CRF Development


Clinical Trial Material Management


Project Management accountable to ensure all relevant studies for one of the largest pharmaceutical companies in the US. Assist with maintaining relationships and monitor performance of CRO’s and other vendors. Collaborate with Clinical Operations functional groups (US Monitoring, Data Management, and Operations Management) to ensure on time delivery of studies. Provide input into identifying implications of study progress upon overall timeline goals conduct plans. Manage study start-up, conduct and close-out. Manage clinical trial material. Management of CRO’s or other outsourcing partners as appropriate. Provide input into content and execution of investigator meetings / may present selected topics. Provide input into development of CRF and site selection.