Global Study Leader
Current
Apr 2018 - Present
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Barbara Kucharczyk Email & Phone Number
Global Study Leader at AstraZeneca
at
AstraZeneca
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✓ Verified July 2026
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Current company
Role
Global Study Leader at AstraZeneca
Location
Warsaw, Mazowieckie, Poland
Company size
Who is Barbara Kucharczyk? Overview
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Quick answer
Barbara Kucharczyk is listed as Global Study Leader at AstraZeneca at AstraZeneca, a with 59317 employees, based in Warsaw, Mazowieckie, Poland. AeroLeads shows a matched LinkedIn profile for Barbara Kucharczyk.
Barbara Kucharczyk previously worked as Global Study Leader at Astrazeneca and Regional Clinical Trial Manager at Amgen. Barbara Kucharczyk holds Postgraduate Study, Conducting And Monitoring Of Clinical Research from Akademia Leona Koźmińskiego W Warszawie.
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AstraZeneca
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Profile bio
About Barbara Kucharczyk
Seasoned professional with 14 years of experience in the clinical trials including CRO and pharmaceutical companies; confident in delivering projects on time and within budgets; quality focused with an excellent work ethics; good team player with great organizational and communication skills• multicultural exposure and direct cooperation with 15 countries on 5 continents• acted as mentor for 7 colleagues; shared knowledge and built their key competencies• delivered presentations during global investigators' meeting for up 150 participants• excellent audit outcomes: 12 audits with no major findings; prepared numerous sites for audits• full life cycle monitoring activities from start-up to close-out• therapeutic areas experience: CVRM, oncology, diabetes, inflammatory, respiratory, nephrology
Listed skills include Ich Gcp, Clinical Trials, Clinical Monitoring, Clinical Research, and 14 others.
Current workplace
Barbara Kucharczyk's current company
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Astrazeneca
7 roles
Barbara Kucharczyk work experience
A career timeline built from the work history available for this profile.
Regional Clinical Trial Manager
May 2016 - Apr 2018
Clinical Development Associate Manager
CDAM is a core member of a Study Team, responsible for end-to-end delivery of a clinical study on global level: Set-up phase• selection of participating countries • input into feasibility activities• preparation of study protocol, master consent form and operational documents• specification of systems to be used: electronic CRF, IVRS, ePRO, central lab etc.• content and conduct of international monitors and investigator meetings• development of investigator/monitor training materials and delivered presentation After First Site Initiation:• tracking and driving recruitment• supervision and management of patient recruitment• coordination of data cleaning• preparation of clinical study reportOverall duties:• primary point of contact for local study teams• regular communication with local study teams via e-mail, phone, regular TC• study progress oversight including submission & recruitment status, data cleaning• coordination & resolution of issues
Nov 2011 - Apr 2016
Study Associate
Therapeutic areas:oncology (pleural and peritoneal mesothelioma) – phase IIboncology (thyroid cancer) – phase IIIinflammatory (Crohn disease) – phase II ainflammatory (ulcerative colitis) – phase respiratory (asthma) – phase II bdiabetis – phase III
Dec 2010 - Oct 2011
Study Authorisation Associate
DOCS International Poland outsourced at ICON plc• preparation of submissions packages for the country specific RA & EC for the region• liaise with authorities regarding amendments & questions relating to start up activities• contact with the designated personnel from RA & EC to monitor the submission progress in accordance with study start up deadlines
May 2010 - Nov 2010
Clinical Trial Coordinator, Clinical Research Associate
Astellas Pharma
DOCS International Poland outsourced at: Astellas Pharma Poland Clinical Trial Administrator / Clinical Trial Coordinator / Clinical Research Associate• collection, completion and preparation of documents for the RA & EC• preparation of contracts for investigators and sites (adjustments to local conditions)• completion of documentation for the trials, including materials/documents for patients• coordination of study product distribution: • providing the sites with relevant documents • participation in routine activities in clinical trials monitoring in accordance with the ICH/GCP • check data entered to eCRFs• enter data to the Clinical Trial Management System• communication with the sites staff regarding the clinical trials• preparation and follow up activities associated with: Initiation and Monitoring visits• participation in audit preparation in accordance with ICH/GCP
