Takeda is seeking a Senior Manager, Clinical Trial Delivery and Pharmacovigilance Documentation Excellence in a hybrid role in Cambridge, MA. You will oversee TMF and PV documentation across the portfolio, act as SME, and partner with Clinical Trial Delivery, Medical, PV, and QA.
The ideal candidate has 6+ years in pharma/biotech/CRO with TMF/eTMF, regulatory knowledge (ICH E6, 21 CFR Part 11, EU CTR), strong governance and vendor management, and a track record of process improvements and
#J-18808-LjbffrSenior Manager, Trial Delivery & PV Documentation in kendall square at Unknown Company
This position is listed as full time and hybrid.