Maxim Pashnin Md Ccra
Over 14 years of clinical research experience including all aspects of study management as well as audit preparation... | Auckland, Auckland, New Zealand
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Maxim Pashnin Md Ccra’s Emails ma****@iq****.com
Maxim Pashnin Md Ccra’s Phone Numbers No phone number available.
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Maxim Pashnin Md Ccra’s Location Auckland, Auckland, New Zealand
Maxim Pashnin Md Ccra’s Expertise Over 14 years of clinical research experience including all aspects of study management as well as audit preparation and monitoring, investigator/patient recruitment, protocol and CRF development, SOP writing, and development of study specific educational and promotional materials. Considerable research interests and experience in multiple therapeutic areas including Pulmonology, Gastroenterology, CNS, Cardiology, Infectious diseases (Hepatitis C, COVID-19), Oncology, Virology, Vaccines, Autoimmune diseases, Pain management, Dermatology, Diabetes and pediatrics among others. Extensive experience working with different types of organizations such as academic institutions (Rush University, University of Louisville, University of Iowa), sponsor companies (Pfizer, GSK, Takeda, Metabolex, Celgene, Ardea, Bayer, Roche, AMAG, Salix, Exact Sciences, Synergy etc.), CROs (ICON, PPD, Covance, Quintiles, PAREXEL, PRA International, INC Research, etc.) and labs (Covance, ICON, Quest, Quintiles). Proficient working with EDC (Medidata, Medidata Rave, DATATRAK, Oracle, Perceptive etc.), CTMS (PMED, Impact) and IVR/IWR systems. Specialties: - Study Management/Monitoring and Safety reporting; - Site/SMO Audit preparation US/Canada; - Development and maintenance of study protocols, plans, trackers, CRF, SOP, etc.; - Knowledge of GCP/ICH and FDA regulations; - Selection and training of investigator sites; - Planning and running study meetings; - Timely enrollment of qualified patients; - Data cleanup and completion of study
Maxim Pashnin Md Ccra’s Current Industry Iqvia
Maxim
Pashnin Md Ccra’s Prior Industry
Roche Pharmaceuticals
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Bayer
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Canadian Centre For Clinical Trials
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Dm Clinical Research Clinical Trials In Partnership With The Texas Center For Drug Development
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Parexel
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Continuum Clinical
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Abbvie
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Novo Nordisk Via Syneos Health
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Iqvia
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Synteract
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Work Experience
Iqvia
Sr. Clinical Research Associate
Fri Apr 01 2022 00:00:00 GMT+0000 (Coordinated Universal Time) — Wed May 01 2024 00:00:00 GMT+0000 (Coordinated Universal Time)
Synteract
Sr. Clinical Research Associate
Sun Aug 01 2021 00:00:00 GMT+0000 (Coordinated Universal Time) — Tue Mar 01 2022 00:00:00 GMT+0000 (Coordinated Universal Time)
Iqvia
Sr. Clinical Research Associate
Thu Nov 01 2018 00:00:00 GMT+0000 (Coordinated Universal Time) — Tue Jun 01 2021 00:00:00 GMT+0000 (Coordinated Universal Time)
Novo Nordisk Via Syneos Health
Senior Clinical Research Associate
Sun Apr 01 2018 00:00:00 GMT+0000 (Coordinated Universal Time) — Thu Nov 01 2018 00:00:00 GMT+0000 (Coordinated Universal Time)
Abbvie
Clinical Research Associate
Sun Nov 01 2015 00:00:00 GMT+0000 (Coordinated Universal Time) — Sun Apr 01 2018 00:00:00 GMT+0000 (Coordinated Universal Time)
Continuum Clinical
Clinical Enrollment Specialist
Wed Oct 01 2014 00:00:00 GMT+0000 (Coordinated Universal Time) — Sat Aug 01 2015 00:00:00 GMT+0000 (Coordinated Universal Time)
Parexel
Clinical Enrollment Manager
Tue Jan 01 2013 00:00:00 GMT+0000 (Coordinated Universal Time) — Tue Apr 01 2014 00:00:00 GMT+0000 (Coordinated Universal Time)
Dm Clinical Research Clinical Trials In Partnership With The Texas Center For Drug Development
Sr. Clinical Research Coordinator
Wed Aug 01 2012 00:00:00 GMT+0000 (Coordinated Universal Time) — Tue Jan 01 2013 00:00:00 GMT+0000 (Coordinated Universal Time)
Canadian Centre For Clinical Trials
Clinical Research Coordinator
Mon Dec 01 2008 00:00:00 GMT+0000 (Coordinated Universal Time) — Sun Jul 01 2012 00:00:00 GMT+0000 (Coordinated Universal Time)
Bayer
Clinical Trials Monitor
