Clinical Research Associate Training – CRA Training Program

Advance your Career through Clinical Research Associate Training Program (CRA Training Program) through Clinical Research Associate course Curriculum enveloping fundamental themes like Clinical Trials, Drug Development Process and Clinical Trial Management System, Protocol Guidelines Etc.., .Our Job Oriented  Interactive-CRA Training program for Clinical Research Professionals are intended for people with or without earlier clinical trial experience, make to be successfully can get job as a Principal Investigator (PI), Clinical Research Associate (CRA), Clinical Research Coordinator (CRC), Clinical Data Coordinator or Clinical Data Manager (CDM). The CRA Training Program at Clin Infotech not only make to get job but we make to gain complete Practical Knowledge in the Clinical Trial Management System.

This Clinical Research Associate course includes classroom sessions with industry experts and Clinical Research professionals from the field of Clinical Trials, gives live Session about the Clinical Trial process, CRF Designing,Process,Clinical Trial Management, Clinical Trial Phases, process involved in the Clinical trial Phases and the roles and responsibilities of clinical research Associate.Experts carefully design this course with methods proven to give results and give the students amazing learning experience.The Candidates with Pharmacy, Life Sciences, BDS Dental, Medical and Nursing Graduates can Participate in CRA Training and Placement Program. They can also join in CRA Online training program or CRA Class room training program.

CRA Course Curriculum:

Module 1: Drug Development Process, Good Clinical Practice (GCP), and Clinical Research Team Roles and Responsibilities

Module 2: IRB, Clinical Study Protocol Elements and Amendments

Module 3: Informed Consent

Module 4: Investigational Product Accountability

Module 5: Safety Definitions and Reporting Requirements

Module 6: Source Document Verification

Module 7: Monitoring the Study

Module 8 and Module 9: Monitoring Visit Reports and Contact Reports

Module 10: Regulatory Compliance and Quality Assurance: Audits and Inspections

Why One Should Take The Clinical Research Associate Course?

Is Clinical Research Associate certification being worth pursuing as a career?

The answer is a big YES for myriad reasons. The Clinical Trials for Different Drugs has been Increasing because of the growing Clinical Trials the demand for the Clinical research Professionals has been increasing who has completed Clinical Research Associate training and placement Program with Certification. The Clinical Research domains is creating tons of Clinical Trial data and the demand for the Clinical Research professionals who can evaluate and extract meaningful insights is increasing and creating millions of clinical research jobs.

• 1.4 Lakh Clinical research Associate Job Opportunities are available
• The world will notice a deficit of 2.3 Lakh Clinical Research professionals by 2021
• The Demand for Clinical Research professionals has increased by 417% in the year 2018, in India, as per the Talent Supply Index

What does a Clinical Research Associate do?

Clinical Research Associate Job Description:

• As a Clinical Research Associate (CRA) you will be responsible for setting up, coordinating and supervising clinical studies (trials) with medicines, medical nutrition or medical devices. You will be  doing the  selection, initiation, monitoring and close-out visits at the participating clinical trial centers. During a monitor visit you will verify various (patient) data included in the eCRF (electronic Case Report Form) by the physician-researcher (investigator, medical specialist) or research nurse. This process, called source data verification (source being the electronic patient file, EPD) checks whether the study has been carried out in accordance with applicable laws and regulations (Good Clinical Practice, ICH-GCP) and company Standard Operating Procedures (SOP’s).
• Develop and write trial protocols (outlining purpose and methodology.
• present trial protocols to a steering committee
• design data collection forms, known as case report forms (CRFs)
• Coordinate with the ethics committee, which safeguards the rights, safety and wellbeing of all trial subjects.
• Manage regulatory authority applications and approvals that oversee the research and marketing of new and existing drugs
• identify and assess the suitability of facilities to use as the clinical trial site
• identify/select an investigator who will be responsible for conducting the trial at the trial site
• liaise with doctors, consultants or investigators on conducting the trial
• set up the trial sites – ensuring each centre has the trial materials, including the trial drug often known as the investigational medicinal product (IMP)
• train the site staff to trial-specific industry standards
• monitor the trial throughout its duration, which involves visiting the trial sites on a regular basis
• verify that data entered on to the CRFs is consistent with patient clinical notes, known as source data/document verification (SDV)
• collect completed CRFs from hospitals and general practices
• write visit reports and file and collate trial documentation and reports
• ensure all unused trial supplies are accounted for
• close down trial sites on completion of the trial
• discuss results with a medical statistician, who writes technical trial reports
• archive study documentation and correspondence
• prepare final reports and occasionally manuscripts for publication.
• The objective of a clinical drug study is to demonstrate that the investigational product has a certain desired effect for the disease or disorder for which it is being developed, whether it is safe, and that all adverse reactions / adverse events have been reported according to the study protocol and have been rated on seriousness, severity, and causality with the investigational product. Clinical studies are classified according to their phase in development:

Job Opportunities With Clinical Research Associate Clinical

Clinical Research Associate Salary?

Clinical researches Associate Salary are in the region of 2.4 Lakhs to 4.5 Lakhs. It’s likely these posts will require some experience in a related area along with the CRA certification Program from Reputed CRA training institutes in Hyderabad.

Eligibility

Any Graduate/ B.tech/ B.Sc. in Microbiology/ Life Sciences/ Botany/ Zoology/ Food Science/ Food Technology/ BE/ B.Pharma/ MBBS/ BDS/ BHS/ BUMS/ BAMS or any other discipline. Diploma holders are eligible for our Clinical Research Associate Certification and CRA training and Placement Program

Registration

The Candidates Can Register at Clin Infotech through our Register Link or contact our Management Team. They can Register for Clinical Research Associate Online program or class room program. The CRA Online program will be provided with the LMS Access.The registration dates for Clinical Research Associate Training program. The Effective E-learning tools incorporated into the design of the webpage make the CRA course lectures, online live classes and study material easily accessible.

