Clinical Data Programmer II

The CDP-II shall be responsible for designing, programming, testing and maintenance of clinical trial databases in different clinical trial applications in accordance with standards. Perform external data loads, i.e. labs, ECGs etc., as needed. Act as liaison with vendors to establish data transfer specifications standards. Ensure all programming activities and processes performed are conducted in accordance with standard operating procedures and good programming practices. Knowledge in developing, validating and maintaining clinical trials built in different EDC applications Ability to learn new process, programming languages and adapt with new technologies