Clinical Documentation Coordinator
We are looking for experienced Clinical Documentation Coordinators to help us organize a client's Trial Master File for a large project. As part of the project, you will be responsible for performing Quality Control Reviews on individual documents, transmittal of files into the TMF or the Data Management System, population of CSR appendices, and generating various reports, among other tasks.
Excellent communication skills, attention to detail, and the ability to work with various software and computer tools are all critical components of this job. You will be supporting the clinical operations and document management teams, so interpersonal skills and the ability to work well within a team are also essential.
This is an exciting project in a quickly growing client with an excellent outlook. Interested candidates please respond to this posting with an updated CV. If you have not worked with BioBridges in the past, please be prepared to provide professional references.