-Ability to coordinate new trials with Drug Sponsors, including Site Visits, IRB submission and re-approvals.
-Protocol Specific and Non Protocol Specific study trainings.
-Regulatory Binder organization including Study administration work, emails to and from sponsors, and updating trial binders.
-Ability to work in a fast paced trial setting, with multiple trials ongoing at one time.
-Ability to delegate staff and ensure proper protocol is being followed for each delegated task.
Past Drug Trial experience mandatory. Please provide references confirming past experience.
Job Types: Full-time, Part-time, Contract