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CRA Full course Training includes ✓ CRA Base ✓CRA Advance ✓CRA certification Training ✓✓Resume ✓Mock Interview ✓Job Assistance

Welcome to Great Online Training, your one-stop destination for top-notch Clinical Research Associate (CRA) training. Our comprehensive online courses are specifically designed to equip you with the skills and knowledge you need to excel in the rapidly growing field of clinical research. With our expertly curated content, flexible learning schedules, and personalized support, you'll be well on your way to becoming a successful CRA.

Course Details

Course Name Clinical Research Associate (CRA)
Duration 40 days / 1 Hr per day
Training Days Monday to Friday
Live Class Recordings Access Provided
Materials Life Time Access
Resume Preparation Included In The Course
Interview Preparation Q&A Will Be Provided
Certificate Course Completion Provide
These days the health care sector is growing in a fast manner and this is not just the sector growing rapidly but the CLINICAL RESEARCH industry also is enlarging the industry especially in the Covid-19 pandemic. People understood the important role of Indian clinical research industry in pandemic time which helped to fight against the Covid-19 by coming up with the vaccine.

 

What is Clinical research associate?

Clinical Research associate is a person who is employed by Pharmacy Company or a contract research organization to ensure the drugs are safe by taking clinical trials to test drugs and check their side effects, benefits and effectiveness. 

How to Enroll in this course?

STEP - 1: Register Below
Please register for a free demo session by filling in your details in the below form and choose a suitable time to take the demo session.

Enroll For A Free Demo

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After completion of step 1 you will get a confirmation mail to your registered mail id immediately. In that mail you will get all the information about our course fee and other details.

  • Step 3: Call from Training Co-ordinator

After that you will get a mobile call or Whatsapp call from our training coordinator to explain all the details of our training course and any questions or doubts from your side will be cleared. If you have any technical questions then you will be forwarded to our Python trainer from great online training, you can ask your career related doubts before you start your career in Python.

  • Step 4: CRA Free Demo

After completion of a call from our coordinator you will be invited for our CRA free demo session by Great online training. You will receive a mail or a message to your registered number. You can attend 3 to 4 classes for free after that if you want to continue with our training classes then you have to move to the next step.

  • Step 5: Payment of Fee

After you decide to continue with our training course you need to do a fee payment through PayPal / Xoom / Net banking / western union/ UPI / DEBIT Card / CREDIT Card Payment on the same day. After completion of payment you will receive the material, software, and daily classes recording video folder. You will be added to your batch mate’s whatsapp group and you can attend the live sessions daily through the same link which is shared in the group. Now you can continue you training classes.

Roles and Responsibilities:

  • CRA should select or choose an investigator who is responsible for test trials at the site.
  • Maintain the communication with doctors or consultants about conducting the trails.
  • Training the staff as per the standards of operating procedure for clinical trials.
  • Ensure that the trail site includes like trial materials, trial drug are set up. 
  • Verifying that investigator and their team are adequately trained or not according to the protocol.
  • Monitoring the trail site throughout the specified duration.
  • Source data verification
  • Collecting trail documentation and preparing reports.

Why Choose Our CRA Training Program ?

Expertly Designed Curriculum:

Our course content is meticulously crafted by industry professionals with years of experience in clinical research, ensuring that you receive the most up-to-date and relevant information. Our curriculum covers essential topics such as clinical trial management, regulatory compliance, data management, and pharmacovigilance.

Flexible Learning Options:

We understand that every learner has unique needs and schedules. That's why our online CRA training program allows you to learn at your own pace, with 24/7 access to course materials and resources. Whether you're a full-time professional or a busy student, you can easily fit our training into your schedule.

Engaging Learning Experience:

At Great Online Training, we believe that learning should be engaging and enjoyable. Our interactive lessons, multimedia content, and real-world case studies will keep you motivated and actively involved throughout the course.

Personalized Support:

Our dedicated team of instructors and support staff is committed to your success. From answering your questions to providing personalized feedback on assignments, we're here to help you every step of the way.

Comprehensive Assessment and Certification:

Upon completion of our CRA training program, you'll be assessed through a series of quizzes, assignments, and a final exam to ensure that you've mastered the necessary skills. Successful candidates will receive a Certificate of Completion, validating your expertise and opening doors to new career opportunities.

