Elyssa Johnson Email & Phone Number
@quintiles.com
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Who is Elyssa Johnson? Overview
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Elyssa Johnson is listed as Local Trial Manager at IQVIA, based in Friendship, Wisconsin, United States. AeroLeads shows a work email signal at quintiles.com and a matched LinkedIn profile for Elyssa Johnson.
Elyssa Johnson previously worked as Senior Clinical Research Associate at Iqvia and Senior Clinical Research Associate at Iqvia. Elyssa Johnson holds Associate Of Science (A.S.), Registered Nursing/Registered Nurse from Rock Valley College.
Email format at IQVIA
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AeroLeads found 1 current-domain work email signal for Elyssa Johnson. Compare company email patterns before reaching out.
About Elyssa Johnson
Elyssa Johnson has been in the clinical research industry since 2010 as a research coordinator and Clinical Research Associate. Elyssa has participated in approximately 20 studies over the course of 5 years as a coordinator in the indications of oncology/hematology, in both cooperative group and pharmaceutical sponsored trials. Ms. Johnson joined Quintiles in 2015 as a Clinical Research Associate. She has experience in Phases I-III of clinical trials. She has electronic data capture experience. Ms. Johnson’s responsibilities as a CRA span the full duration of studies, from start-up to project closure. Ms. Johnson also has experience as a Lead CRA and performed Regional Lead/RCTM duties. She has experience as a CRA mentor and helped to teach oncology for CRAs and CRA1 classes.
Listed skills include Oncology, Clinical Research, Clinical Trials, Clinical Trial Management System, and 4 others.
Elyssa Johnson's current company
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Elyssa Johnson work experience
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Senior Clinical Research Associate
Senior Clinical Research Associate
Senior Clinical Research Associate
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.
Senior Clinical Research Associate
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 Associate Ii
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 Associate 2
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
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.
Clinical Research Coordinator And Nurse Navigator
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.
Registered Nurse
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
Infusion Nurse
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.
Inpatient Staff Nurse - Oncology
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.
Elyssa Johnson education
Associate Of Science (A.S.), Registered Nursing/Registered Nurse
Bachelor'S Degree, History
Frequently asked questions about Elyssa Johnson
Quick answers generated from the profile data available on this page.
What company does Elyssa Johnson work for?
Elyssa Johnson works for IQVIA.
What is Elyssa Johnson's role at IQVIA?
Elyssa Johnson is listed as Local Trial Manager at IQVIA.
What is Elyssa Johnson's email address?
AeroLeads has found 1 work email signal at @quintiles.com for Elyssa Johnson at IQVIA.
Where is Elyssa Johnson based?
Elyssa Johnson is based in Friendship, Wisconsin, United States while working with IQVIA.
What companies has Elyssa Johnson worked for?
Elyssa Johnson has worked for Iqvia, Psi Cro Ag, Pra Health Sciences, Syneos Health Clinical Solutions (Previously Inc Research/Inventiv Health), and Quintilesims.
How can I contact Elyssa Johnson?
You can use AeroLeads to view verified contact signals for Elyssa Johnson at IQVIA, including work email, phone, and LinkedIn data when available.
What schools did Elyssa Johnson attend?
Elyssa Johnson holds Associate Of Science (A.S.), Registered Nursing/Registered Nurse from Rock Valley College.
What skills is Elyssa Johnson known for?
Elyssa Johnson is listed with skills including Oncology, Clinical Research, Clinical Trials, Clinical Trial Management System, Protocol, Electronic Data Capture, Healthcare, and Nursing.
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