Proclinical seeks an Aggregate Reports Specialist for a contract role in Cambridge, MA with remote work options. You will manage aggregate safety reports and RMP activities across the product lifecycle, coordinating with GPSRM, CROs, and cross-functional teams to ensure timely safety outputs and regulatory compliance.
The role requires 3–5 years in pharma, PV system knowledge (Argus/Arisg), and strong analytical writing skills.
#J-18808-LjbffrRemote Aggregate Reports Specialist - Drug Safety in cambridge at Unknown Company
This position is listed as contract and able to be worked remotely.