Networking and Job Assistance:

As a part of our commitment to your success, we offer networking opportunities with fellow students and professionals, as well as job placement assistance to help you kickstart your career as a Clinical Research Associate.

Career Opportunities:

Nearly 50K clinical research professionals are required in clinical research industry and this sector is becoming one of the most popular options. One of the main points about a career in clinical research is that candidates do not need to come from a medical background to start their career in this field.  With IT background also candidates can opt for clinical research careers.  They can be hire for poisions like Business Development, Clinical Project Management and study data to predict the seriousness of the disease, research data to evaluate the efficiency of a new medicine or vaccine, and many such pivotal roles.

  • Lead CRA
  • Head of clinical research
  • Project Manager
  • Director of clinical operations.

There are so many career opportunities for clinical research associate in pharmaceutical and health care sectors. Depending on experience in this candidates can aspire to be above positions.

Clinical Research Associate Jobs Eligibility

To be eligible for a Clinical Research Associate (CRA) job, candidates must typically meet the following requirements:

1. Education: A bachelor's degree in life sciences, nursing, pharmacy, or a related field is generally required. Some employers may prefer candidates with a master's degree or a higher level of education in a relevant discipline.

2. Experience: Entry-level CRA positions typically require 1-2 years of experience in clinical research, such as working as a clinical research coordinator, study coordinator, or research assistant. For more senior CRA roles, several years of experience as a CRA or in a similar role within the clinical research industry is often required.

3. Clinical Research Training: Completion of a clinical research associate training program or a relevant course that covers good clinical practice (GCP), clinical trial regulations, study design, data management, and other essential aspects of clinical research is highly desirable. Some employers may require specific certifications, such as the Certified Clinical Research Associate (CCRA) designation from the Association of Clinical Research Professionals (ACRP) or the Society of Clinical Research Associates (SoCRA).

4. Skills: CRAs must possess strong organizational, communication, and interpersonal skills, as they need to interact effectively with site personnel, sponsors, and regulatory authorities. Attention to detail, problem-solving, and the ability to manage multiple tasks and priorities are also important skills for a CRA.

5. Familiarity with Regulations and Guidelines: A thorough understanding of relevant regulations and guidelines, such as the International Council for Harmonisation (ICH) GCP guidelines and regional regulatory requirements (e.g., FDA regulations in the United States), is essential for a CRA role.

6. Computer Skills: Proficiency in using standard software applications, such as Microsoft Office Suite, and familiarity with clinical trial management systems and electronic data capture (EDC) systems is usually required.

7. Language Skills: Fluency in the local language(s) of the clinical trial sites is important, as CRAs often need to communicate with site personnel and review study documents in the local language. Proficiency in English is also generally required, as it is the most commonly used language in international clinical research.

8. Willingness to Travel: CRAs must be willing to travel frequently to conduct site visits, as monitoring clinical trial sites is a major part of their job responsibilities. This may involve domestic and international travel, depending on the locations of the study sites.

Meeting these eligibility criteria will improve your chances of securing a job as a Clinical Research Associate. However, individual employer requirements may vary, so it's essential to review specific job postings and tailor your application accordingly.

Clinical Research Associate  Job Titles

The job title "Clinical Research Associate" (CRA) may encompass various roles and responsibilities within the clinical research field, depending on the employer and the specific job description. Some alternative or related job titles for a CRA may include:

1. Clinical Trial Monitor

2. Clinical Trial Associate

3. Clinical Study Monitor

4. Clinical Research Coordinator (CRC) – although this role is typically more site-focused, some organizations may use the title interchangeably with CRA.

5. Clinical Research Specialist

6. Clinical Site Manager

7. Regional Clinical Research Associate

8. Lead Clinical Research Associate

9. Senior Clinical Research Associate

10. Clinical Operations Associate

These job titles may have slightly different responsibilities or focus areas, depending on the organization and the specific clinical trials being conducted. However, they generally involve tasks such as site selection, site initiation, site monitoring, and site closeout, as well as ensuring compliance with good clinical practice (GCP), study protocols, and regulatory requirements.

