Paul Onuoha

Paul Onuoha Email and Phone Number

CRA at Celgene Corporation @ Celgene
86 Morris Avenue, Summit, New Jersey 07901, us
Paul Onuoha's Location
Sicklerville, New Jersey, United States, United States
Paul Onuoha's Contact Details

Paul Onuoha work email

Paul Onuoha personal email

About Paul Onuoha

Experienced Clinical Research Associate with over 6 years of direct site monitoring experience in the pharmaceutical industry. Over 4 years of experience working for a Clinical Research Organization monitoring all phases of clinical studies in various therapeutic areas concurrently. Very detailed oriented, strong interpersonal and communication skills and time management capabilities.Specialties: Oncology, Infectious Disease and Cardiovascular Disease

Paul Onuoha's Current Company Details
Celgene

Celgene

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CRA at Celgene Corporation
86 Morris Avenue, Summit, New Jersey 07901, us
Website:
celgene.com
Employees:
5
Paul Onuoha Work Experience Details
  • Celgene
    Sr. Cra
    Celgene Oct 2010 - Present
    Summit, New Jersey, Us
    - To make sure that the safety and well being trial subjects are protected- Monitoring the conduct of clinical studies, and monitoring of all types of site for compliance with GCP and SOP guidelines- Conduct site selection visits, initiation, routine, and close-out visits at investigator sites. - Monitoring the conduct of clinical studies, and monitoring of all types of site for compliance with GCP and SOP guidelines- Ensure accuracy of 1572 information, and ensure shipment of study-related materials.- Verify source to CRF’s and ensure accuracy; also ensure that corrections are made.- Monitor investigator sites for compliance in reporting AE and SAE
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  • Celgene Corporation
    Sr. Clinical Research Associate
    Celgene Corporation Oct 2010 - Present
    To make sure that the safety and well being trial subjects are protectedMonitoring the conduct of clinical studies, and monitoring of all types of site for compliance with GCP and SOP guidelinesConduct site selection visits, initiation, routine, and close-out visits at investigator sites. Monitoring the conduct of clinical studies, and monitoring of all types of site for compliance with GCP and SOP guidelinesEnsure accuracy of 1572 information, and ensure shipment of study-related materials.Verify source to CRF's and ensure accuracy; also ensure that corrections are made.Monitor investigator sites for compliance in reporting AE and SAE
  • Abraxis Bioscience
    Clinical Research Associate (Sr
    Abraxis Bioscience Feb 2009 - Present
    Los Angeles, Ca, Us
    To make sure that the safety and well being trial subjects are protectedMonitoring the conduct of clinical studies, and monitoring of all types of site for compliance with GCP and SOP guidelinesConduct site selection visits, initiation, routine, and close-out visits at investigator sites. Monitoring the conduct of clinical studies, and monitoring of all types of site for compliance with GCP and SOP guidelinesEnsure accuracy of 1572 information, and ensure shipment of study-related materials.Verify source to CRF's and ensure accuracy; also ensure that corrections are made.Monitor investigator sites for compliance in reporting AE and SAE
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  • Abraxis Bioscience
    Sr. Clinical Research Associate
    Abraxis Bioscience Feb 2009 - Oct 2010
    Los Angeles, Ca, Us
    - To make sure that the safety and well being trial subjects are protected- Monitoring the conduct of clinical studies, and monitoring of all types of site for compliance with GCP and SOP guidelines- Conduct site selection visits, initiation, routine, and close-out visits at investigator sites. - Monitoring the conduct of clinical studies, and monitoring of all types of site for compliance with GCP and SOP guidelines- Ensure accuracy of 1572 information, and ensure shipment of study-related materials.- Verify source to CRF’s and ensure accuracy; also ensure that corrections are made.- Monitor investigator sites for compliance in reporting AE and SAE
    View
  • Covance
    Clinical Research Associate
    Covance Aug 2007 - Jan 2009
    Princeton, New Jersey, Us
    To make sure that the safety and well being trial subjects are protectedMonitoring the conduct of clinical studies, and monitoring of all types of site for compliance with GCP and SOP guidelinesConduct site selection visits, initiation, routine, and close-out visits at investigator sites. Monitoring the conduct of clinical studies, and monitoring of all types of site for compliance with GCP and SOP guidelinesEnsure accuracy of 1572 information, and ensure shipment of study-related materials.Verify source to CRF's and ensure accuracy; also ensure that corrections are made.Monitor investigator sites for compliance in reporting AE and SAE
    View
  • Orion Clinical Services
    Clinical Research Associate Ii
    Orion Clinical Services Oct 2005 - Aug 2007
    Merthyr Tydfil, Wales, Gb
    Conduct site selection visits, initiation, routine, and close-out visits at investigator sites. Monitoring the conduct of clinical studies, and monitoring of all types of site for compliance with GCP and SOP guidelinesEnsure accuracy of 1572 information, and ensure shipment of study-related materials.Train site staff on protocol issues that arise frequently.Close all outstanding queries during a close out visit.Communicated trial progress to the project team on a monthly basis.
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Paul Onuoha Skills

Data Storage Usa Laboratory Iec Monitors Supplies Clinical Trials Source Jersey Human Resources Herpes Informed Consent Cardiovascular Solid Tumor Listings Site Visits Fix Protocol History Kidney Breast Sae Infectious Diseases Adverse Events Clinical Research Reviews Irb Cell Home English Ovarian Guidelines Clinical Research Associates Materials Heart Disease Reports Information System Sop Orion Safety Compliance Verifying Template Initiation Clinical Services Exceptions Subjects Oncology Queries Location Intelligence Gcp Concord Pancreatic Case Report Forms Therapeutic Area Mrsa Project Management Wellbeing Documentation Melanoma Trains And Add Rails System Monitoring Reporting Aes Investigation Nsclc Hiv Evaluation Bioscience Resolve

Paul Onuoha Education Details

  • The George Washington University
    The George Washington University
    Clinical Research Administration
  • New Jersey Institute Of Technology
    New Jersey Institute Of Technology
    Information System
  • The George Washington University
    The George Washington University
    Clinical Research Management

Frequently Asked Questions about Paul Onuoha

What company does Paul Onuoha work for?

Paul Onuoha works for Celgene

What is Paul Onuoha's role at the current company?

Paul Onuoha's current role is CRA at Celgene Corporation.

What is Paul Onuoha's email address?

Paul Onuoha's email address is pa****@****hoo.com

What schools did Paul Onuoha attend?

Paul Onuoha attended The George Washington University, New Jersey Institute Of Technology, The George Washington University.

What skills is Paul Onuoha known for?

Paul Onuoha has skills like Data Storage, Usa, Laboratory, Iec, Monitors, Supplies, Clinical Trials, Source, Jersey, Human Resources, Herpes, Informed Consent.

Who are Paul Onuoha's colleagues?

Paul Onuoha's colleagues are Taneisha Bouler, Cesur Cekirge, Scott Smith, Joe Alicea, Bikash Jha, Bob Goria, Jo Laina.

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