- 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
WhatYou'llBring:
- Paralegal certification or Associate’s degree
- At least two years of experience in a professional administrative/business role
- Fluent in spoken and written Italian and English