Job Title:  Clinical Scientist Position Responsibilities Responsible for participating in the operational activities involved in the planning, conduct, and completion of clinical trials (activities include ordering clinical supplies, collection review and filing of clinical trial and regulatory documentation, preparation of monitoring guidelines, correspondence with investigative sites on routine matters concerning on-going clinical trials, etc) Participate in protocol and CRF development  Participate in the development of INDs, IND Annual Reports, IDBs, clinical study report, etc. Implements and continually reviews tracking procedures to ensure assigned projects which are not proceeding as anticipated are immediately and effectively reevaluated Maintains an active liaison with members of other groups involved in the drug development process, particularly Data Management, DRA, Drug Safety, Pharmaceutics and the CRA group. Participates in Clinical Project Team meetings.  Performs in-house review of selected clinical trial data. Ensures data discrepancies are resolved. Uses independent action and judgment during the data cleanup process except where such judgment requires medical judgment  Adheres to governmental regulations and company SOP’s when executing assignments Position Requirements College Degree and 4-6 years experience in clinical research or an advanced degree in appropriate science field with 3 years experience in clinical research. Benefits Blue Cross/Blue Shield Medical and Vision Dental Insurance 401K Plan with Company Match Holiday and Vacation Pay Relocation Assistance