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Clinical Editor
hace 2 meses
We are seeking a highly skilled Clinical Editor to join our FSP Medical Writing team at Thermo Fisher Scientific. As a Senior Document Review Specialist, you will play a critical role in ensuring the quality and accuracy of documents, including regulatory submissions, integrated clinical study reports, and publications.
Key Responsibilities- Review and edit documents to ensure they meet or exceed client expectations.
- Verify data in tables against source documents and ensure consistency with current regulatory standards and guidelines.
- Collaborate with authors to ensure compatibility with unique preferences and scientifically sound judgment.
- Maintain and communicate knowledge of current guidelines, templates, and industry standards.
- Coordinate the work of team members and track the status of documents being reviewed.
- Bachelor's degree or equivalent and relevant formal academic/vocational qualification.
- Previous experience in medical writing, regulatory affairs, or a related field.
- Thorough knowledge of medical terminology, statistical concepts, GCP, and regulatory requirements.
- Excellent analytical and communication skills.
- Ability to work independently and collaboratively in a cross-cultural environment.
Thermo Fisher Scientific offers a competitive remuneration package, annual incentive plan bonus, healthcare, and a range of employee benefits. We are committed to providing a dynamic and supportive work environment that fosters innovation, integrity, and involvement.
Our Mission is to enable our customers to make the world healthier, cleaner, and safer. We share a common set of values: Integrity, Intensity, Innovation, and Involvement, working together to accelerate research, resolve complex scientific challenges, drive technological innovation, and support patients in need.
