Supports Clinical Research Associates (CRAs) to manage specific activities related to clinical projects.
Requirements
Requires a Bachelor’s degree in related field
High level of personal and professional integrity and trustworthiness with strong work ethic and the ability to work independently.
Good computer skills in usage of MS Office Suite
Strict attention to detail
Good written and verbal communication skills
Must be able to work in a team environment
Adhere to all company rules and requirements
Responsibilities
Participate in site start-up, maintenance, and close-out activities (e.g. tracking site progress, creating regulatory and subject binders, investigate discrepancies, etc.)
Provides support to CRAs who are conducting site visits, as needed.
Serves as quality control for study-related documents and is accountable for content accuracy to ensure compliance with GDP, US and OUS regulations, and internal company procedures
Maintains organization, preparation and ordering of supplies required for clinical studies.
Provides support to CRAs for preparing documentation, reports, and presentations.