YES Group LLC
We are looking for a Manager Regulatory Affairs to be based in the Philadelphia, PA area. The Manager Regulatory Affairs provides project management and regulatory expertise to clients developing prescription pharmaceuticals to assure their...
Bulletproof Documentation, Inc.
WE ARE STILL HIRING! SENIOR TECHNICAL WRITERS: Biologics GMP Manufacturing: Contract positions
Projects include technical transfers, preapproval inspection readiness, document re-engineering!
•Create (from-scratch) and/or...
Serve as the Medical Monitor for ImaginAb clinical trials serving as the primary Medical Monitor responsible for monitoring the safety of enrolled subjects on assigned trials.
Consultant fee $250/hour.
Length of the contract: 18-24 months.
Position Purpose: The purpose of this position is to be the leader of the Bio Analytics strategy for the NGIG project. All development and QC analytics would be under this positions direct accountability.
Major Tasks: The major tasks of this role...