Clinical research monitor for Phase Ib-IV studies in the oncology, migraine, and GI therapeutic areas. Perform site selection, site initiation, monitoring, and closeout visits onsite and remotely. Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation. Provide study training to site staff. Experienced in Rave and InForm EDC systems. Experienced in Siebel, eClinical, and iMedidata CTMS systems.

Clinical research monitor for Phase Ib-IV studies in the oncology, migraine, and GI therapeutic areas. Perform site selection, site initiation, monitoring, and closeout visits onsite and remotely. Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation. Provide study training to site staff. Experienced in Rave and InForm EDC systems. Experienced in Siebel, eClinical, and iMedidata CTMS systems.

Clinical research monitor for Phase Ib-IV studies in the oncology, migraine, and GI therapeutic areas. Perform site selection, site initiation, monitoring, and closeout visits onsite and remotely. Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation. Provide study training to site staff. Experienced in Rave and InForm EDC systems. Experienced in Siebel, eClinical, and iMedidata CTMS systems.Syneos Health™ is the only fully integrated biopharmaceutical solutions organization. Our company,including a Contract Research Organization (CRO) and Contract Commercial Organization (CCO), ispurpose-built to accelerate customer performance to address modern market realities. Createdthrough the merger of two industry leading companies — INC Research and inVentiv Health — webring together more than 21,000 clinical and commercial minds with the ability to supportcustomers in more than 110 countries. Together we share insights, use the latest technologies andapply advanced business practices to speed our customers’ delivery of important therapies topatients. In short, we are shortening the distance from lab to life™.

Clinical research monitor for Phase Ib-IV studies in the oncology, migraine, and GI therapeutic areas. Perform site selection, site initiation, monitoring, and closeout visits onsite and remotely. Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation. Provide study training to site staff. Experienced in Rave and InForm EDC systems and Siebel CTMS.

Clinical Research Nurse Coordinator and mentor for new coordinators. Responsible for all aspects of subject management, from screening to data entry and query resolution for multiple oncology sites. Participated in cooperative group and industry-sponsored trials. Reviewed potential protocols to evaluate their suitability for study. Attended research meeting and conferences as required, and developed continuing education for other coordinators as part of the mentor activities.

Responsible for all aspects of subject management, from screening to data entry and query resolution for a network component oncology site. Participated in cooperative group trials through a collaboration with Loyola University in Maywood, IL. Reviewed potential protocols to evaluate their suitability for study. Attended research meeting and conferences as required. Also responsible for maintaining site-specific regulatory documents. As a nurse navigator, assisted oncology patients and their families through the treatment process by scheduling appointments, providing support and education, and referring to support services as needed.

Patient and family education, assessment and management of treatment side effects, telephone triage, rooming of patients, phlebotomy, administration of IV, IM, SQ medications as needed.Patient and family education, assessment and management of treatment side effects, telephone triage, rooming of patients, phlebotomy, administration of IV, IM, SQ medications as needed. Performed coordination of care between radiation, chemotherapy, and primary care offices

Patient and family education, telephone triage, assessment and management of side effects, coordination of care among specialties, Administration of IV, IM, SQ chemotherapy and supportive medications, growth factors, etc. Also served as facility OSHA officer until 5/2006. Served as nursing supervisor from 5/2006 to 10/2006.

Patient and family education, assessment and management of side effects, coordination of care among specialties, administration of IV, IM, SQ chemotherapy and supportive medications, growth factors, blood products, etc, central line care, admissions and discharges. Participated in the care of autologous stem cell transplant patients.