Sara Skok
Over 20 years of experience in clinical research industry which includes 14 years of experience monitoring in Phase... | Minneapolis, Minnesota, United States
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Sara Skok’s Emails sa****@pp****.com
Sara Skok’s Phone Numbers No phone number available.
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Sara Skok’s Location Minneapolis, Minnesota, United States
Sara Skok’s Expertise Over 20 years of experience in clinical research industry which includes 14 years of experience monitoring in Phase I-IV clinical drug trials , including post market and medical device studies, 3 years of Lead CRA that included management responsibilities and 7 years of study management lead experience including unblinded lead roles, oncology, Phase 1 studies and experience with biotech clients. Management oversight of regional monitoring team for 2 Mega Trials ( 4+ yrs, approx 10,000 patients) with CRO- inclusive of study start up from SSV, SIV, IMV to final DBL. Management of team for final close out of sites, eTMF reconciliation & full IP accountability. Successful final data base lock within agreed timelines of sponsor.
Sara Skok’s Current Industry Iqvia
Sara
Skok’s Prior Industry
Ppd Medical Device
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Graftcath
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Atritech
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Quintiles
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Ppd
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Bright Research Partners
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Parexel
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Pra Health Sciences
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Iqvia
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Work Experience
Iqvia
Senior Clinical Lead
Wed Sep 01 2021 00:00:00 GMT+0000 (Coordinated Universal Time) — Present
Pra Health Sciences
Clinical Trial Manager
Sat May 01 2021 00:00:00 GMT+0000 (Coordinated Universal Time) — Thu Jul 01 2021 00:00:00 GMT+0000 (Coordinated Universal Time)
Parexel
Clinical Operations Lead
Wed Aug 01 2018 00:00:00 GMT+0000 (Coordinated Universal Time) — Sat May 01 2021 00:00:00 GMT+0000 (Coordinated Universal Time)
Bright Research Partners
Consultant
Thu Feb 01 2018 00:00:00 GMT+0000 (Coordinated Universal Time) — Sun Jul 01 2018 00:00:00 GMT+0000 (Coordinated Universal Time)
Ppd
Clinical Team Manager
Fri Aug 01 2014 00:00:00 GMT+0000 (Coordinated Universal Time) — Mon Jan 01 2018 00:00:00 GMT+0000 (Coordinated Universal Time)
Ppd
Sr. CRA
Wed Jun 01 2011 00:00:00 GMT+0000 (Coordinated Universal Time) — Fri Aug 01 2014 00:00:00 GMT+0000 (Coordinated Universal Time)
Quintiles
Sr. Clinical Research Associate
Mon Oct 01 2007 00:00:00 GMT+0000 (Coordinated Universal Time) — Tue Feb 01 2011 00:00:00 GMT+0000 (Coordinated Universal Time)
Atritech
CRA
Tue Nov 01 2005 00:00:00 GMT+0000 (Coordinated Universal Time) — Wed Aug 01 2007 00:00:00 GMT+0000 (Coordinated Universal Time)
Graftcath
CRA
Sun May 01 2005 00:00:00 GMT+0000 (Coordinated Universal Time) — Tue Nov 01 2005 00:00:00 GMT+0000 (Coordinated Universal Time)
Ppd Medical Device
CRA
Thu Apr 01 2004 00:00:00 GMT+0000 (Coordinated Universal Time) — Sun May 01 2005 00:00:00 GMT+0000 (Coordinated Universal Time)
Ppd Medical Device
Research Coordinator
Thu Apr 01 2004 00:00:00 GMT+0000 (Coordinated Universal Time) — Sat Jan 01 2005 00:00:00 GMT+0000 (Coordinated Universal Time)Skills
Languages
Sara Skok Email Addresses
FAQ About Sara Skok
-
Sara Skok is located at
Minneapolis, Minnesota, United States -
Sara Skok is a
Over 20 years of experience in clinical research industry which includes 14 years of experience monitoring in Phase I-IV clinical drug trials , including post market and medical device studies, 3 years of Lead CRA that included management responsibilities and 7 years of study management lead experience including unblinded lead roles, oncology, Phase 1 studies and experience with biotech clients. Management oversight of regional monitoring team for 2 Mega Trials ( 4+ yrs, approx 10,000 patients) with CRO- inclusive of study start up from SSV, SIV, IMV to final DBL. Management of team for final close out of sites, eTMF reconciliation & full IP accountability. Successful final data base lock within agreed timelines of sponsor. Iqvia -
Sara Skok currently works in the
Iqvia -
Sara Skok specializes in
Over 20 years of experience in clinical research industry which includes 14 years of experience monitoring in Phase I-IV clinical drug trials , including post market and medical device studies, 3 years of Lead CRA that included management responsibilities and 7 years of study management lead experience including unblinded lead roles, oncology, Phase 1 studies and experience with biotech clients. Management oversight of regional monitoring team for 2 Mega Trials ( 4+ yrs, approx 10,000 patients) with CRO- inclusive of study start up from SSV, SIV, IMV to final DBL. Management of team for final close out of sites, eTMF reconciliation & full IP accountability. Successful final data base lock within agreed timelines of sponsor. -
Sara Skok speaks the following languages:
No languages available. -
Sara Skok has prior experience in the following industries:
Pra Health Sciences , Parexel , Bright Research Partners , Ppd , Ppd , Quintiles , Atritech , Graftcath , Ppd Medical Device , Ppd Medical Device -
Sara Skok has the following professional experience:
Iqvia , Pra Health Sciences , Parexel , Bright Research Partners , Ppd , Ppd , Quintiles , Atritech , Graftcath , Ppd Medical Device , Ppd Medical Device . -
You can view Sara Skok’s
LinkedIn profile at LinkedIn URL. -
Sara Skok’s work email addresses are
[email protected] . -
Sara Skok works at
Iqvia
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