Clinical Research Coordinator II

Franciscan Alliance, Inc.•Indianapolis, IN

1d•Onsite

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. 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.

Requirements

Associate degree required (Health Administration, Business, Health Science, Nursing/Patient Care preferred)
3 years research experience required
IF RN, 3 years Nursing/Patient Care required
IATA training within 6 months of hire date required
Certified Clinical Research Professional (CCRP) within 1.5 years required
Certified Clinical Research Coordinator (CCRC) within 1.5 years required

Nice To Haves

Bachelor's Degree preferred

Responsibilities

Collaborate with Research Financial Analyst to ensure research billing is accurate.
Conduct a thorough and ongoing informed consent process and document appropriately.
Conduct clinical trials that involve human subjects according to written protocols and departmental standards while adhering to Good Clinical Practice (GCP) Guidelines.
Create and complete valid source documentation per GCP requirements.
Document and maintain all research activities including patient visits.
Identify key elements of subject safety including, IRB oversight, study documentation, and event reporting.
Identify and explain key protocol elements to study subjects and perform study tasks as dictated by protocol.
Maintain research certification on a biannual or triannual basis, as appropriate.
Monitor adverse events and report serious events to the research sponsor according to written protocols and departmental standards.
Recruit and screen potential subjects for inclusion in clinical trials according to written protocols.
Respond to data queries issued by the study sponsor or sponsor's representative in a timely manner.