PRN NTRO RESEARCH COORDINATOR II

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 10,000 who are shaping the future we envision.
Moffitt has been recognized as a Best and Brightest Company to Work for in the Nation, a Digital Health Most Wired Organization and continually named one of the Tampa Bay Time’s Top Workplaces.
A National Cancer Institute (NCI)-designated Comprehensive Cancer Center since 2001.

Summary

Position Summary:

The primary focus of the position is to participate in recruitment, inclusive of specimen and data collecting. Additional duties include coordinating studies of moderate complexity for assigned protocol(s). The data and specimen collection starts to increase in this role and this role starts to perform a limited amount of data entry. 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.

Position Highlight:

• Research coordinators can contribute to publications and assist with basic publication of results if applicable.
• This position is part of the research coordinator pathway, offering exciting opportunities for professional growth and development.

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.
• Ability to handle a higher volume of moderate complex studies.

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).
• Ensure the protocol is being followed appropriately and the quality of the data coming in is maintained.
• 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 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.

Credentials and Qualifications:

• Associate’s degree in Public Health, Psychology, Biological Sciences or relevant field with two (2) years of research or relevant experience required (may include time employed in a clinical or laboratory setting including roles such as scribe, clinical scheduling, medical assistant, laboratory or pharmacy technician); OR Bachelor’s degree requires at least one (1) year of research or relevant experience; OR Master’s degree no experience.
• ***A Hillsborough Community College (HCC) Associate Degree in Clinical Research can apply towards one (1) year of required research experience. This degree is 60 credit hours.

https://www.hccfl.edu/academics/subjects/health-and-medical/clinical-research-professional ***

• 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.