Clinical Research Associate  Job Organizations

Clinical Research Associates (CRAs) can find job opportunities in various organizations within the clinical research industry. Some of the main organizations that employ CRAs include:

1. Pharmaceutical companies: CRAs may work in-house for large or small pharmaceutical companies, managing and monitoring clinical trials for investigational drugs.

2. Biotechnology companies: Similar to pharmaceutical companies, biotechnology companies also conduct clinical trials for the development of novel therapies and products, employing CRAs to manage and monitor these trials.

3. Contract Research Organizations (CROs): CROs provide a wide range of services to pharmaceutical, biotechnology, and medical device companies, including clinical trial management and monitoring. CRAs working for CROs may have the opportunity to work on various projects for different clients.

4. Medical device companies: CRAs may work for medical device companies, overseeing clinical trials for new medical devices or monitoring post-market surveillance studies.

5. Academic research institutions and hospitals: Some CRAs may work in academic settings, managing and monitoring clinical trials conducted by researchers at universities, hospitals, or research centers.

6. Non-profit organizations and government agencies: CRAs may also find employment with non-profit organizations or government agencies involved in clinical research, such as the National Institutes of Health (NIH) in the United States.

7. Clinical trial management companies: Some companies specialize in providing clinical trial management services to other organizations, employing CRAs to oversee and monitor trials on their behalf.

8. Independent consulting: Experienced CRAs may choose to work as independent consultants, offering their services to various organizations on a contract basis.

These organizations represent some of the main employers for Clinical Research Associates. Job seekers can explore job postings and career pages of these organizations to find suitable CRA job opportunities.

Clinical Research Associate  Jobs Salaries In Different Countries

Clinical Research Associate (CRA) salaries can vary significantly depending on factors such as experience, employer, location, and the cost of living in different countries. Here are approximate annual salary ranges for CRAs in several countries, based on industry data and salary surveys:

1. United States:

   - Entry-level CRA: $50,000 - $65,000

   - Experienced CRA: $65,000 - $95,000

   - Senior CRA: $95,000 - $130,000

2. United Kingdom:

   - Entry-level CRA: £25,000 - £35,000

   - Experienced CRA: £35,000 - £50,000

   - Senior CRA: £50,000 - £65,000

3. Canada:

   - Entry-level CRA: CAD 45,000 - CAD 60,000

   - Experienced CRA: CAD 60,000 - CAD 85,000

   - Senior CRA: CAD 85,000 - CAD 110,000

4. Australia:

   - Entry-level CRA: AUD 55,000 - AUD 70,000

   - Experienced CRA: AUD 70,000 - AUD 95,000

   - Senior CRA: AUD 95,000 - AUD 130,000

5. Germany:

   - Entry-level CRA: €40,000 - €50,000

   - Experienced CRA: €50,000 - €70,000

   - Senior CRA: €70,000 - €90,000

6. India:

   - Entry-level CRA: INR 300,000 - INR 500,000

   - Experienced CRA: INR 500,000 - INR 900,000

   - Senior CRA: INR 900,000 - INR 1,500,000 Please note that these figures are approximate and should be used as a general guideline. Actual salaries can vary based on factors such as company size, specific job responsibilities, and individual qualifications. It is recommended to research salaries for CRA positions in your target location and industry to get a better understanding of the current market rates.

CROs That Offer Clinical Research Associate   Jobs

Contract Research Organizations (CROs) are significant employers of Clinical Research Associates (CRAs). Many CROs operate globally and offer a wide range of clinical research services, including clinical trial management and monitoring. Some of the leading CROs that offer CRA jobs include:

1. IQVIA (formerly QuintilesIMS)

2. PPD (Pharmaceutical Product Development)

3. PRA Health Sciences

4. Syneos Health (formerly INC Research/inVentiv Health)

5. Covance (a part of LabCorp)

6. ICON plc

7. Parexel International

8. Medpace

9. Charles River Laboratories

10. Worldwide Clinical Trials

11. Premier Research

12. Celerion

13. Chiltern (now part of Covance)

14. Rho

15. CMIC Group

These are just a few examples of the numerous CROs that offer CRA job opportunities. It's important to keep in mind that the clinical research industry is dynamic, with new companies emerging and existing ones undergoing mergers and acquisitions. As a result, it's essential to stay updated on the latest industry trends and developments and explore the websites of these CROs to find the most current CRA job openings.

