BeOne is seeking a Senior Clinical Research Associate to join their team. The successful candidate will be responsible for executing clinical monitoring activities, monitoring clinical trials, and collaborating with Country and Regional Clinical Study Teams.
Requirements
- Complete appropriate therapeutic, protocol and clinical research training/CRA training
- Perform site selection and evaluation
- Provide protocol and related study training to assigned sites
- Conduct onsite/remote pre-study, initiation, routine monitoring and closeout visits
- Manage sites and site performance
- Ensure copies/originals site documents are available for filing in the Trial Master File (TMF)
- Establish regular lines of communication with sites and reports site progress, issues and proposed action to Clinical Operations
- Collaborate with Country and Regional Clinical Study Managers and clinical study sites
- Evaluate the quality and integrity of site practices – escalating quality and/or GCP issues
- Mentor junior staff (Associate CRA and CRA)
Benefits
- Generous Paid Time Off
- 401k Matching
- Health Insurance
- Paid Vacation
- Relocation Assistance