Clinical Trials
First Job in Clinical Trials Program
Build a structured foundation in clinical trials and understand the main roles, documents, systems and processes before choosing your career path.
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LEARNING AREA SUBSCRIPTION
Clinical Trials Subscription
Build your clinical trials expertise with access to all courses and job-ready programs in this learning area. Get the latest course versions and new courses while your subscription is active.
33.25€/month
399.00€ billed annually
Access all 42 courses in Clinical Trials while your subscription is active.
- Latest course versions and new courses added to the learning area
- 8 job-ready programs included
- Course certificates and job-ready certificates
Everything included in your learning area
One subscription gives you the complete current learning area and keeps it up to date while your subscription is active.
JOB-READY PROGRAMS
Job-ready programs included
Choose any program in this learning area. Each program provides a focused 10-course curriculum and a job-ready certificate after completion.
Clinical Trials
Study Coordinator Program
Focus on the day-to-day conduct of clinical trials at the investigational site, including participants, documentation, protocol activities and monitor collaboration.
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Clinical Trials
Clinical Trial Assistant Program
Build focused knowledge of the documentation, systems and operational support activities used by Clinical Trial Assistants in sponsor and CRO study teams.
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Clinical Trials
Clinical Research Associate Program
Develop practical Clinical Research Associate (CRA) knowledge through 10 focused online courses covering site selection, initiation, monitoring, remote oversight and closeout.
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Clinical Trials
Clinical Documentation & TMF Specialist Program
Focus on Trial Master File management, document quality, inspection readiness and the systems and controls supporting clinical-trial records.
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Clinical Trials
Study Start-Up Associate Program
Build focused knowledge of the regulatory, documentation and site-readiness activities used to prepare clinical studies and sites for activation.
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Clinical Trials
Clinical Trial Quality Specialist Program
Focus on clinical-trial quality systems, CAPA, audit and inspection processes, document quality and inspection readiness.
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Clinical Trials
Clinical Trial Safety Specialist Program
Build structured knowledge of safety monitoring, SAE/SUSAR reporting and safety processes across the clinical trial lifecycle.
View programCOURSE LIBRARY
Explore all courses in this learning area
Open a course to review its content, duration and learning outcomes. Every course below is included while your subscription is active.
Courses included in this subscription
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Assessment and Medical Evaluation of ICSR
PharmacovigilanceClinical TrialsAleksandra Malicka
Certified by: -
Building an Effective SOP and Quality Management System (QMS) for Clinical Research Sites
Clinical TrialsLucas Dzioba -
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Effective collaboration between the Study Coordinator and the Clinical Research Monitor – Practical aspects of Monitoring Visits
Clinical TrialsErnest Szubert, Monika Czerwiński -
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Guidelines, regulations, and tools related to Trial Master File
Clinical TrialsKatarzyna PieńczukCertified by: -
Introduction to audit and inspection report
PharmacovigilanceClinical TrialsAgnieszka SokółCertified by: -
Introduction to bioequivalence of medicinal products
Clinical TrialsRegulatory AffairsJoanna Kupidura -
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Introduction to individual development plan
PharmacovigilanceClinical TrialsRegulatory AffairsMarcin Gołembski -
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Introduction to organized post-marketing data collection systems
PharmacovigilanceClinical TrialsMonika Nowak, Marek HurdaCertified by: -
Introduction to planning and performing monitoring visits
Clinical TrialsErnest SzubertCertified by: -
Introduction to Quality Management System
PharmacovigilanceClinical TrialsAgnieszka SokółCertified by: -
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Introduction to safety monitoring in clinical trials
PharmacovigilanceClinical TrialsMarek Hurda, Monika NowakCertified by: -
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Introduction to the management of ICSRs
PharmacovigilanceClinical TrialsAleksandra MalickaCertified by: -
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Management of an Investigational Product at a clinical site
Clinical TrialsErnest SzubertCertified by: -
Navigating EU CTR 536/2014 with transitioning from CTD
PharmacovigilanceClinical TrialsRegulatory AffairsKatarzyna Kopacz-Zakrzewska -
Practical aspects of Personal Data Protection in Pharmacovigilance and Clinical Trials
PharmacovigilanceClinical TrialsAnna Buczyńska-BorowyCertified by: -
Preparation to audits and inspections in clinical trials
Clinical TrialsAgnieszka SokółCertified by: -
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Transport of Biological Materials and IATA Rules in the Context of Clinical Research
Clinical TrialsMonika Czerwiński -
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Regulatory Affairs Subscription
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How to prepare case narrative and sender’s comment
PharmacovigilanceAleksandra MalickaCertified by: -
Courses included in this subscription
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Management of an Investigational Product at a clinical site
Clinical TrialsErnest SzubertCertified by: -
-
-
Introduction to Quality Management System
PharmacovigilanceClinical TrialsAgnieszka SokółCertified by: -
-
Practical aspects of Personal Data Protection in Pharmacovigilance and Clinical Trials
PharmacovigilanceClinical TrialsAnna Buczyńska-BorowyCertified by: -
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-
-
-
Assessment and Medical Evaluation of ICSR
PharmacovigilanceClinical TrialsAleksandra MalickaCertified by: -
-
-
-
-
-
Introduction to individual development plan
PharmacovigilanceClinical TrialsRegulatory AffairsMarcin Gołembski -
Introduction to safety monitoring in clinical trials
PharmacovigilanceClinical TrialsMarek Hurda, Monika NowakCertified by: -
Introduction to the management of ICSRs
PharmacovigilanceClinical TrialsAleksandra MalickaCertified by: -
-
-
Transport of Biological Materials and IATA Rules in the Context of Clinical Research
Clinical TrialsMonika Czerwiński -
-
-
-
-
Introduction to planning and performing monitoring visits
Clinical TrialsErnest SzubertCertified by: -
-
-
Guidelines, regulations, and tools related to Trial Master File
Clinical TrialsKatarzyna PieńczukCertified by: -
Building an Effective SOP and Quality Management System (QMS) for Clinical Research Sites
Clinical TrialsLucas Dzioba -
-
Navigating EU CTR 536/2014 with transitioning from CTD
PharmacovigilanceClinical TrialsRegulatory AffairsKatarzyna Kopacz-Zakrzewska -
-
-
Introduction to organized post-marketing data collection systems
PharmacovigilanceClinical TrialsMonika Nowak, Marek HurdaCertified by: -
-
Introduction to audit and inspection report
PharmacovigilanceClinical TrialsAgnieszka SokółCertified by: -
Introduction to bioequivalence of medicinal products
Clinical TrialsRegulatory AffairsJoanna Kupidura -
Preparation to audits and inspections in clinical trials
Clinical TrialsAgnieszka SokółCertified by: -
Effective collaboration between the Study Coordinator and the Clinical Research Monitor – Practical aspects of Monitoring Visits
Clinical TrialsErnest Szubert, Monika Czerwiński -