Responsibilities
- Overseeing initiation activities for proposed clinical trials and entering them into the organization's research program system
- Building and maintaining collaborative relationships across internal departments, research sites, physicians, contract research organizations, and pharmaceutical partners
- Acting as the main point of contact during the feasibility, planning, and implementation phases of clinical trials prior to site activation
- Establishing and nurturing partnerships with pharmaceutical sponsors and CROs offering potential research opportunities
- Keeping an updated database of prospective pharmaceutical and CRO collaborations
- Promoting research capabilities and services to pharmaceutical companies, CROs, and industry contacts
- Strengthening industry connections through professional networks and online platforms to identify new study opportunities
- Delivering updates and relevant information about ongoing study start-up efforts during sponsor meetings
- Monitoring and recording site-specific metrics related to the clinical trial activation timeline
- Completing additional tasks as needed
Work Arrangement
Remote (Country)
Other
- This is a remote position based in the US
- Relocation assistance and visa sponsorship are not available for this position
- Occasional travel required
Not available
