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Responsible for the management of assigned clinical trial(s) and the physician training events by leading cross functional teams that may include tasks specific to study start up, regulatory, contract and budgeting, safety, medical monitoring, training event planning, etc. Serves as the clinical trial/project point of contact and the liaison with the CRO, third party vend
Posted 1 day ago
Review SOWs and other related contracts to identify, evaluate and negotiate with third party providers, to secure cost effective services and mitigate risk. Create/ Review/ Validate Analytics such as spend reports, savings, and contracts. Analyze market trends, pricing, and industry developments to inform Strategic Sourcing decisions. Lead RFP/RFI of supplier negotiations
Posted 1 day ago
OVERVIEW We are currently searching for a skilled professional to join a well known client's team as a Process Technician in Exton, PA. Under supervision and guidance, the Process Technician of Upstream Operations will be responsible for hand on executing the routine operation, maintenance, and periodically requalification of cell culture based upstream production equipmen
Posted 5 days ago
OVERVIEW We are currently searching for a skilled professional to join a well known client's team as an Administrative Coordinator in Exton, PA. Their work will have a direct impact on the organization and the larger clinical industry, making this an amazing career opportunity. RESPONSIBILITIES The Administrative Coordinator will prioritize workload and deliver specific cl
Posted 5 days ago
OVERVIEW We are currently searching for a skilled professional to join a well known client's team in the role of Sample Management Lab Project Manager. Your work will have a direct impact on the organization and the larger clinical industry, making this an amazing career opportunity. MAIN RESPONSIBILITIES AND ACCOUNTABILITIES Responsible for the planning, oversight of test
Posted 15 days ago
Develops scientific understanding of assigned program and protocol requirements Supports protocol design and development strategy for clinical trials Manages protocol development process; including writing support, reviewing, adjudication/resolution of cross functional comments, and ensuring high quality final document Contributes to the development of Informed Consent Fo
Posted 1 month ago
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