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Krasucki
Email: jk965548@westpost.net
Telephone: 610-505-5139
11 Landover Drive
Coatesville, PA 19320
Education:
2008 to current Drexel University, M.S. Clinical Research Organization &
Management (18 credits to date)
9/2003-5/2005 Widener University, B.A. Magna Cum Laude (Psychology, Sociolo
gy)
9/2001-5/2003 Harcum College, A.A. with high honors (Liberal Studies)
Awards, Honors and Membership:
2007-2008 MDS Charities Committee
2007-present SoCRA - Society for Clinical Research Associates
2005 Pi Gamma Mu Honor Society
2005 Phi Kappa Phi Society
2005 Alpha Chi Honor Society
2004 Psi Chi Honor Society
2003-2005 Academic Scholarship
2003 Harcum Award - Best All Around Student
2003 Who's Who among American Junior Colleges
2002 Phi Theta Kappa Society
Professional Experience:
Pfizer / Wyeth Pharmaceuticals - Consultant for Inventiv Clinical Solutions
1/2009- Current Global Trial Management Assistant
Provided in-house support to assigned project teams.
* Participated in project meetings, including meeting minute preparation, team d
istribution, and upload to EDMS (electronic document management system).
* Developed monthly and quarterly project newsletters.
* Facilitated global supply (e.g. binders, DIRs, protocols) upkeep and DHL distr
ibution to RSMs.
* Coded large volumes of Regulatory documents for upload to EDMS, Maintained stu
dy team Roster in IMPACT and project FAQ.
* Provided assistance on Audit responses.
* Created and maintained multiple study eRoom's content and access rights.
* Provided additional support activities as delegated (e.g. creation of project
spreadsheets, filtering large spreadsheets for necessary information, processin
g/tracking CDAs and CSAs, facilitate Clinicaltrails.gov updates).
Additional Training:
* AMS (Agreement Management System) Training, July 2009
* Regional Study Manager New Hire Training, Sept. 2009. 4 days of presentations
covering the RSM role and responsibilities, global study file management, site
selection and pre-study, SM assignment process, study start-up, IVRS, vendor man
agement, payment process, RSM technology, informed consent, GCPs and trip report
review.
MDS Pharma Services
8/2008 - 12/2008 Clinical Research Associate
2/2008- 8/2008 Sr. Clinical Trials Associate
10/2007- 1/2008 Clinical Trials Associate II
6/2007- 10/2007 Clinical Trials Associate
Provided support to assigned project teams including information management, and
in-house and on site monitoring.
* On -site monitoring and off site management of 5 eastern region sites on CNS t
rial
* Assisted with the development of project status reports (e.g. enrollment, esse
ntial document reports).
* Participated in project meetings, including meeting minute preparation and ass
igned site status review.
* Initiated, tracked and reviewed investigator payments and financial informatio
n.
* Prepared, collected and reviewed regulatory and essential documents.
* Facilitated IRB/IEC submission and approval process.
* Set-up and maintained data tracking systems.
University of Pennsylvania -
School of Medicine, Dept. of Psychiatry, Center for Weight and Eating Disorders