Head of Medical Writing Expert
vor 3 Wochen
Key Responsibilities:
Establish and maintain medical and regulatory writing best practices to ensure consistency and quality of documents.
Lead a team of medical writers to generate key documents in internal clinical partnerships and support key documents in Artivion partnerships.
Strategically complete key documents such as clinical study protocols, clinical study reports, and regulatory submissions.
Coordinate document writing, review, and revision to ensure high-quality documents in conformity with program strategy and objectives.
Requirements:
Medical degree or natural science degree.
Long-standing experience as a medical writer in the medical/biomedical industry with increasing responsibility and technical development.
Proficient in writing protocols, manuscripts, and study reports.
Aptitude for compilation, analysis, and presentation of data.
Ability to communicate fluently and effectively in writing and verbally.
What We Offer:
An exciting field of activity in a challenging clinical environment.
An autonomous area of responsibility.
Active participation in an international clinical team.
Intensive training with a mentoring program.
Diverse benefits such as mobile working, bike leasing, and company pension.
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