CRA Training Program

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“With the most up-to-date Clinical Research Associate – CRA Training Program and innovative approaches to learning, we prepare our students for a successful career in Clinical Research.”

CRA Training course aims to equip you with the skills, knowledge, and experience required to become a Clinical Research Associate. Training will be provided by industry professionals who have been working in the field for years, and real-world examples will be provided so that you can apply what you learn in the classroom.

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Join a job-oriented training programme at BCRI with an excellent placement track record.
What we Teach in CRA Training Program?

You will gain practical experience performing clinical trials, analysing data, preparing reports, and performing other research-related tasks through hands-on work experience. A live online class taught by a Clinical Research Associates (CRA) professional will provide insight into CRA jobs and work environments.

Clinical Research Associate - CRA Training Program

CRA Training program is designed to ensure that you have the knowledge and proficiency needed for all stages of the clinical research process. From the design of clinical trials to their completion, this course will provide you with an in-depth look into all aspects of managing a clinical trial. You will learn how to design and implement site recruitment; review and analyze data collected during the trial; manage regulatory compliance issues; prepare documents according to regulatory requirements, conduct site closure activities, and more.

What you learn from CRA Training Program

The Clinical Research Associate (CRA) and Clinical Research Coordinator (CRC) are involved in Conducting Clinical Trials for any drug, biologics, and device.
CRA Training is an online Month Program to Start a career as CRA & CRC. CRA Training Program provides a comprehensive on Clinical Research and Drug Development, Ethics, Clinical Trial Monitoring, and much more.
Our Clinical Research Associates Training program is designed for individuals seeking a new career in clinical research or who want to change careers but aren’t sure which track to take. Many industry case studies and best practices are provided to demonstrate how the learning objectives relate to the responsibilities of CRAs and CRCs.

Course Description: 

  • Learn about FDA regulations, ICH guidelines, and Good Clinical Practice (GCP).
  • Explain the roles and responsibilities of a CRA and CRC.
  • Include an explanation of the four types of monitoring visits, including what the CRA and CRC are responsible for during the preparation, activity, and follow-up phases.
  • Pre-study Concepts: Principal Investigator, Site Selection, Clinical Trial Agreement, Budget Negotiation.
  • Defining informed consent requirements and the process of informed consent are discussed in relation to the role of the Institutional Review Board in clinical trials.
  • Data management, interim monitoring, and study site initiation are discussed.
  • Drugs and devices both need safety definitions and reporting requirements.
  • Conduct an examination of accountability for investigational products and study closeouts.
  • Examine how audits and inspections relate to regulatory compliance and quality assurance.
Join a Job oriented Training at BCRI, with Excellent Placement Track Record.
Learning Objective
  • Module 1: Investigational Product Development, the FDA, and Good Clinical Practice Guidelines
  • Module 2: Clinical Research Team: Roles and Responsibilities
  • Module 3: The Principal Investigator, Site Selection, and Budget Negotiation
  • Module 4: Clinical Study Protocol Elements
  • Module 5: Institutional Review Boards, the Consent of Human Volunteers, and HIPAA
  • Module 6: Study Monitoring, Data Management, and Study Initiation Visit
  • Module 7: Safety Reporting: Definitions and Reporting Requirements
  • Module 8: Accountability for the Test Article and Trial Termination Visits
  • Module 9: Regulatory Compliance and Quality Assurance: Audits and Inspections
  • Module 10: Managing Your Time and Preparing for the Interview
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FAQs About CRA Training Program

To become a Clinical Research Associate (CRA) needs to undergo a CRA training program that involves communication, relationship management, and Knowledge of clinical research and regulatory Guidelines. The CRA training program makes an individual expert in documenting protocols, adhering to regulations, and capturing site findings accurately ensuring the study’s quality and integrity.

Responsibilities include site monitoring, data verification, regulatory compliance, risk management, and ensuring the overall integrity of the clinical trial. As a CRA, you are the key bridge between management, the study site, and the sponsor. A stronghold in clinical research settings, good interpersonal skills, and a command of English are important. It is also critical and crucial to have fluency in the local language of the respective country you work in.

A clinical research associate (CRA) plans, prepares, and carries out clinical trials to test new or existing drugs, and devices, and assess their safety and benefits of use. The primary responsibilities of a CRA involve monitoring and ensuring the conduct of clinical trials per regulatory requirements and industry standards. CRA looks into Site Selection and Initiation, data collection, and documentation, Identify and assess potential risks and issues related to the conduct of the trial at investigational sites. The CRA training program makes him work stronger in this area.

  • The course is designed for aspiring Clinical Research Associates and Clinical Research Coordinators (it is also appropriate for new CRAs and CRCs with less than six months of experience).
  • People who are interested in careers in pharmaceuticals and clinical research can take this course. 
  • Those in college or just graduated with a degree in science
  • Nurses

Aspirants can get a CRA training program, where they gain a strong hold on pre-trial procedures, set up and organize clinical trial sites (with some supervision), and archive all the documents and correspondence. With the right combination of skills and experience you gain, can make a move into the role of senior CRA (SCRA), also known as a CRA

CRC facilitates the day-to-day operations of a clinical trial at the investigational site, working closely with the principal investigator and other study staff to ensure the smooth conduct of the trial, even in multiple sites

CRCs are responsible for the conduct and management of clinical trials at a particular site, whereas CRAs are involved with the regulatory and clinical oversight of multiple sites.

Aspirants interested in becoming a CRC can pursue a relevant, gain experience in a clinical or research setting program, and may consider certifications in clinical research coordination through a CRA/CRC training program. Applying for entry-level positions in clinical research or healthcare is a common starting point.

The responsibilities include patient recruitment, obtaining informed consent, data collection, maintaining documentation, communication with stakeholders, and overall coordination of activities at the investigational site and coordinating with multiple sites.

Similar to CRAs, CRCs typically need a bachelor’s degree in a relevant field with a proper CRA/CRC training program. Some employers may also value clinical research or coordination certifications.

The course duration is one month In- class.

20 Session of 1 hour Each

Clinical experience is beneficial with CRC training program, and also experience in a healthcare or research setting can enhance a candidate’s qualifications.

I should be hired for this clinical role because of my relevant skills in clinical research gained by the CRA training program, and my passion for the industry. I’ve researched the company profile and can add value to its growth. My positive attitude, hard work, and long-term goals align with the job requirements, making me a committed and valuable resource to the company.

The Clinical Research Associate (CRA) Training Program is designed to prepare you for the responsibilities of a clinical research professional. Through a series of interactive Sessions, each participant will gain knowledge and skills in the following areas: how to effectively communicate with prospective participants and investigators, how to develop study designs, gather and analyze data, design appropriate ethics statements for studies and evaluate data when needed.

Yes, we provide online clinical research courses for international students in countries like USA, Canada, and Australia. These courses are readily available over the internet, allowing students to access them in their own time and from the comfort of their homes.

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