Data Coordinator - Hematology/Oncology

The Data Coordinator
plays a key role in managing the operational aspects of clinical research
studies throughout their lifecycle-from design and initiation to conduct and
closeout. In this position, you will oversee the implementation of research
activities for one or more studies, ensuring tasks are prioritized and completed
within required timelines. Responsibilities include planning and organizing
activities to maintain strict adherence to study protocols and applicable regulations,
including institutional policies, FDA Code of Federal Regulations (CFR), and
ICH Good Clinical Practice (GCP) standards. Work collaboratively with the Principal
Investigator (PI), ancillary departments, central research teams, sponsors, and
other stakeholders to support all facets of study administration. This includes
ensuring compliant study conduct, managing financial aspects, and coordinating
adequate personnel resources.

The full hourly salary
range for this position is $35.31 - $56.82.

Required:

* Bachelor's degree in related area and/or equivalent combination
of education and experience.

* Minimally 2+ years of previous study coordination or clinical
research coordination experience

* Interpersonal skills to effectively communicate information in a
timely, professional manner and establish and maintain cooperative and
effective working relationships with students, staff, faculty, external
collaborators and administration and to work as a member of a team.

* Ability to set priorities and complete ongoing tasks with
competing deadlines, with frequent interruptions, to meet the programmatic and
department needs, while complying with applicable University policies and
federal and state regulations.

* Analytical skills to assess clinical research protocols and
regulatory requirements, define problems, formulate logical solutions, develop
alternative solutions, make recommendations, and initiate corrective actions.

* Demonstrated proficiency with Adobe and Microsoft suite
software, especially Excel, to perform daily tasks efficiently and accurately.

* Working knowledge of clinical research concepts, policies and
procedures, and human safety protection regulations and laws.

* Knowledge of and experience working with a variety of local and
external IRBs, scientific review and other research committees, national
cooperative group sponsors, industry sponsors, federal and foundation funding
organizations, etc.

* High degree of concentration and focus in a work environment
that contains distracting stimuli, competing deadlines, and work delegated by
more than one individual

* Availability to work in more than one environment, travelling to
various clinic sites, meetings, conferences, etc.