• Will help with Day to day activities with PMs
• Ideally looking for someone with image management experience
• Breast and skeletal health product lines – imaging modalities – when doing research have lots of images that come in house – tracking and logging images or sending in batches to other team members. Able to be trained but helpful if they have that experience
• Hybrid – 2-3 days in office
• Internal lab – if activities in the lab, would ask for this person to be onsite to work on activities in the lab.
• BG in research is great

 

Assist with preparation, planning, execution and close-out of clinical trials
- Serve as document control coordinator and assist with maintenance of the Trial Master File
- Assist with site feasibility collection and data entry
- Assist with project and site level set up in the Clinical Trial Management System
- Create Investigator Site Binders
- Assist with IRB submissions and annual review as needed
- Assist CRA with collection and or review of essential documents as needed
- Maintain spreadsheets to support study progress including files and logs
- Assist with ordering clinical supplies
- Facilitate and or track site shipments and assist with shipment handling and management
- Participate in team meetings and generates meeting minutes
- Provide Monitor Listings to external vendors and or sites as requested
- Perform quality control functions on clinical trial documents
- Assist CRA with monitoring visit activities as needed