Clinical Research Coord II
Lafayette, INFull-time
Behavioral Health Market Context
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Job Description
thing 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
• Position required to report to the Hospital (some flexible remote hours)
• Collaborate with Research Financial Analyst to ensure research billing is accurate.
• Conduct clinical trials that involve human subjects, according to written protocols and departmental standards while adhering to Good Clinical Practice (GCP) Guidelines.
• Identify key elements of subject safety including, IRB oversight, study documentation, and event reporting.
• 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.
Qualifications
• Required Associate's Degree
• Preferred Associate's Degree Health Administration or Business
• Preferred Associate's Degree Health Science
• Preferred Associate's Degree Nursing / Patient Care
• Preferred Bachelor's Degree Health Science
• 3 years Research
Required
• 3 years Nursing/Patient Care if RN
Required
• IATA training within 6 months
Required
• Certified Clinical Research Professional (CCRP) - The Association of Clinical Research Professionals (ACRP)
• Certified Clinical Research Coordinator (CCRC) - The Association of Clinical Research Professionals (ACRP)
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 the benefit section of our career site, jobs.franciscanhealth.org.
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
• Position required to report to the Hospital (some flexible remote hours)
• Collaborate with Research Financial Analyst to ensure research billing is accurate.
• Conduct clinical trials that involve human subjects, according to written protocols and departmental standards while adhering to Good Clinical Practice (GCP) Guidelines.
• Identify key elements of subject safety including, IRB oversight, study documentation, and event reporting.
• 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.
Qualifications
• Required Associate's Degree
• Preferred Associate's Degree Health Administration or Business
• Preferred Associate's Degree Health Science
• Preferred Associate's Degree Nursing / Patient Care
• Preferred Bachelor's Degree Health Science
• 3 years Research
Required
• 3 years Nursing/Patient Care if RN
Required
• IATA training within 6 months
Required
• Certified Clinical Research Professional (CCRP) - The Association of Clinical Research Professionals (ACRP)
• Certified Clinical Research Coordinator (CCRC) - The Association of Clinical Research Professionals (ACRP)
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 the benefit section of our career site, jobs.franciscanhealth.org.
Qualifications
- •Required Associate's Degree
- •3 years Research
- •3 years Nursing/Patient Care if RN
- •IATA training within 6 months
- •Certified Clinical Research Professional (CCRP) - The Association of Clinical Research Professionals (ACRP)
- •Certified Clinical Research Coordinator (CCRC) - The Association of Clinical Research Professionals (ACRP)
Benefits
Responsibilities
- •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
- •Position required to report to the Hospital (some flexible remote hours)
- •Collaborate with Research Financial Analyst to ensure research billing is accurate
- •Conduct clinical trials that involve human subjects, according to written protocols and departmental standards while adhering to Good Clinical Practice (GCP) Guidelines
- •Identify key elements of subject safety including, IRB oversight, study documentation, and event reporting
- •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
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