Description:
R&D Coauthoring Consultant Work location: Philadelphia, Pennsylvania (Onsite only) Required skills: R&D coauthoring consultant with demonstrating experience and mastering of Pharma process for regulatory submissions across R&D - research, development, safety, regulatory and medical. Ideal candidate would have prior consulting experience with planning, authoring, reviewing and approving regulatory documents including creation, version control, approval, and real-time co-authoring of all submis
Mar 17, 2025;
from:
dice.com