Site Contract Specialist

What You'll Do: Initiate site contact and follow-up as necessary to turn study confidentiality agreements (CDA) and study clinical trial agreement (CTA) drafts Administer contract language to ensure it remains within approved sponsor guidelines and work with legal counsel on contract revision and negotiation Facilitate CDA and CTA completion and execution Attend internal and external project team meetings and report on CDA and CTA progress Maintain contract files and internal/external CDA and CTA tracking sheets Update CTA status within the internal study start-up module for all assigned studies Assist with contract preparation, review, revision, execution and filing Advise appropriate parties of significant terms (e.g. expiration dates, renewal terms, compliance obligations, etc.) Assist with CDA preparation, review, negotiation, execution and filing. Maintain CDA tracking Maintain CDA archives Process new consultant paperwork and maintain files What You'll Bring: Paralegal certification or Associate’s degree At least two years of experience in a professional administrative/business role Experience working in or with a pharmaceutical company or a Clinical Research Organization (CRO) (preferred) Basic knowledge of medical and pharmaceutical terminology (preferred) About CTI CTI Clinical Trial and Consulting Services is a global, privately held, full-service clinical contract research organization (CRO) focused on the advancement of treatments for chronically and critically il