NTRO RESEARCH COORDINATOR II

Moffitt Cancer Center; Tampa (FL); On-site; USD 32,000 - 48,000; Full time

Benefits offered by this job

Medical benefits

Dental benefits

Vision benefits

Paid time off

Retirement plan

Parental leave

Job summary

Moffitt Cancer Center in Tampa, FL seeks an NTRO Research Coordinator II to coordinate non-therapeutic studies under the PI's portfolio. You will screen participants, obtain consent, enter data into REDCap/OnCore, and ensure protocol compliance under supervision.

The role requires strong communication and problem-solving in a fast-paced environment. Ideal candidates have 1–2 years of research experience and familiarity with EMR systems and clinical trial management tools.

Qualifications

• Associate’s degree in Public Health, Psychology, Biological Sciences or relevant field with two years of relevant research experience.
• Bachelor’s degree requires at least one year of relevant research experience.
• Master’s degree with no experience.
• Required knowledge of research protocols and/or study coordination.
• Required general knowledge of medical terminology and Microsoft Office Suite.

Responsibilities

• Screen, identify eligibility, and consent participants.
• Enter data into databases such as REDCap, PowerChart, OnCore, or sponsor EDC systems.
• Responsible for quality of the data coming in and ensuring that the protocol is being followed appropriately.
• Ability to handle a higher volume of moderate complex studies.
• Communicate with Regulatory Specialist on amendments, new study submissions, and deviations; coordinate with PI and Management.
• Coordinate with Tissue Core, PRISM, and other shared resources to ensure recruitment, data and specimen collection are coordinated properly.
• Research coordinators can contribute to publications and assist with basic publication of results if applicable.

Skills

Verbal communication

Written communication

Critical thinking

Education

Associate’s degree in Public Health, Psychology, Biological Sciences or relevant field

Bachelor’s degree (1+ year of relevant research experience)

Master’s degree with no experience

Tools

PowerChart (EMR)

OnCore

REDCap

Job description

Working at Moffitt is both a career and a mission: to contribute to the prevention and cure of cancer.As the only National Cancer Institute-designated Comprehensive Cancer Center based in Florida, Moffitt employs some of the best and brightest minds from around the world. Join a dedicated team of nearly 11,000 who are shaping the future we envision. Moffitt has been recognized as a Best and Brightest Company to Work For in the Nation and is continually named one of the Tampa Bay Times’ Top Workplaces.SummaryThe primary focus of the NTRO Research Coordinator II role is to coordinate one or more non-therapeutic studies under the research portfolio of Dr. Vinci, Principal Investigator (PI). Coordination activities include study recruitment, enrollment, and other research activities. This position is expected to work under general supervision and direction from the supervisor and Principal Investigator to implement and coordinate research, including administrative procedures. This position is part of the NTRO research coordinator (RC) pathway.Ideal Candidate:Ability to plan, organize, and coordinate work assignments.Excellent verbal and written communication skills and the ability to adapt quickly and respond to the needs of the study team.Critical thinking skills and ability to solve issues with minimal guidance.Continues to build productive internal/external working relationships.Responsibilities: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 EDC system).Responsible for quality of the data coming in and ensuring that the protocol is being followed appropriately.Ability to handle a higher volume of moderate complex studies.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 on needs for the study; includes but is not limited to amendments, new study submissions, and deviations.Communication involves routinely convey 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.Research coordinators can contribute to publications and assist with basic publication of results if applicable.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.Salary Range$22.74 - $34.68Salary ranges posted for this position represent the expected base pay range for the role. Actual compensation may vary based on location and a variety of job-related factors, including experience, skills, education, and internal equity among Team Members in similar positions.We are committed to maintaining fair and equitable pay practices and regularly review compensation to ensure alignment across our workforce.Moffitt Career SiteIf you have the vision, passion, and dedication to contribute to our mission,then we have a place for you!1. Equal Employment OpportunityMoffitt Cancer Center is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, or protected veteran or disabled status. We seek candidates whose skills, and personal and professional experience, have prepared them to contribute to our commitment to diversity and excellence.2. Reasonable AccommodationFederal law requires employers to provide reasonable accommodation to qualified individuals with disabilities. Please tell us if you require a reasonable accommodation to apply for a job or to perform your job. Examples of reasonable accommodation include making a change to the application process or work procedures, providing documents in an alternate format, using a sign language interpreter, or using specialized equipment. Moffitt endeavors to make moffitt.org/careers accessible to any and all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process, please contact one of the Human Resources receptionists by phone at 813-745-7899 or by email at [e-mail]. This contact information is for accommodation requests only and cannot be used to inquire about the status of applications.Read more information about your EEO rights under the law.Transparency in Coverage Rule