Preclinical Medical Writer

전망: 209

갱신일: 26-03-2024

위치: Basel Basel-Stadt BS

범주: 마케팅 / 홍보 인쇄

산업: Staffing Recruiting Biotechnology Pharmaceuticals

수평: Entry level

직업 종류: Full-time

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작업 내용

For one of our pharma client in Basel Land area, we are looking for a

Preclinical Medical Writer

General Information

Tasks And Responsibilities

Serve on early development and life cycle teams as the preclinical medical writer to support the development of individual compounds in a wide range of therapeutic areas
Compile, edit, and manage the review of preclinical sections of regulatory documents (IBs, briefing books, IND/NDA/MAA Modules 2.4, 2.6, 4) authored by cross-functional teams
Perform quality control checks of the above documents to ensure accuracy, completeness, and scientific robustness of content, consistency of reported preclinical data, compliance with Idorsia style guides etc.
Review, edit, and archive nonclinical study reports using an electronic document system
Support preparation and submission of preclinical publications

Must Haves

Masters or PhD (highly preferred) degree in life sciences
Excellent written and spoken English including scientific terminology
At least 1 year of experience as a medical writer or in a similar role (scientific editor, regulatory specialist)
Ability to make own judgment about the robustness of a scientific statement and whether it is supported by the available data
Ability to effectively communicate with other members of a cross-functional team (e.g., preclinical and clinical researchers, regulatory specialists, project managers) on a daily basis
Ability to prioritize tasks while working on multiple projects in parallel
Sharp eye for detail
Advanced knowledge of Microsoft Word (styles, cross-links, bookmarks, tracked changes, etc.)

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