12 ago
|
Bristol-Myers Squibb
|
Bogotá
12 ago
Bristol-Myers Squibb
Bogotá
Bristol Myers Squibb is seeking a Senior Scientific Writer I in Bogotá to coordinate and author regulatory documents for global submissions. The role requires leading cross-functional teams to ensure high-quality documents such as IBs, CSR, and CTD modules are produced on schedule.
The position emphasizes strong writing, data interpretation, and knowledge of integral drug development, with hybrid work options and engagement across cross-disciplinary functions to support lifecycle management of
📌 Senior Scientific Writer | Regulatory Documentation Lead (Bogotá)
🏢 Bristol-Myers Squibb
📍 Bogotá