Research Protocol Associate - Cancer Center

Participates in components of the clinical trial development, implementation, maintenance, and completion process as directed. Responsibilities may include but are not limited to: assisting with protocol/clinical research development and maintenance including gathering regulatory documents, drafting the informed consent, developing clinical trial budgets, identifying/coordinating study logistics/approvals and protocol modifications. Must be able to work in a complex environment and exercise good judgment in ambiguous situations. Must possess excellent problem-solving skills, oral, written, communication and interpersonal skills, and be comfortable interacting with individuals at all levels internal and external to Mayo Clinic. Participates on projects as assigned. Ideal candidate will be detailed-orientated and work with a sense of purpose. Provides input to standard operating procedures and working instructions. This is a hybrid position and must be located within 100 miles of a Mayo Clinic campus or Mayo Clinic Health System campus for occasional on-site expectations based on business needs. On-site expectations will be discussed during the interview process. A bachelor's degree is required OR associate degree or completion of college diploma program or certificate program with 2 years experience in the clinical research setting or related field. Must be proficient in the use of computers, Microsoft applications. Familiar with research systems, experience leveraging tools and technology. Prefer previous experience with reg docs, IRB submission, writing consent forms.