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Clinical Study Specialist (Hybrid)
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Warren, NJ; Armonk, NY; Cambridge, MA
About this role
Job title: Clinical Study Specialist (Hybrid)
What you will be doing
- Organizes and delivers analyzable reports and metrics to the clinical study lead
- Schedules and coordinates meetings, prepares agendas, presentation materials and minutes for clinical study team meetings and other study related meetings
- Collates data for assessments such as feasibility and site selection and reviews site usability database
- Contributes to review of study documents such as informed consent forms, case report forms and facilitates study document reviews per company standard operating procedures
- Compiles study manuals including but not limited to: study reference binders and manuals and maintains versioning of study reference materials (e.g., regulatory, pharmacy, and laboratory binders)
- Collates materials for training and investigator meetings
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