SAS Or Clinical Research Associate   Which One Is Better For Career

Choosing between a career as a Statistical Analysis System (SAS) programmer and a Clinical Research Associate (CRA) depends on your personal interests, aptitude, and long-term career goals. Both careers can be rewarding and offer growth opportunities, but they require different skill sets and responsibilities. Let's explore some key differences between the two roles to help you make an informed decision:

1. Job Responsibilities:

   - SAS Programmer: SAS programmers primarily work with statistical analysis software to process, analyze, and interpret clinical trial data. Their responsibilities include programming and validating statistical models, generating tables, listings, and figures, and ensuring data quality and compliance with regulatory guidelines.

   - CRA: CRAs are responsible for monitoring clinical trials, ensuring compliance with good clinical practice (GCP) guidelines, and overseeing the progress and data quality of clinical trials. They liaise with site personnel, manage site visits, and review documentation to ensure the safety and rights of trial participants are protected.

2. Skill Sets:

   - SAS Programmer: A strong background in statistics, programming, and data analysis is essential for this role. Proficiency in SAS software and familiarity with other programming languages, such as R or Python, is required. Attention to detail, problem-solving skills, and the ability to work independently are also crucial.

   - CRA: CRAs should have excellent organizational, communication, and interpersonal skills. They need to work effectively with diverse stakeholders, including investigators, site personnel, and sponsors. Attention to detail, adaptability, and a strong understanding of clinical research regulations and guidelines are necessary for success in this role.

3. Educational Background:

   - SAS Programmer: A bachelor's or master's degree in statistics, biostatistics, mathematics, data science, or a related field is typically required. Some employers may prefer candidates with a background in life sciences, such as biology or pharmacology.

   - CRA: A bachelor's degree in life sciences, nursing, pharmacy, or a related field is usually required. Some employers may prefer candidates with a master's degree or higher in a relevant discipline.

4. Work Environment:

   - SAS Programmer: SAS programmers typically work in an office setting with a structured schedule. They may collaborate with other team members, such as biostatisticians, data managers, and clinical trial coordinators.

   - CRA: CRAs often have a more flexible work environment, as their responsibilities involve site visits, which may require frequent travel. They interact with various stakeholders, including site personnel, investigators, and sponsors.

Ultimately, the decision between pursuing a career as a SAS programmer or a Clinical Research Associate depends on your interests and the type of work you enjoy. If you are passionate about statistical analysis, data management, and programming, a career as a SAS programmer may be more suitable. However, if you enjoy working with people, managing clinical trial sites, and ensuring compliance with regulations and guidelines, a CRA role might be a better fit. Both careers offer growth opportunities and competitive salaries, so carefully consider your long-term goals, interests, and skills when making your decision.

How I will Get Certification:

To get CRA certification you have to clear the ACRP, CCRC, CPI or ACRP-CP entrance.  Once you clear this exam you will be known as a professional CRA. We will give you 100% guarantee that you will clear this exam with the best percentage.

Course Reviews

  • Oliver P.
    Oliver P.
    1970-01-01
    Google

    The course was very comprehensive and covered all aspects of clinical research. The instructors were highly experienced and provided valuable insights into the industry. I feel much more confident in my ability to perform as a Clinical Research Associate after completing this course.

  • Nithya F.
    Nithya F.
    1970-01-01
    Google

    The course provided a great overview of the clinical trial process and the various stages involved. It gave me a clear understanding of the CRA's role in ensuring the integrity of the data and the safety of the trial participants.

  • Prudhvi A.
    Prudhvi A.
    1970-01-01
    Google

    I wish there had been more emphasis on the practical aspects of the CRA job, such as site visits and monitoring activities. While the course provided a good foundation in clinical research, I still feel like I need more hands-on experience to be confident in my role as a CRA.

  • Rama W.
    Rama W.
    1970-01-01
    Google

    The course content was well-organized and logically structured, which made it easy to follow along and understand complex topics. The course materials were well-written and easy to understand, even for someone without a background in clinical research.

This Course Features

Unlimited training Attempts

Pay once and get life-time training access

Daily Class Recordings

Get life-time access for daily class recordings along with training

24/7 support

Support available for 24/7

Resume and Interview Preparation

Help in resume and interview preparation along with training

Course Curriculum

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