NTRO RESEARCH COORDINATOR II

at  H Lee Moffitt Cancer Center

Are you looking for an opportunity to be part of an innovative team and make an impact in the lives of those affected by cancer? As a member of the Moffitt Non-Therapeutic Research Office (NTRO) you may interact directly with community members and patients to enroll, educate, and guide participants through the experience of taking part in research. You may support non-therapeutic research in other ways including data entry, project and protocol management and quality assurance. Regardless, you will be a member of a collaborative team that ensures non-therapeutic research activities are moving forward safely, smoothly, and according to plan.
Our NTRO Research team comes from a variety of backgrounds and experiences, including public health, psychology, biological sciences and more. There are opportunities for those who have worked in other areas of public health as well as those who are looking for a new and exciting opportunity. Team members of NTRO work closely with community members, patients, patient families, study sponsors, and the clinical teams including physicians, pharmacists, nurses, and other health care providers.
These positions typically offer a Monday through Friday schedule, though some require occasional weekends. Most offer a hybrid schedule (mix of remote and on-site). Moffitt offers training and orientation. Relocation assistance may be provided.

POSITION SUMMARY:

The primary focus of this position is to coordinate one or more non-therapeutic research studies in multiple clinics at Moffitt. Coordination activities include participant recruitment and follow-up, specimen collection, data abstraction and entry. This position is expected to work under general supervision and direction from the Non-Therapeutic Research Office (NTRO) supervisor to implement and coordinate research, including administrative procedures.

CREDENTIALS AND QUALIFICATIONS:

• Associate’s degree in Public Health, Psychology, Biological Sciences or relevant field with two (2) years of relevant research experience required; OR Bachelor’s degree requires at least one (1) year of relevant research experience; OR Master’s degree no experience.
• Required knowledge of research protocols and/or study coordination.
• Required general knowledge of medical terminology, general commuter skills (Microsoft Office Suite).
• Preferred knowledge of EMR system (PowerChart) and clinical trial management systems (OnCore)
• Preferred experience entering data into electronic data capture systems (REDCap or similar)
  Moffitt Team Members are eligible for Medical, Dental, Vision, Paid Time Off, Retirement, Parental Leave and more. Tampa is a thriving metropolitan city, which has become a hub for ground-breaking research, welcoming individuals from around the globe. This diverse city is engulfed with rich culture, year-round activities, amazing cuisine and so much more. We strive for work/life balance.
  If you have the vision, passion, and dedication to contribute to our mission,
  then we have a place for you.
  Location: H. Lee Moffitt Cancer Center & Research Institute · NTR Clinical Rsch Oper
  Schedule: Full Time, Day Shift, 8:00-4:30 M-

• Screen, identify eligibility, and consent participants. This could be any research participant, including community based or clinically based participants depending on the study needs.
• Enters data and other pertinent information into the appropriate databases (i.e., REDCap, Power Chart, OnCore, sponsor specific Electronic Data Capture (EDC) system).
• Responsible for quality of the data coming in and ensuring that the protocol is being followed appropriately.
• Ensure proper specimen collection at the correct time points, in collaboration with Tissue Core and other stakeholders as appropriate.
• Updates protocols with PI’s guidance for submission to the Regulatory Specialist.
• Documents deviations timely and communicates with the proper stakeholders (PI, Regulatory, Management).
• Communication involves routinely conveying standardized information to the Regulatory Specialist of study needs; including amendments, new study submissions, and deviations.
• Communication involves routinely conveying standardized information with Tissue Core, PRISM, and other shared resources at Moffitt to ensure that the recruitment, data and specimen collection are being coordinated properly.