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Senior Medical Content Specialist
2 tygodni temu
**Job Summary:**
We are seeking a highly skilled Senior Medical Writer to join our team. The ideal candidate will have a strong background in medical writing, with experience in developing high-quality content for clinical trials and regulatory documents.
The Senior Medical Writer will work independently or as part of a team to develop clinical documents, including protocols, study reports, and investigator brochures. They will also be responsible for ensuring the consistency and quality of all documents issued.
The successful candidate will have excellent English language skills, both verbal and written, and will be able to communicate effectively with stakeholders at all levels.
- Develops high-quality clinical documents, including protocols, study reports, and investigator brochures
- Ensures the consistency and quality of all documents issued
- Communicates effectively with stakeholders at all levels
- Maintains accurate records of document development and revisions
**Requirements:
- PhD or equivalent expertise
- Up to 5 years' clinical regulatory writing experience in the pharmaceutical industry
- A good understanding of basic drug development
- Knowledge of scientific methodology and statistical principles in the design, conduct, and description of clinical research
- Understanding of how to interpret, describe, and document clinical data
- Working knowledge of International Committee for Harmonisation (ICH) / Good Clinical Practice (GCP)
- Strong IT skills
- Excellent English language skills (verbal and written)
What We Offer:
- Career opportunities in a global healthcare company
- Contract of employment
- Attractive reward package
- Hybrid working model
- Extensive support of work-life balance
- Life insurance and pension plan
- Private medical package
- Sports cards
- Possibilities of development within the role and company's structure
- Personalized learning approach