Provides management and oversight of oncology clinical trials conducted at CalvertHealth.
Performs a variety of complex duties to support the conduct of clinical research, such as, facilitating the informed consent process, coordinating required research activities; collecting, compiling, and documenting clinical research data to ensure adherence to protocols and validation of information and documents.
Performs study specific regulatory processes in accordance with appropriate regulations, standard operating procedures and study specific protocols/plans.
Promotes the ethical conduct of research and ensures compliance with federal, state and institutional regulatory requirements.
Oversees the financial processes involved in a clinical program.
Coordinates pre-award and post-award activities to include assisting to create study budgets/Memorandum of Understanding, preparing Medicare Coverage Analysis and internal cost summaries, reconciling project budgets, facilitating sponsor invoicing, and coordinating site payments.