Sr Clinical Research Associate (CRA)

Let’s talk about some of the key responsibilities of the role: As an investigator site facing role, the Sr. CRA will act as a customer advocate through a study life cycle. Understand and support study goals in alignment with corporate goals. Organize and maintain clinical study documentation (e.g., Trial Master Study Files) including preparation for internal/external audits, final reconciliation and archival. Where appropriate, responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits and appropriate documentation (confirmation, follow-up letters, communication logs, as required).…