Sandy Dunne

Sandy Dunne Email and Phone Number

Senior Clinical Trials Project Assistant @
Sandy Dunne's Location
Newtown, Pennsylvania, United States, United States
Sandy Dunne's Contact Details
About Sandy Dunne

Specialties: Clinical Trial Master Files, Veeva, Microsoft Office, ICH Guidelines, GCP, FDA, IRB, XPress, eTrack

Sandy Dunne's Current Company Details
PPD part of Thermo Fisher Scientific

Ppd Part Of Thermo Fisher Scientific

Senior Clinical Trials Project Assistant
Sandy Dunne Work Experience Details
  • Ppd Part Of Thermo Fisher Scientific
    Senior Clinical Support Specialist
    Ppd Part Of Thermo Fisher Scientific Dec 2021 - Present
    Collegeville, Pennsylvania, United States
    multiple sponsors
  • Ppd
    Senior Clinical Support Specialist
    Ppd Jun 2017 - Dec 2021
    Collegeville, Pennsylvania, United States
    for GSK
  • Inventiv Health Clinical
    Clinical Trial Specialist
    Inventiv Health Clinical Jun 2016 - Jun 2017
    Collegeville, Pennsylvania, United States
    for GSK
  • Mcneil Consumer Healthcare
    Clinical Trial Assistant (Fmd K&L)
    Mcneil Consumer Healthcare Sep 2015 - Jun 2016
  • Astrazeneca
    Clinical Study Associate (Real Staffing)
    Astrazeneca May 2014 - Jan 2015
    Wilmington, Delaware
  • Inventiv Health Clinical
    Clinical Trial Assistant (Pharmanet Resource)
    Inventiv Health Clinical Apr 2013 - Apr 2014
    Blue Bell, Pa
    ENDPOINT MANAGEMENT
  • Avid Radiopharmaceuticals, A Wholly Owned Subsidiary Of Eli Lilly And Co.
    Clinical Trial Assistant (Kelly Contractor)
    Avid Radiopharmaceuticals, A Wholly Owned Subsidiary Of Eli Lilly And Co. May 2012 - Mar 2013
    University City Science Center, Philadelphia, Pa 19104
    Contribute to lifecycle management of electronic and paper clinical study documentsAssist with study start-up activitiesEnsure compliance with regulatory guidance
  • Clinforce
    Tdos - Technical Document Operations Specialist (Contractor)
    Clinforce Mar 2011 - Feb 2012
    Spring House, Pa
    Created Site Binders, Electronically Filed Regulatory Documents for Multiple Studies, Audited and Remediated Hard Copy Files
  • Pfizer
    Senior Clinical Trial Associate
    Pfizer Jan 2004 - Jun 2010
    Collegeville, Pa
    Review and verify submission documentation for compliance according to Regulatory Authorities and company SOPs Coordinate document exchange with internal and external customers Archive documents in electronic and physical repositories Facilitate document request during regulatory inspectionsPrepare manuals and train workers in the use of new forms reports, procedures or equipment Ad hoc web page maintenance Facilitated vendor payments
  • Wyeth Pharmaceuticals
    Executive Administrative Assistant
    Wyeth Pharmaceuticals Jan 2001 - Dec 2003
    Managed office operations, calendar, travel arrangements correspondence, expense report and filesParticipated in pilot study for internal coding system for clinical trial documentation (DPIC)Processed incoming Serious Adverse Event reports with speed and accuracyInitiated meetings with peers to standardize processes across therapeutic areas
  • Wyeth Pharmaceuticals
    Senior Administrative Assistant
    Wyeth Pharmaceuticals Nov 1999 - Jan 2001
    Coordinated extensive international travel arrangements Prepared presentations for President Clinton and World Health Organization (WHO)
  • Apollon, Inc
    Executive Secretary Research & Development
    Apollon, Inc Jan 1996 - Nov 1999
    Managed office operations, schedules, travel and meeting planningCreated INDs and NDAsMaintained company libraryControlled access to laboratory notebooks Coordinated New Employee Orientation ProgramMaintained HR files and distributed payroll
  • Medical College Of Pennsylvania
    Executive Secretary
    Medical College Of Pennsylvania 1990 - 1996
    Philadelphia, Pennsylvania, United States
    Assisted Director of Biochemistry Education by preparing slides, tests and study material

Sandy Dunne Skills

Clinical Trials Gcp Pharmaceutical Industry Ctms Ich Gcp Clinical Development Sop Cro Good Clinical Practice Edc Biotechnology Regulatory Submissions Clinical Research Microsoft Office Vaccines Oncology Outlook Biochemistry Fda U.s. Food And Drug Administration Etmf Impact Documentum Document Review Irb Event Planning Medical Terminology Ophthalmology Oncology Clinical Research Neuroscience Asthma Travel Arrangements Regulatory Documentation Executive Administrative Assistance Executive Support Executive Calendar Management Wordstar Grant Preparation Scientific Papers Word Processing Ind Nda Payments Purchase Orders Microsoft Word Accounting Psychology Administrative Assistance Scientific Presentation

Sandy Dunne Education Details

Frequently Asked Questions about Sandy Dunne

What company does Sandy Dunne work for?

Sandy Dunne works for Ppd Part Of Thermo Fisher Scientific

What is Sandy Dunne's role at the current company?

Sandy Dunne's current role is Senior Clinical Trials Project Assistant.

What is Sandy Dunne's email address?

Sandy Dunne's email address is sa****@****ppd.com

What schools did Sandy Dunne attend?

Sandy Dunne attended Peirce College, Ursinus College.

What are some of Sandy Dunne's interests?

Sandy Dunne has interest in Poverty Alleviation, Travel, Genealogy, Gardening.

What skills is Sandy Dunne known for?

Sandy Dunne has skills like Clinical Trials, Gcp, Pharmaceutical Industry, Ctms, Ich Gcp, Clinical Development, Sop, Cro, Good Clinical Practice, Edc, Biotechnology, Regulatory Submissions.

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