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.

1.5Month 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.

The Clinical Research Associate (CRA) Training Program at BCRI is designed to give you complete exposure to the clinical research process — from trial setup to regulatory compliance and study closure.

Whether you’re just starting or looking to switch careers, this job-focused training prepares you for real roles as a CRA or CRC.

📚 What You’ll Learn in This Program:

• Understand FDA regulations, ICH-GCP guidelines, and the ethics of clinical research
• Learn the full role and responsibilities of a CRA and CRC during clinical trials
• Master all four types of monitoring visits: pre-study, initiation, routine, and close-out
• Get insights into site selection, clinical trial agreements, and budget negotiation
• Explore informed consent procedures, and the role of IRBs (Ethics Committees)
• Develop skills in trial documentation, data integrity, and interim monitoring
• Understand safety reporting for drugs and devices — including SAE/AE management
• Learn site close-out, investigational product accountability, and audit preparedness
• Work through real-world case studies aligned with CRA/CRC job responsibilities

With practical training, mentor-led classes, and an optional internship, BCRI’s CRA Training Program helps you confidently enter the industry with job-ready skills and global awareness.

BCRI offers a wide range of clinical research and allied training programs in addition to the CRA Training Program. Depending on your background and career goals, you can explore:

👉 Advanced Diploma in Clinical Research (ADCR) – Includes Clinical Research, CDM & Pharmacovigilance

👉 PG Diploma in Clinical Research – Ideal for those seeking specialization in clinical operations and regulatory affairs, SAS or CRA/CRC.

👉 Clinical Data Management (CDM) Training – Learn data cleaning, CRF design, and validation tools

👉 Pharmacovigilance Training – Focused on drug safety reporting, signal detection, and global compliance

👉 SAS Clinical Programming Course – For those looking to enter data analysis in clinical trials

You can combine multiple programs or upgrade after CRA Training based on your career goals.