המקום בו המומחים והחברות הטובות ביותר נפגשים
Preparation of Clinical Documents: Write and edit high quality clinical documents, including clinical protocols, study reports, regulatory submission sections, and investigator brochures. Co-ordinate review and approval of documents following SOPs and external guidelines (e.g. ICH-E3 for clinical study reports). Provide support to other departments (e.g., nonclinical).
Maintain Document Standardization: Use templates to ensure quality and consistency. Perform scientific review and quality checks of others’ documents to ensure compliance with document standards and guidelines.
Use of Document Management Systems: Import documents into the document management system and co-ordinate creation of published outputs.
Update SOPs and Model Documents: Review and update Medical Writing SOPs and model documents in line with latest guidelines.
Ensure Quality Compliance: Follow quality manuals and policies, complete compliance training, and report any quality issues.
Educational Background: Degree, MSc, or PhD in a scientific or medical field.
Experience: Demonstrated experiencein medical writing in industry, with proven ability to produce clinical protocols and reports independently and a knowledge of ICH and health authority guidelines.
Skills: Excellent communication and time management, proficiency in MS Office, and experience with electronic document management systems.
Self-Motivated: Able to work independently and co-ordinate workload across a number of projects to meet deadlines.
Detail-Oriented: Maintain high standards of quality and consistency. Excellent proof reading skills.
Problem-Solver: Identify and address process and product quality gaps.
Team Player: Provide support to other medical writers and other functions and participate in continuous improvement.
Technical Knowledge: Proficiency in MS Office and familiarity with Document Management Systems
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