Our client is looking for an experience Global Clinical Trial Manager who can help support their late phase (II/III) study initiatives. This person will need to be extremely hands on and dive into the projects they have that need support. They need someone who can be the primary communicator between the vendors (in total they have 12 vendors, but 1 large vendor who requires the most communication) to help relay between the two parties what needs to be completed. This person will be required to keep track of those studies and they would like this person to have experience with CAPA’s and be able to identify issues with the IT system, what issues need to be escalated, work closely with the leads for follow through, overview of the study management teams, and collaborate cross functionally. They are primarily nephrology so that is preferred but will accept any therapeutic area (majority of the company came from oncology to begin with.) They would love if someone had a deep understanding and knowledge of Labs and Lab Testing (urine tests, PK sampling, sampling management.) Global Trial experience is a must, but if this person has Import/Export licensing that would be a huge plus for them. This individual can come from a CRO or end sponsor background, as long as they are hands on and willing to dive deep into the root causes of standing issues for the studies.
Global Clinical Trial Management, Vendor Management/Oversight, Study Management/Oversight, Late Phase (II/III), CAPA
Kidney/Nephrology, PMP certified, Import/Export Licensing, Lab experience (for sampling purposes)
Remote: Clinical Trial Manager (232215)