Loretta Johnson Email and Phone Number
Loretta Johnson work email
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Loretta Johnson personal email
Clinical monitoring - Phase II, III, and IV Clinical trials.Specialties: Cardiovascular (coronary artery by-pass graft surgery, ST-elevation myocardial infarction, Stress myocardial perfusion imaging and Coumadin)Cardiovascular by-pass Stent (device study)Breast Agumentation (device study)Diabetes Mellitus (hypercholesterolemia)Pain (gout)Pain (adult migraines) Rheumatology (rheumatoid arthritis)Gynecology (post-menopausal) Hot flash Infectious Disease (Adult flu vaccine)Rare Disease
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Senior Cra /Functional Service ProviderIcon Strategic Solutions Mar 2024 - PresentUnited StatesVaccine Trial: A Phase III randomized double-blind controlled study to evaluate the immunogenicity, safety and reactogenicity of ExPEC9V and High-dose Quadrivalent Influenza Vaccine with and without Co-administration, in adults aged 65 years and Older.6 assign sites - Pre-study, SIV, MV, COV -
Senior Cra /Functional Service ProviderIcon Strategic Solutions Apr 2022 - Mar 2024United StatesDepression Treatment Resistant Trial: A randomized, double-blind, multicenter, placebo-controlled study to evaluate the efficacy, safety, and tolerability of Esketamine nasal spray, administered as monotherapy for treatment-resistant depression6 assigned sites - MV and COV -
Senior Cra / Functional Service ProviderIcon Strategic Solutions Mar 2020 - Mar 2022United StatesMultiple Sclerosis Trial: A phase III, double-blind efficacy and safety study comparing SAR442168 to participants with non-relapsing secondary progressive multiple sclerosis – Four sister protocols8 assigned sites - MV, COV -
Senior CraIcon Strategic Solutions Jul 2018 - Jul 2020United StatesIBS with Constipation Trial: Second phase III Randomized, 12-week, double-blind Placebo-Controlled Study of the Safety and Efficacy of XXX in patients with irritable bowel syndrome and Constipation (IBS-C)12 sites - Pre-study, SIV, IMV, COV -
Senior CraIcon Strategic Solutions Aug 2019 - Feb 2020Infectious Disease Trial: A Phase II Randomized and Controlled Investigation of Six Weeks of Oral XXX Therapy in Infants and Children with Congenital Cytomegalovirus Infection and Hearing Loss8 assigned sites - COV’s only -
Senior CraIcon Strategic Solutions May 2015 - Jun 2018United StatesCardiovascular Disease and Glucose Abnormalities Trial: A phase III trial to confirm the anti-anginal Effect of XXX in patients with stable angina.10 assigned sites - IMV, COV -
Senior CraIcon Strategic Solutions Dec 2013 - Apr 2015United StatesPost Menopausal Women with Vasomotor Symptoms Trial: A Phase II interventional trial, multi-center, double-blind, randomized, placeo-controlled multiple ascending dose study in post-menopausal women with vasomotor symptoms.5 assigned sites - Pre-study, SIV, IMV, COV -
Senior CraIcon Strategic Solutions Nov 2010 - Dec 2013United StatesType II Diabetes Trial: A Phased III multicenter, randomized, double-blind, Placebo-Controlled trial evaluating the safety and Efficacy XXX in subjects with Type 2 Diabetes with inadequately controlled hypertension.8 assigned sites - Pre-study, SIV, IMV, COV -
Clinical Research Associate IiAerotek Feb 2008 - Oct 2010United StatesCardiovascular Trial: Contract CRA II for IQVIA (formerly Quintiles), A Phase III, Randomized trial for treatment with a novel thienopyridine, prasugrel, compared with clopidogrel among patients undergoing planned percutaneous coronary intervention (PCI) for an acute coronary syndrome (ACS)Assisted with data cleaning (queries, site contact and follow-up) in preparation for database lock.2 assigned sites - IMV, COV -
Clinical Research Associate IiAerotek Jul 2007 - Jan 2008United StatesBreast Argumentation Device Trial: Contract CRA II for IQUIVA (formerly Quintiles), A Phase III trial, to assess outcomes, satisfaction and aesthetics of two different breast reconstruction techniques and compare its safety, patient satisfaction, aesthetic evaluation and complications1 site - pre-study, SIV, IMV, COV -
Clinical Research Associate IiIcon Strategic Solutions Jul 2004 - Jun 2007United StatesGeneral Gastrointestinal Trial: A Phase III study (General Gastrointestinal- IBS with constipation8 assigned sites – IMV, COV -
Cra IIcon Strategic Solutions Feb 2002 - Jul 2004United StatesHypertension with Type II Diabetes Trial: A Multicenter, randomized, double-blind, Placebo-Controlled, Phase III Trial evaluating the Safety and Efficacy XXX in subjects with Type 2 Diabetes with inadequately Controlled hypertension6 assigned sites - Pre-study, SIV, IMV, COV -
Clinical Trials Assistant (Cta)Icon Strategic Solutions Aug 2001 - Feb 2002Hypercholesterolemia Trial: An open label, randomized, Phase IIIb, study comparing the efficacy and safety of XXX in high-risk subjects with Type IIa and IIb Hypercholesterolemia Supported the administrative and logistical aspects of clinical trials for multiple studies ensuring the smooth operation and management of clinical studies
Loretta Johnson Skills
Loretta Johnson Education Details
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Bachelor Of Science - Bs
Frequently Asked Questions about Loretta Johnson
What company does Loretta Johnson work for?
Loretta Johnson works for Icon Strategic Solutions
What is Loretta Johnson's role at the current company?
Loretta Johnson's current role is Senior Clinical Research Associate.
What is Loretta Johnson's email address?
Loretta Johnson's email address is lo****@****plc.com
What schools did Loretta Johnson attend?
Loretta Johnson attended Tennessee State University.
What are some of Loretta Johnson's interests?
Loretta Johnson has interest in Global Taveling.
What skills is Loretta Johnson known for?
Loretta Johnson has skills like Gcp, Clinical Trials, Clinical Monitoring, Clinical Research, Ctms, Edc, Cro, Ich Gcp, Clinical Development, Oncology, Regulatory Submissions, Clinical Data Management.
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Loretta Johnson
Dacono, Co3msn.com, zayo.com, zayo.com2 +130338XXXXX
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1innovat.com
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Loretta Johnson
Vice President, Controls Quant Analytics Manager At Jpmorgan Chase & Co.Downers Grove, Il3yahoo.com, jpmchase.com, yahoo.com -
2cobham.com, baesystems.com
2 +160340XXXXX
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