Description
The role manages clinical trial contract and confidentiality agreements, including initiating site contact, preparing and revising CDA and CTA language, coordinating legal counsel, tracking execution and status, maintaining files and archives, and processing consultant paperwork. It requires strong organization, confidentiality, communication, information-technology skills, and at least two years of professional administrative or business experience, along with pharmaceutical or clinical research organization experience and knowledge of FDA, ICH, and GCP requirements.
