Clinical Research Coordinator-1
About The Position
Clinical research helps improve medical treatments and care standards. It’s not a job filled with test tubes (at least not all the time) – it’s a perfect balance of working with patients, researchers and medical professionals. A thriving research program, like at Franciscan, needs support and coordination for everything from preparing participants to creating result charts and graphs. WHO WE ARE Franciscan Health is a leading healthcare organization dedicated to providing exceptional patient care and promoting health and wellness in our community. Our mission is to ensure that every patient receives the highest quality of care through innovation, compassion, and excellence. With 12 ministries and access points across Indiana and Illinois, Franciscan Health is one of the largest Catholic health care systems in the Midwest. Franciscan Health takes pride in hiring coworkers who provide compassionate, comprehensive care for our patients and the communities we serve. WHAT YOU CAN EXPECT Abstract data and complete Case Report forms, in accordance with Sponsors' and Department's written standards. Prepare for and participate in monitoring and auditing activities, including scheduling, document preparation, and issue resolution. Complete initial regulatory paperwork, including required essential documents, submissions to the research administration, and submissions to the IRB. Complete regulatory requirements for changes in research, including submission to the research administration, submission to the IRB, and communication to the research team. Monitor protocol deviations and violations, and report events to the research sponsor, according to written protocols and departmental standards. Respond to and resolve data queries, in accordance with Sponsors’ and Department’s written standards.
Nice To Haves
- Associate's Degree Nursing / Patient Care
- 1 year Healthcare Administration (Business)
- 1 year Nursing/Patient Care
- 1 year Research Administration
Responsibilities
- Abstract data and complete Case Report forms, in accordance with Sponsors' and Department's written standards.
- Prepare for and participate in monitoring and auditing activities, including scheduling, document preparation, and issue resolution.
- Complete initial regulatory paperwork, including required essential documents, submissions to the research administration, and submissions to the IRB.
- Complete regulatory requirements for changes in research, including submission to the research administration, submission to the IRB, and communication to the research team.
- Monitor protocol deviations and violations, and report events to the research sponsor, according to written protocols and departmental standards.
- Respond to and resolve data queries, in accordance with Sponsors’ and Department’s written standards.
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Education Level
Associate degree
Number of Employees
1-10 employees
