What will you be doing?
You will be accountable for the operational planning, feasibility, and execution of a clinical protocol. You may lead a team in key study planning, development and execution elements (e.
g., data management deliverables, protocol level plans / timelines, country / site selection, system updates, Investigator Meeting planning, communication plans, preparation of status update reports, study closeout activities).
You may serve as the clinical trial team (CTT) lead for timeline management, risk identification and mitigation, issue resolution.
You will be accountable for managing any study specific partners and / or vendors. You will also facilitate and collaborate with key internal / external stakeholders (study team, subsidiary country teams, vendors, committees, etc) in support of clinical study objectives.
What you need to have :
This is a home based position anywhere in the US or Canada