ClinSkill

The course, Introduction to Clinical Research (ICR), covers the core areas of the clinical research is introduces you to the clinical research field and the core processes within it. This course is for students and professionals who wish to gain a basic understanding of the clinical research industry and process. 

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The course, 'Ethics in Clinical Research' covers the ethical perspectives of conducting clinical trials. The course will lay the foundation of conducting clinical research in an ethical manner and the processes, documents and guidelines that help achieve that. This course will cover the concepts of the Informed Consent process, ICH-GCP guidelines, Schedule-Y and ICMR guidelines amongst other aspects. 

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The Post Graduate Diploma in Clinical Research (PGDCR) covers the core areas of the clinical research process and equips you to start a career as a Clinical Research Professional. The course is aligned to the requirements of the industry and imparts clinical research process knowledge in a clear and concise manner so that you may kickstart a career in clinical research. 

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Oracle Clinical Fundamentals is an e-learning course that covers the  basic and advanced concepts of managing clinical trial data using the Oracle Clinical application. It is intended for students and clinical research professional who are willing to make a career in clinical data management using Oracle Clinical.  

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Oracle Remote Data Capture is an e-learning course that covers the process of conducting EDC studies using Oracle Remote Data Capture (RDC) tool. This course would be particularly useful to clinical research staff, nurses and site staff that are involved with data management at the site for Electronic Data Capture (EDC) studies. 

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The Professional Diploma in Clinical Data Management (PDCDM) is an eLearning Program that covers the management raw clinical data generated during clinical trials. The course imparts practical knowledge on clinical data management processes, documentation and workflow. It includes Hands-on Practical training on Oracle Clinical which is the de-facto standard for data mangagement used by most Fortune 500 companies today.

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Oracle Argus Safety Essentials is an e-learning course that covers the basic and advanced concepts of managing drug safety data using the Oracle Argus application. It is intended for students and clinical research professional who are willing to make a career in Pharmacovigilance using the Oracle Argus platform. 

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Oracle Argus Safety Console is a self-paced eLearning program that extensively covers the process of using the Argus Console module of Argus Safety for system configuration, business configuration and administration of the Oracle Argus Safety software. It is intended for drug safety professionals looking to expand their skillset and explore opportunities as Argus Safety Consultants and Argus Safety Support specialists. 

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Oracle Argus Safety Essentials + Console is an e-learning course that covers the basic and advanced concepts of managing drug safety data using the Oracle Argus application. It also covers the process of using the Argus Console module of Argus Safety for system configuration, business configuration and administration of the Oracle Argus Safety software. It is intended for students and clinical research professional who are willing to make a career in Pharmacovigilance using the Oracle Argus platform as well as drug safety professionals looking to expand their skillset and explore opportunities as Argus Safety Consultants and Argus Safety Support specialists. 

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Oracle Empirica Signal is an Oracle Health Science Application used for Signal Identification and Management from Adverse event data.

In this signal management course shall cover all the topics from detecting signals(Signal detection), through their validation and confirmation, analysis, prioritization and assessment to recommending action, as well as the tracking of the steps taken and of any recommendations made using the Oracle Empirica Signal application. 

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The Professional Diploma in Pharmacovigilance (PDPV) covers the core concepts of management of drug safety data and equips you to start a career in Pharmacovigilance domain. The course is aligned to the requirements of the industry and imparts  process knowledge of how drug safety data is management in a clear and concise manner so that you may kickstart a career in pharmacovigilance. 

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Oracle Argus Safety - Configuration and Administration is an e-learning course that covers the Business processes within Argus Safety while laying a strong focus on Configuration and Administration activities performed in Argus Safety. It is intended for professionals who are willing to make a career as an Argus Safety Implementation and Support Specialist.

This course will cover the topics outlined for the Oracle Argus Safety Certified Implementation Specialist Exam titled Oracle Argus Safety 8 Implementation Essentials 1Z0-473 and help you prepare for the same.

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The Professional Diploma in Medical Writing (PDMW) is an eLearning Program that has been tailor-made to enhance a participant's skill in medical writing. In this program you will learn and practice scientific writing, consumer health writing, medico-marketing writing and clinical research writing for regulatory authorities.

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The Professional Diploma in Medical Journalism (PDMJ) is an eLearning Program is a novel area of study which will enable you to design, implement, analyse, write, edit and manage research and other articles in the field of medicine and healthcare. The program will cultivate the skills required for you to work as a medical journalist. It will enable you to work at medical journals as Editors, or at medical research centres as research and publishing consultant. 

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The Professional Diploma in Regulatory Affairs (PDRA) is an eLearning Program that provides a thorough understanding of the various regulatory concepts and provide expertise in the field of regulatory affairs documentation and research. The course provides the knowledge you need to effectively manage the regulatory process during Innovation, Discovery, Approval and Commercialization stages of the drug.

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The Advanced Diploma in Clinical Research & Pharmacovigilance (ADCR-PV) covers the core areas of the Clinical research and Pharmacovigilance processes and equips you to start a career as a Clinical Research or Drug Safety professional. The course is aligned to the requirements of the industry and imparts clinical research and pharmacovigilance process knowledge in a clear and concise manner so that you may kickstart a career in clinical research and pharmacovigilance. This program includes hands-on training modules on Oracle Siebel Clinical - CTMS for Clinical Research and Oracle Argus Safety for Pharmacovigilance.

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The Advanced Diploma in Clinical Research & Data Management (ADCR-DM) is designed to provide students a complete understanding of clinical research and clinical data management processes. It equips you to start a career in Clinical Research Operations or as a Clinical Data Management professional. The course is aligned to the requirements of the industry and  includes hands-on training modules on Oracle Siebel Clinical - CTMS for Clinical Research and Oracle Clinical - CDMS for Clinical Data Management.

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The Advanced Diploma in Clinical Research & Medical Writing (ADCR-MW) is designed to provide you a complete understanding of the core areas of clinical research and medical writing. It equips you to start a career in Clinical Research Operations or as a Medical Writer. The course is aligned to the requirements of the industry provides comprehensive knowledge of all aspects of the curriculum.

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The Advanced Diploma in Clinical Research & Regulatory Affairs  (ADCR-RA) is designed to provide you a complete understanding of the core areas of clinical research and pharmaceutical regulatory affairs. It provides knowledge of global regulatory framework and develops skills required for regulatory strategy planning to ensure regulatory compliance. The course is aligned to the requirements of the industry and prepares you for the role of a regulatory affairs specialist for pre and post marketing studies.

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