Job-ready Programs
Choose a focused program included in your learning area subscription.
Programs by learning area
Select a learning area to see the programs available in your subscription.
Every program ends with a job-ready certificate, on top of a certificate for each completed course. How certificates work
First Job in Pharmacovigilance Program
Build a structured foundation across the core processes, regulations and responsibilities that shape pharmacovigilance work.
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Safety Data Management Specialist Program
Build practical knowledge of ICSR intake, coding, assessment, database processing, case documentation and safety-data workflows.
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Local Pharmacovigilance Specialist Program
Build structured knowledge of local pharmacovigilance operations, oversight, literature, agreements, PSMF, risk management and compliance activities.
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Pharmacovigilance Quality Specialist Program
Build structured knowledge of PV quality systems, process oversight, CAPA, audits, agreements and key pharmacovigilance control points.
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Pharmacovigilance Medical Writing Specialist Program
Build structured knowledge of case narratives, CCSI, PSURs, RMPs, risk-minimisation content and clinical-development safety reports.
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First Job in Regulatory Affairs Program
Build a structured foundation in Regulatory Affairs and understand how medicines are registered, maintained and supported across their lifecycle.
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Regulatory Operations & Submissions Specialist Program
Focus on regulatory dossiers, CTD/eCTD structure, application documentation and the operational processes supporting regulatory submissions.
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Regulatory Product Information & Labelling Specialist Program
Focus on Product Information, labelling, mock-ups and the regulatory processes used to maintain and implement product-information changes.
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Local Regulatory Affairs Specialist Program
Build knowledge of the regulatory activities used to maintain products and support compliance at local affiliate and market level.
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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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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 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 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 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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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 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 Trial Safety Specialist Program
Build structured knowledge of safety monitoring, SAE/SUSAR reporting and safety processes across the clinical trial lifecycle.
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A learning area subscription includes all of its courses and job-ready programs.