Nov 2007 - Apr 2010
Clinical Trial Assistance
Jul 2006 - Oct 2007
Team & coworkers
Colleagues at AstraZeneca
Other employees you can reach at astrazeneca.com. View company contacts for 59317 employees →
EP
Estephany Pérez Gámez
Colleague at AstrazenecaMonterrey, Nuevo León, Mexico
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LA
Lyn Adanich
Colleague at AstrazenecaCleveland, Ohio, United States
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AP
Andrew Proffitt
Colleague at AstrazenecaNew Haven, Connecticut, United States
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SU
Sarahdines Undefined
Colleague at AstrazenecaCairo, Egypt
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AK
Aj Kinsella
Colleague at AstrazenecaKansas City, Missouri, United States
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RA
Ruben Alonzo
Colleague at AstrazenecaGreater Milan Metropolitan Area, Italy
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EV
Enrique Victor Hugo Diaz Aceves
Colleague at AstrazenecaGuadalajara, Jalisco, Mexico
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PG
Per Grönberg
Colleague at AstrazenecaNyköping, Södermanland County, Sweden
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PK
Pavan Kumar M
Colleague at AstrazenecaBengaluru, Karnataka, India
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DH
Dan Heathcote
Colleague at AstrazenecaStockport, England, United Kingdom
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Estephany Pérez Gámez
Colleague at AstrazenecaMonterrey, Nuevo León, Mexico
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LA
Lyn Adanich
Colleague at AstrazenecaCleveland, Ohio, United States
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AP
Andrew Proffitt
Colleague at AstrazenecaNew Haven, Connecticut, United States
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SU
Sarahdines Undefined
Colleague at AstrazenecaCairo, Egypt
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AK
Aj Kinsella
Colleague at AstrazenecaKansas City, Missouri, United States
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RA
Ruben Alonzo
Colleague at AstrazenecaGreater Milan Metropolitan Area, Italy
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EV
Enrique Victor Hugo Diaz Aceves
Colleague at AstrazenecaGuadalajara, Jalisco, Mexico
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PG
Per Grönberg
Colleague at AstrazenecaNyköping, Södermanland County, Sweden
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PK
Pavan Kumar M
Colleague at AstrazenecaBengaluru, Karnataka, India
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DH
Dan Heathcote
Colleague at AstrazenecaStockport, England, United Kingdom
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2 education records
Barbara Kucharczyk education
Postgraduate Study, Conducting And Monitoring Of Clinical Research
Master’S Degree, Master Degree In Institute Of Scientific Information And Librarian Studies
FAQ
Frequently asked questions about Barbara Kucharczyk
Quick answers generated from the profile data available on this page.
What company does Barbara Kucharczyk work for?
Barbara Kucharczyk works for AstraZeneca.
What is Barbara Kucharczyk's role at AstraZeneca?
Barbara Kucharczyk is listed as Global Study Leader at AstraZeneca at AstraZeneca.
Where is Barbara Kucharczyk based?
Barbara Kucharczyk is based in Warsaw, Mazowieckie, Poland while working with AstraZeneca.
What companies has Barbara Kucharczyk worked for?
Barbara Kucharczyk has worked for Astrazeneca, Amgen, Icon Plc, Astellas Pharma, and Parexel.
Who are Barbara Kucharczyk's colleagues at AstraZeneca?
Barbara Kucharczyk's colleagues at AstraZeneca include Estephany Pérez Gámez, Lyn Adanich, Andrew Proffitt, Sarahdines Undefined, and Aj Kinsella.
How can I contact Barbara Kucharczyk?
You can use AeroLeads to view verified contact signals for Barbara Kucharczyk at AstraZeneca, including work email, phone, and LinkedIn data when available.
What schools did Barbara Kucharczyk attend?
Barbara Kucharczyk holds Postgraduate Study, Conducting And Monitoring Of Clinical Research from Akademia Leona Koźmińskiego W Warszawie.
What skills is Barbara Kucharczyk known for?
Barbara Kucharczyk is listed with skills including Ich Gcp, Clinical Trials, Clinical Monitoring, Clinical Research, Gcp, Data Management, Ctms, and Oncology.
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