, and regions.
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3. Preparing scientific data for publication in peer-reviewed journals and forums, and coordinating the publication process.
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4. Conducting document initiation to ensure authoring team alignment and understanding.
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5. Assisting in building persuasive arguments that support complex documents.
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6. Ensuring key data is presented clearly, accurately, and concisely.
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7. Collaborating with teams to ensure smooth and timely document development and escalation of issues as necessary.
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8. Influencing or negotiating changes in timelines and content with other team members.
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9. Advocating for appropriate authorship criteria on all applicable work products.
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10. Working with internal and external speakers to develop and prepare presentations.
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11. Building and managing relationships with vendors and alliance partners.
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12. Providing oversight on individual deliverables, including timeline management, delivery of feedback, and issue management.
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13. Participating in in-licensing and co-development activities, ensuring the quality of data in documents.
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14. Supporting the implementation of outsourcing strategies by partnering with staff, management teams, outsourcing teams, technical lead consultants, and vendor staff.
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Requirements:
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* Bachelor's degree in a scientific, health, communications, or technology-related field, or equivalent experience in clinical development.
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* Demonstrated experience with verbal and written English skills in medical, scientific, or technical writing fields.
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* Experience writing regulatory, clinical trial documents, and/or publications.
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* Experience in clinical development, clinical trial processes, or regulatory activities.
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* Clinical pharmacology, therapeutic area, or other medical and scientific specific knowledge and experience.
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* Demonstrated project management and time management skills.
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* High-level end-user computer skills, including word processing, tables, and graphics.
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