Advanced Clinical Research Associate (CRA) Training Program

[kingers]

Advanced Clinical Research Associate (CRA) Training Program
Published 4/2025
MP4 | Video: h264, 1280x720 | Audio: AAC, 44.1 KHz, 2 Ch
Language: English | Duration: 4h 23m | Size: 1.91 GB

Clinical Research, Site Monitoring, Trial Management, CRA Career, Monitoring visit, ICH GCP, Clinical Trials, Regulatory

What you'll learn
Introduction to Clinical Research
CRA Roles & Responsibilities
Monitoring in Clinical Trials
Good Documentation Practices
Good Clinical Practices & 13 Principles of ICH GCP
Clinical Trial Monitoring
Clinical Research Associate
Site Monitoring
Site Selection Visit
Site Initiation Visit
Interim Monitoring Visit
Site Close-out Visit
Stakeholders in Clinical Research
Clinical Trial Site Management
CRA Career opportunities
CRA travel and functioning
Clinical Trial Audit and Inspections
Regulatory Submissions, Rules & Regulations
Phases of Clinical Trials: 1-2-3-4
Patient Recruitment in Clinical Research
Site Selection in Clinical Research
CRA Workload Management
Site Management & Multitasking skills
CRA Business travel & Management
Career mapping for Clinical Research Industry
Clinical Research Industry outlook and Growth opportunities for CRAs
CRA Career progression blueprint and guidance

Requirements
No prerequisite is needed for this course.
Basic understanding of Clinical Research would be helpful

Description
The Advanced Clinical Research Associate (CRA) Training Program is a thorough, industry-focused course aimed at providing participants with the key skills and knowledge needed to thrive as a Clinical Research Associate. This program is perfect for those looking to start or advance their careers in clinical research, including aspiring CRAs, healthcare professionals, life sciences graduates, and experienced industry veterans seeking to formalize their expertise.This program combines theoretical knowledge with practical application, covering essential aspects of Clinical trial management and Site Monitoring such as Types of monitoring visits (SSV, SIM, IMV & COV) along with Good Clinical Practice (GCP), regulatory requirements, ethical considerations, data management, and CRA monitoring. learners will gain a comprehensive understanding of the CRA's role in ensuring the integrity of the trial data and compliance of clinical trials from trial initiation to close-out.This course is led by experienced industry professional who has worked as a CRA extensively in his career. The course features real-world case studies, interactive modules, and hands-on training, ensuring learners are fully equipped to meet the demands of the CRA role. Upon successful completion, learners will earn a certification recognized across the clinical research industry, boosting their career prospects and professional credibility.Whether you're transitioning into clinical research or aiming to advance within the field, the Advanced CRA Training Program provides the tools and certification needed to succeed in this dynamic and rewarding profession.

Who this course is for
Students & Professionals exploring Career opportunities in Clinical Research
Clinical Research Coordinator (CRC) looking to transition into CRA role
Clinical Trial Assistant looking to transition into CRA role
Pharmacy graduates looking to start career as a CRA
Pharmacy, Biotechnology, Lifesciences, Chemistry & Medicine graduates looking to start career as a CRA
Anyone who want to understand the role and functioning of a Clinical Research Associate
Anyone who want to excel as a CRA and establish a strong fundamental understanding of the role

Homepage
https://www.udemy.com/course/advanced-clinical-research-associate-cra-training-program

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