12 ago
|
Bristol-Myers Squibb
|
Bogotá
12 ago
Bristol-Myers Squibb
Bogotá
Bristol Myers Squibb in Bogotá seeks a Scientific Writer II (Manager level) to coordinate and author regulatory documents, ensuring scientific, medical, and regulatory inputs are integrated across cross-functional teams. You will leverage AI-assisted tools to enhance efficiency and maintain prototypes and shells for timely submissions.
The role requires 2–4 years in regulatory documentation, strong writing ability, and understanding of general drug development, with hybrid work arrangements in
📌 Senior Regulatory Writer – Clinical Documents Lead (Bogotá)
🏢 Bristol-Myers Squibb
📍 Bogotá