4. 0 Full-time 15 hours ago Full Job Description Position Highlights: Working in a team-oriented environment with intelligent and highly motivated clinician researchers and research operations team Working in an innovative, newly formed office at Moffitt called the Non-Therapeutic Research Office (NTRO), with the opportunity to provide feedback to how the office is shaped for the long term This department recognizes work life balance. . Although this is an in-person position, we support flexibility for quiet days from home once trained. The NTRO office provides education routinely on research topics, in addition to the initial training period. . We want this opportunity to be one that allows the staff member to continually grow and learn relevant topics for the role. The Ideal Candidate: Detail oriented Experience in developing and working with databases and reporting including human subject databases and/or biorepository data Experience in GI oncology An independent individual that has experience in the wet lab, in addition to non-therapeutic research experience Demonstrated experience in coordinating multiple studies with high quality, compliance and independent work in outpatient clinics. . Preferred hands-on research experience, knowledge of research process and/or research procedures including research regulations. A go-getter personality that can approach patients with ease. . Someone who enjoys a fast-paced clinical environment and would like to create a career in research or a future career in medicine An individual that likes to learn and has a can-do attitude Excellent communication and critical thinking skills Team player attitude, and enjoys contributing to the larger picture An individual that would like to build their career at Moffitt and in research. Career pathways are being built for retention and growth Someone who has been trained in phlebotomy or would like to be trained once hired Responsibilities: Responsible to provide research coordination support for PI initiated research studies using the biobanking protocol and study specific protocols through all stages of the assigned studies ranging in complexity and has primary responsibility for non-clinic facing study coordination activities. . Responsible for performing data management and documentation activities including building database forms, maintaining research databases using internal and external systems and keeping accurate and compliant study records. Working independently, under the guidance of the PI and the NTRO Supervisor, the Research Services Project Coordinator is directly responsible to perform research coordination activities for non-therapeutic studies conducted in the Moffitt Cancer Center clinics. . The position will contribute to the development and execution of department level and PI initiated research studies conducted using the biobanking protocol or study specific protocols, developing data recording methods for assigned studies, and performing study coordination for studies ranging in complexity. Credentials and Qualifications: Bachelor’s degree in biological science, public health, behavioral research or related field with minimum of 3 years of experience in clinical research, research or related field OR Master’s degree with 1 year of relevant experience required. . Experience in developing and working on databases and reporting including human subject databases and/or biorepository. Experience in coordinating multiple studies with high quality compliance and independent work in outpatient clinics. . Proficient in educating teams, training, mentoring, presenting study progress and study coordination results independently. Location: H. . Lee Moffitt Cancer Center & Research Institute NTR Clinical Rsch Oper Schedule: Full Time, Day Shift, M-F 8-4: 30.