Great Online Training Provides Online Training in CDM Course. We have certified trainers to tech CDM. This CDM course covers the syllabus for CDM certification. This course training is completely E-Learning Instructor Lead Training.
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Duration of the Course depends which batch you are join Regular Batch or Weekend batch Regular Batch: To complete this course in Regular batch 30 days and per week 5 days (TUESDAY TO SATURDAY DAY). Daily 1 hour will be the classWeekend batch: To complete this course in Weekend batch 12 days and per day 3 hours (SATURDAY DAY and SUNDAY).
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- Life science graduates
- Bachelors in Dental
- Bachelors & Masters in Pharmacy
- Graduates in Math, Computers, Statistics
What Is Clinical Data Management (CDM)?
Clinical data management is the process by which important data is collected, integrated, analyzed, and validated while researchers conduct clinical trials. Medical and pharmaceutical companies and organizations, as well as regulatory groups, push toward higher standards and quality assurance. This leads to a pronounced need for individuals and systems who provide CDM services.
Clinical data management training must prepare workers to conduct the services they provide with the utmost professionalism and attention to detail. A CDM expert processes many types of research data that come out of clinical trials pertaining to medical and treatment advancements. The job requires proficiency with various computer applications and database systems. Besides handling the digital technology surrounding the collected data, clinical data managers must also understand how to validate and clean the data so it is accurate and appropriate for the researchers' needs.
The most important aspects of a clinical data management job entail:
- Ensuring accuracy of all clinical data
- Checking for complete data to facilitate accurate outcomes
- Making sure the collected data follows a logical path
- Maximizing consistency to weed out discrepancies and errors
All of these practices help researchers know that the data they use to conduct future studies or make conclusions on their theories are sound and accurate.
What Role Does a Clinical Data Manager Play in Clinical Trials?
The entire data management process involves various steps and responsibilities required for accurate clinical trial operations and completion. The primary activity involves delivering the most accurate data that supports the final results of the study. This end goal requires a multi-step process to ensure integrity, consistency, and validity of every piece of appropriate data.
CDM professionals usually work as part of a team. The specialists collect and compile results from various medical or pharmaceutical studies. Bachelor's or even Master's degrees are required for the various stages of clinical data management careers, though a CDM course provides appropriate skill brush up and familiarization.
Besides simply collecting and reviewing data, these management professionals must understand and follow all appropriate regulations in order to make sure the clinic or research facility does not experience any blocks or issues with official organizations like the FDA.
Top Companies Offering Jobs in Clinical Data Management
A search through online job boards and approaching recruiters for the medical, clinical research, and pharmaceutical industries may result in quite a lot of clinical data management jobs for those who finished appropriate CDM courses. The following six organizations offer considerable opportunity for properly-educated and high-skilled professional data managers.
TCS – TATA Consultancy Services
Instead of directly providing clinical data management teams, TCS specializes in the current transformation of data collection and analysis processes to more digitized methods. Still, all the hospital and clinical wearable devices or sensors cannot exist without the help of the human touch. They are primarily interested in CDM specialists with a focus on Business 4.0 understanding and capabilities.
This international company focuses on improving and extending lives through appropriate clinical and other research trials in both medical and pharmaceutical specialties. In order for the data to inform improvements and innovation, professional CDM team members must collect and handle data in conjunction with new digital and AI systems.
As one of the global leaders in CDM, IQVIA offers opportunities to those who successfully completed appropriate clinical data management training. Their interests transcend managing numbers and bits of information. They look for experts who can handle all of it properly and add the all-important touch of human insight to a modern process of data management.
With locations in Massachusetts and North Carolina, this data management company offers career opportunities for excellent CDM professionals from a diverse range of nations. They focus on both the heart and mind when it comes to delivering the best possible outcomes from every research study and trial they work with. This makes clinical data management that much more important.
A combination of managing collected data and their innovative Intent data collection digital device makes them one of the forerunners of the new data revolution in medicine and healthcare. Clinical data management specialists required working knowledge of how to collect, validate, and handle digitized research information.
Why the CDM Job Market is So Popular
Both the medical and pharmaceutical industries constantly conduct a variety of research studies to improve treatment plans and medications for people suffering from everything from epilepsy to cancer to heart disease and beyond. These studies will not provide solutions if the data collected from them fail to get used in an appropriate manner.
This makes clinical data management training of the utmost importance for the advancement of healthcare and disease treatment around the world. The CDM job market is so popular because the world of research creates more data all the time, and someone has to ensure its accuracy, usability, organization, and compliance with all necessary regulations.
What Is the Difference Between CDM and SAS?
CDM stands for clinical data management and involves collecting data from more than one research trial and integrating it with similar data collections in order to create a fuller and more accurate picture.
SAS stands for statistical analysis software and it takes the clinical or research data, analyzes it digitally, and generates various reports or charts that the researcher or other organization can use to form decisions.
In many instances, CDM and SAS go hand in hand in practical application. The management professionals that do the human side of data collection sometimes use SAS programs to then deliver the final, organized, and understandable report.
When it comes to jobs in the industry, clinical data management hires people who perform the particular collection and cross-checking services, and SAS requires programmers who create the systems.
Clinical Data Management Jobs vs. Medical Coding Jobs
In the medical field, every diagnosis, treatment options, medical procedure, piece of equipment, and provided service has a unique alphanumeric code. When a patient's records are created and finalized, a medical coder transforms any documentation or notes into this code. This job usually has something to do with filing for insurance payments. The highly trained professionals must maintain complete accuracy.