Thu Jan 01 2004 00:00:00 GMT+0000 (Coordinated Universal Time) — Fri Apr 01 2005 00:00:00 GMT+0000 (Coordinated Universal Time)
Roche Pharmaceuticals
Medical Representative
Mon Apr 01 2002 00:00:00 GMT+0000 (Coordinated Universal Time) — Thu Jan 01 2004 00:00:00 GMT+0000 (Coordinated Universal Time)Skills
Languages
Maxim Pashnin Md Ccra Email Addresses
FAQ About Maxim Pashnin Md Ccra
-
Maxim Pashnin Md Ccra is located at
Auckland, Auckland, New Zealand -
Maxim Pashnin Md Ccra is a
Over 14 years of clinical research experience including all aspects of study management as well as audit preparation and monitoring, investigator/patient recruitment, protocol and CRF development, SOP writing, and development of study specific educational and promotional materials. Considerable research interests and experience in multiple therapeutic areas including Pulmonology, Gastroenterology, CNS, Cardiology, Infectious diseases (Hepatitis C, COVID-19), Oncology, Virology, Vaccines, Autoimmune diseases, Pain management, Dermatology, Diabetes and pediatrics among others. Extensive experience working with different types of organizations such as academic institutions (Rush University, University of Louisville, University of Iowa), sponsor companies (Pfizer, GSK, Takeda, Metabolex, Celgene, Ardea, Bayer, Roche, AMAG, Salix, Exact Sciences, Synergy etc.), CROs (ICON, PPD, Covance, Quintiles, PAREXEL, PRA International, INC Research, etc.) and labs (Covance, ICON, Quest, Quintiles). Proficient working with EDC (Medidata, Medidata Rave, DATATRAK, Oracle, Perceptive etc.), CTMS (PMED, Impact) and IVR/IWR systems. Specialties: - Study Management/Monitoring and Safety reporting; - Site/SMO Audit preparation US/Canada; - Development and maintenance of study protocols, plans, trackers, CRF, SOP, etc.; - Knowledge of GCP/ICH and FDA regulations; - Selection and training of investigator sites; - Planning and running study meetings; - Timely enrollment of qualified patients; - Data cleanup and completion of study Iqvia -
Maxim Pashnin Md Ccra currently works in the
Iqvia -
Maxim Pashnin Md Ccra specializes in
Over 14 years of clinical research experience including all aspects of study management as well as audit preparation and monitoring, investigator/patient recruitment, protocol and CRF development, SOP writing, and development of study specific educational and promotional materials. Considerable research interests and experience in multiple therapeutic areas including Pulmonology, Gastroenterology, CNS, Cardiology, Infectious diseases (Hepatitis C, COVID-19), Oncology, Virology, Vaccines, Autoimmune diseases, Pain management, Dermatology, Diabetes and pediatrics among others. Extensive experience working with different types of organizations such as academic institutions (Rush University, University of Louisville, University of Iowa), sponsor companies (Pfizer, GSK, Takeda, Metabolex, Celgene, Ardea, Bayer, Roche, AMAG, Salix, Exact Sciences, Synergy etc.), CROs (ICON, PPD, Covance, Quintiles, PAREXEL, PRA International, INC Research, etc.) and labs (Covance, ICON, Quest, Quintiles). Proficient working with EDC (Medidata, Medidata Rave, DATATRAK, Oracle, Perceptive etc.), CTMS (PMED, Impact) and IVR/IWR systems. Specialties: - Study Management/Monitoring and Safety reporting; - Site/SMO Audit preparation US/Canada; - Development and maintenance of study protocols, plans, trackers, CRF, SOP, etc.; - Knowledge of GCP/ICH and FDA regulations; - Selection and training of investigator sites; - Planning and running study meetings; - Timely enrollment of qualified patients; - Data cleanup and completion of study -
Maxim Pashnin Md Ccra speaks the following languages:
No languages available. -
Maxim Pashnin Md Ccra has prior experience in the following industries:
Iqvia , Synteract , Iqvia , Novo Nordisk Via Syneos Health , Abbvie , Continuum Clinical , Parexel , Dm Clinical Research Clinical Trials In Partnership With The Texas Center For Drug Development , Canadian Centre For Clinical Trials , Bayer , Roche Pharmaceuticals -
Maxim Pashnin Md Ccra has the following professional experience:
Iqvia , Synteract , Iqvia , Novo Nordisk Via Syneos Health , Abbvie , Continuum Clinical , Parexel , Dm Clinical Research Clinical Trials In Partnership With The Texas Center For Drug Development , Canadian Centre For Clinical Trials , Bayer , Roche Pharmaceuticals . -
You can view Maxim Pashnin Md Ccra’s
LinkedIn profile at LinkedIn URL. -
Maxim Pashnin Md Ccra’s work email addresses are
[email protected] . -
Maxim Pashnin Md Ccra works at
Iqvia
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