Clinical Research Coordinator II - Impactful Trials

Franciscan Health Indianapolis Campus 8111 S Emerson Ave Indianapolis, Indiana 46237 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 Schedule: Monday - Friday, 8am - 5pm 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. QUALIFICATIONS Associate degree required (Health Administration, Business,Health Science, Nursing/Patient Care preferred ) Bachelor’s Degree 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 TRAVEL IS REQUIRED: Never or Rarely EQUAL OPPORTUNITY EMPLOYER It is the policy of Franciscan Alliance to provide equal employment to its employees and qualified applicants for employment as otherwise required by an applicable local, state or Federal law. Franciscan Alliance reserves a Right of Conscience objection in the event local, state or Federal ordinances that violate its values and the free exercise of its religious rights. Franciscan Alliance is committed to equal employment opportunity. Franciscan provides eligible employees with comprehensive benefit offerings. Find an overview on thebenefit section of our career site, jobs.franciscanhealth.org . #J-18808-Ljbffr