Independently negotiates initial or amended site Clinical Trial Agreements (CTAs) and budgets, and/or serves as escalation point and oversight for CROs negotiating site CTAs and budgets in support of assigned global Clinical Studies. Independently negotiates other initial or amended clinical Agreements such as Investigator Initiated Research Agreements (IIRs), Confidentia

OVERVIEW We are currently searching for a skilled professional to join a well known client's team as a Regulatory Specialist in Des Plaines, IL. The Regulatory Specialist role will have a direct impact on the organization and the larger clinical industry, making this an amazing career opportunity. RESPONSIBILITIES Responsible for implementing and maintaining the effectiven

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