Summary of Role: To ensure that Investigators are conducting clinical trials in accordance with international Regulatory and Ethical guidelines for Good Clinical Practices (GCP) and International Conference on Harmonization (ICH). May be responsible for assisting the RA Department in the preparation, compilation, submission and maintenance of regulatory documentation required by international regulatory agencies for clinical trials and marketing applications. This is a full-time, direct hire opportunity for an experienced CRA/SCRA residing in the US. Ideal candidates should have a variety of trial monitoring (field & remote) and full site management experience working with Cell & Gene Therapy trials and/or Oncology trials. Location needs for Oncology are W