Roche is seeking a Clinical Development Lead (Medical & Scientific Writing) to partner with the CEI team and drive clinical evidence generation for cutting-edge IVD programs. You will own end-to-end documentation strategy and lifecycle management for regulatory submissions.
You will design protocols, author CSRs and IVDR documents, review literature, mentor junior staff, and collaborate with Medical Affairs to produce manuscripts and posters. Flexible hybrid work in AZ/USA.
#J-18808-LjbffrIVD Clinical Development Lead - Regulatory Writing in tucson at Unknown Company
This position is listed as full time and hybrid.