The client is currently in need of helping the medical writing team on an oncology program Currently they are in search of someone who comes from a clinical scientist background who has experience with global clinical oncology development. Consultant also needs to have deep understanding of clinical data review monitoring. This person must also have Clinical Research experience. Examples of documents this consultant will be working on are CSR, Protocols, IB’ s, etc.
Day to Day Responsibilities:
This consultant must come with a firm GCP and scientific background specific to oncology. The client currently does not have enough man power to complete all the documents that need to be written. The types of documents that this consultant will be working on will be focused in the scientific world. Anyone applying for this role must have subject matter expertise on how to properly write CSR’ s, Protocols, and IB’ s in accordance to GCP guidelines. The client is a pharmaceutical company therefore pharmaceutical expertise is a necessity.
Job Type: Contract