Job Overview: In the role of In-House Clinical Research Associate, you will be working in a global clinical research organization that is dedicated to advancing the development of new medicines and biologic therapies for challenging diseases. Your key responsibility will be to ensure that patients' rights and safety are protected and that clinical trials are conducted per regulations and the protocol. Key Responsibilities: - Ensure accurate tracking of investigator recruitment activities using the Clinical Trial Management System (CTMS) - Perform essential document collection, review, maintenance, and close-out activities - Support investigators and investigative staff in fulfilling obligations regarding local submissions according to regulatory requirements Requirements: - Experience with PC-Windows, word processing, and electronic spreadsheets required - Knowledge of local regulatory authority drug research and development regulations required - Clinical trials support or pharmaceutical industry experience required