required by protocol; evaluates patient response and complications; develops and revises patient care orders; educates and directs protocol compliance with physicians and staff nurses; assists in developing tools to meet requirements of new protocols; manages protocols with increased clinical complexities including translational investigator-initiated research as well as multi center trials; serves as clinical resource for other disease team members; collects and enters data for patients enrolled on protocol; participates in analyzing research data; communicates with outside federal or industry sponsors regarding protocol and patient status; assesses patient reaction to any modifications or treatment that are part of the protocol; provides educational and informational materials to study participants and their families about purposes, goals and objectives of study and what to expect as a study patient; responds to questions and concerns from patients about protocols; works with patients to ensure adherence with the protocol; serves as clinical resource for other disease team members.

Minimum Education Required: Bachelor's Level Degree or equivalent combination of education and experience with a Major in nursing

Required Qualifications: Bachelor's Degree in nursing required or equivalent combination of education and experience; current State of Ohio Nursing license or interim permit required.

Desired Qualifications: Clinical research certification from SoCRA (Society of Clinical Research Associates) or ACRP (Association of Clinical Research Professionals) preferred; experience in a clinical research capacity conducting clinical research trials preferred; considerable experience in providing direct patient care desired; experience in labor and delivery nursing desired; ability to work flexible hours (evenings) required.

required by protocol; evaluates patient response and complications; develops and revises patient care orders; educates and directs protocol compliance with physicians and staff nurses; assists in developing tools to meet requirements of new protocols; manages protocols with increased clinical complexities including translational investigator-initiated research as well as multi center trials; serves as clinical resource for other disease team members; collects and enters data for patients enrolled on protocol; participates in analyzing research data; communicates with outside federal or industry sponsors regarding protocol and patient status; assesses patient reaction to any modifications or treatment that are part of the protocol; provides educational and informational materials to study participants and their families about purposes, goals and objectives of study and what to expect as a study patient; responds to questions and concerns from patients about protocols; works with patients to ensure adherence with the protocol; serves as clinical resource for other disease team members.

Minimum Education Required: Bachelor's Level Degree or equivalent combination of education and experience with a Major in nursing

Required Qualifications: Bachelor's Degree in nursing required or equivalent combination of education and experience; current State of Ohio Nursing license or interim permit required.

Desired Qualifications: Clinical research certification from SoCRA (Society of Clinical Research Associates) or ACRP (Association of Clinical Research Professionals) preferred; experience in a clinical research capacity conducting clinical research trials preferred; considerable experience in providing direct patient care desired; experience in labor and delivery nursing desired; ability to work flexible hours (evenings) required.