Job Description:
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 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. They would love if someone had a deep understanding and knowledge of Labs and Lab Testing. 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.
Job Requirements:
Start Date: ASAP
Duration: 1 Year
Hours: 40 hours (would be open to someone part time 20+ hours)
Skills: Global Clinical Trial Management, Vendor Management/Oversight, Study Management/Oversight, Late Phase (II/III), CAPA
Plus: Kidney/Nephrology, PMP certified, Import/Export Licensing, Lab experience (for sampling purposes)
Remote: Global Clinical Trial Manager (232077)
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