Clinical data managers collect and process data instead of transforming it into universal medical codes. If they get the information from a research study or other clinical trial, gather it together with other trials' data, and validate it for accuracy and relevance, the medical coding specialist may then turn it into the letter and number codes that represent the processes used.
Each career provides valuable services to the medical community and health-related industries. They both need considerable training to gain employment and succeed.
What Are Clinical Trials?
Whenever a medical researcher, organization, or company wants to develop a new treatment or medication, they need to do a lot of lab-related research before they get to clinical trials that test them out on real people. The process of developing an appropriate clinical trial goes through a lot of steps and involves regulations from many sides. After all, a researcher cannot perform random experiments on people without certain safety assurances in place.
The various reasons for clinical trials include:
- Testing of pharmaceuticals for help and safety
- New medication forms: pills, capsules, liquids, etc.
- Existing drugs that may have alternate uses
- Evaluating vitamins, minerals, herbs, and other supplements
- Tests to see if treatments or procedures can give a positive outcome
- Attempts to find new ways to track diseases
Whoever designs a clinical trial has to go through a lot of regulatory details before they can find study participants. They choose the scientists or medical professionals to help, get approval by government organizations, the Institutional Review Board, and whatever corporation or agency is funding the study, to begin with.
Clinical Trial Stages Explained
Every clinical trial must go through the following four phases. These ensure that everything is tested properly to get the best and safest possible outcome.
The first round of pharmaceutical testing must include at least 10 people with adequate health. These Human Pharmacology Trials give researchers the first information about whether a particular mediation or treatment is safe, does not have excessive side effects, and if it demonstrates therapeutic change.
The Therapeutic Exploratory Trials increase the number of research subjects. This phase of a clinical trial is designed to test if a drug is effective and safe for the people it is intended to treat. Each medication gets tested against a placebo.
This wide-spread research study usually includes thousands of study participants who test the drug for a longer period of time. This expands the research pool to various countries, age groups, ethnicities, and other demographic characteristics.
At this point, the new medication has been approved for use. This Post Marketing Surveillance phase has more to do with figuring out how to sell the drug rather than if it works well or not. Each medication gets compared to similar drugs on the market. Of course, researchers keep looking for unexpected side effects.
What Is the CDM Process?
The process involved in clinical data management follows the same basic steps no matter what type of research studies and data are involved. Of course, the modalities may change from one company or organization to the next.
Study Document Review and Finalization
The team identifies the data types, figures out what they will collect, and determines how best to format the data itself. This focuses on consistency and intuitive structure. Then, the CDM team creates a Data Management Plan (DMP) that clearly states the road map to move forward with the project.
Design the Databases
CDMs do not type everything into a spreadsheet and call it a day. The databases they design are project-specific, partially automated, and involve both the DMP rules and outside regulations and requirements. They create databases to make the data collection and investigation process more organized and efficient.
User Acceptance Test (UAT) of Databases
Before data can be collected in a study, the clinical database has to be developed and tested by Clinical data manager.
Collect the Data
What used to happen with paperwork now primarily occurs using digital methods. With either method, the data from various studies or sources gets combined into the system. This helps eliminate errors and locate discrepancies quickly.
The case report forms (CRF) for each project are under control of the CDM team for storage, retrieval, and tracking throughout the process. This ensures the safety of the data so nothing gets left out of the final valuation.
For paper-based Clinical trials, CRF data will be entered into the Clinical database by Clinical data entry person.
Validating the Data
Each DMP has certain protocols in place to make sure all the data is valid and appropriate for the clinical data management project. If the team finds any discrepancies, the quality control investigators take over.
A Data Clarification Form (DCF) is created for any discrepancies and managed in the specific way appropriate for a particular project. This process is also named query resolution and is ongoing throughout the process.
All records appropriate for the particular CDM project is transformed into regulated medical coding. This ensures proper understanding across the board and maintains consistency in data and any comments or additional reports.
Once the Clinical Data Management team ensures a clean and error-free clinical database, the team locks the database to prevent any further changes in the database. This process requires agreement by everyone involved with the CDM project.
CDM Team Roles and Responsibilities
Every clinical data management project involves a team of individuals that work together to get the best and most accurate outcome possible. They need advanced education, proper training, medical knowledge, and IT or computer skills.
Different Clinical Data Management Roles
- Data manager
- Database design and programming expert
- Clinical data coder
- Clinical data coordinator
- Quality control associate
- Data entry personnel
Responsibilities of the CDM Project Team
Besides the complexities of collecting, validating, organizing, and otherwise using all the data from specific medical or clinical trials, the clinical data management team also interacts with study sponsors, sticks to deadlines, and handles all operational issues that may arise.
The Clinical Data Management training course will help you prepare for this complex and important role.
- Life cycle of a drug 00:00:00
- Phases of Clinical trials 00:00:00
- Priniciples of ICH-GCP 00:00:00
- Good Clinical data management practices 00:00:00
- Sub parts of 21 CFR Part 11 00:00:00
- Different components of Protocol 00:00:00
- Importance of Protocol in Clinical Trials 00:00:00
- CRF Completion Guidelines 00:00:00
- DM Activities in Study Set up Part-I 00:00:00
- Different Conduct activities in CDM 00:00:00
- Discrepancy Management Process 00:00:00
- Types of Discrepancy 00:00:00
- Paper & EDC Study 00:00:00
- Overview of Process 00:00:00
- How to handle Safety data in CDM Process 00:00:00
- Different steps involved in Close out activities- Part I 00:00:00
- How to create CV for different jobs in CDM 00:00:00
- To Talk on Existing Experience 00:00:00
- How you can get certification for this course 00:00:00