Regulatory Gap Assessment of a Protocol
Our client will run a small safety study for 48 participants but need their brief protocol reviewed and potentially drafted.
Our client will run a small safety study for 48 participants but need their brief protocol reviewed and potentially drafted.
Creation of and virtual delivery of a PowerPoint E6 R3 training for various departments such as regulatory affairs, clinical monitoring,
Advarra is seeking a part-time IRB Manager. This position can be remote or onsite. The IRB Manager will be responsible
Advarra is seeking a part-time Clinical Research Coordinator to work onsite in Rochester, New York. This part-time opportunity is 20
Advarra is seeking a full-time Research Manager to work onsite in Rochester, New York. This position is ideally onsite but
Advarra is seeking a full-time Research Operations Manager to work onsite in Hartford, Connecticut. Oncology experience is highly desirable. The
Advarra is seeking a full-time Clinical Research Coordinator to work onsite in Hartford, Connecticut. Oncology experience is required. The Clinical
Advarra is seeking a part-time and full-time Clinical Research Coordinator to work onsite in the Cambridge/Boston, MA area. The Clinical
Advarra is seeking Clinical Research Coordinators to join our talent pool for future opportunities. The Clinical Research Coordinators will plan, direct, and