Clinical Research Associate Companies:

IQVIA,Covance,Parexel,Asiatic clinical Research,Astron research,BioAxis,Bioclinica,Axis Clinical,Croissance,Dubar Research foundation,eresearch technologies,global clinical Trials,GVK Biosciences,Kemwell Biopharma,labcorp,Lambda Therapeutics,Makro care,Navitas LifeSciences,Novotech,PPD,Sai Life Sciences,Spectrum Clinical Research,Strides Pharma Research,symphony,syneos Health Care,Syngene,Techobserver,Vedic  Life sciences Etc.

Interview Preparation Sessions

Participants who have completed the Clinical Research Associate course training will be put under our Placement Incubation Program. As part of this program, participants will undergo a thorough CRA interview preparation process. A huge repository of  will be provided for the participants to prepare after CRA online Certification. A dedicated Clinical Research Associate Trainee Expert (SME) will help in resume building, conduct mock interviews and evaluate each participant’s knowledge, expertise and provide feedback. Clinical Research Associate Resume Samples will be given and the participant should Update With Clinical Research Associate Skills. Our SMEs will do the necessary handholding on Clinical Research Associate interview preparation process till the time the participant is placed in Clinical Research Companies in Hyderabad, Pune Mumbai and Bangalore etc. Guidance is also provided on LinkedIn profile building and tricks of the trade to improve the marketability of the resume. – Clin Infotech Management.

Why CLIN INFOTECH?

1. Clin Infotech is a leading training institute in the field of Advance Clinical Research Training Program. Here's why you should choose us:
2. Industry-Experienced Faculty: Our instructors are seasoned professionals with extensive industry experience, ensuring that you receive practical insights and real-world perspectives.
3. Hands-on Approach: We emphasize a hands-on learning approach, enabling you to apply theoretical concepts to practical scenarios.
4. Customized Learning Paths: Our programs are designed to cater to learners of various backgrounds and skill levels, allowing you to learn at your own space.
5. Job Placement Assistance: We provide comprehensive job placement assistance to help you secure lucrative career opportunities in the IT industry.
6. Our Alumni Work At:
7. Our alumni have successfully secured positions in leading organizations. Their achievements reflect the quality of our training programs and the practical skills they gained during their time with us.

Eligibility:

Minimum Eligibility Criteria For Application To The Course Would Be Either Of The Following:

Applicants are recommended to have one of the following life Science degrees: Bachelor’s, Master’s, or PhD, MBBS/ MD/B.D.S /M.D.S/ B.A.M.S / B.H.M.S /B.P.T/ B.Tech (Biotechnology / Pharmaceutical Science) / M.Tech (Biotechnology), B. Pharm /M.Pharm /BVSC / B.Sc. (Nursing) and all professionals working with Pharmaceutical companies, CROs and Hospital.

Admission Process:

The admission process for the Medical Writing Course with 100% placement assistance is very simple. Candidates can apply online through our website. After examining your application our executives contact you to complete the further procedure.

At Clin Infotech Systems, we are committed to assisting you every step of the way with our user-friendly online application process and committed admission officers. Prepare yourself to begin a fulfilling career in Medical Writing with our thorough admissions procedure.

Step 1: Apply Online at https://www.clininfotech.com

Step 2: Review the Application

Step 3: Contact and Further Process

Step 4: Enrolment and Confirmation

Step 5: Course Completion

Step 6: Assessments and Assignments

Step 7: Mock Test and Mock Interview

Step 8: Resume Preparation

Step 9: Skill Development

Step 10: Placement Assistance

Trainers and Training Process

At Clin Infotech, we have the best faculties with 15+ years of real-time experience in the clinical research industry. The course curriculum is specially developed with respect to the current industry trends and standards. Students will have the access to our online sessions. Additionally, the students will get a chance to clear their doubts on alternate weekends. Also, the practice interview sessions are also conducted by our trainers followed by timely assessments.

The trainers will help our students to pass their interviews smoothly and get placed in a good company.

Clin Infotech advantage:

1. Complete Course Material will be provided including detailed information about the entire workflow of a Clinical Research Associate.
2. 2 months internship available after rigorous training in Medical Writing.
3. Own CRO live projects.
4. Highest placement record across all training institutes.
5. Industry-based SOPs training.
6. Trainers with a minimum of 7+ years of experience.
7. Comprehensive teaching by medical doctors.
8. Hands-on training will be provided on clinical research sites.

Our team of experienced drug safety specialists also provides the following services upon successful completion of the training:

1. Resume Preparation
2. Interview Preparation with real-time questions and answers
3. Mock Interview Sessions
4. Communication Skills and Personality Development Sessions
5. Placement Assistance
6. Placement Assurance

It's time to comprehend and put standard trail management ideas into practice in order to build a solid methodology for the evaluation and boost the timely completion of crucial trials for the benefit of patients. To plan, produce, monitor, and complete all project duties, you must acquire specific skills and knowledge.

Through its comprehensive certification program, Clin Infotech offers thorough instruction in clinical research throughout the whole clinical trial process. With the help of this clinical trial management course, instructors will make sure that students have a procedural and administrative understanding of the clinical trial process as well as the capacity to advance their knowledge and abilities.

This curriculum will teach you the whole Regulatory responsibilities involved in Document Creation; Planning, Organizing, Monitoring, Recording, Analysis, and Reporting of Human Clinical Trials, as well as the most recent discoveries and specialties in e-Clinical Technology.

Enroll Now!!

Certification:

• Certificate will be provided for this Course on successful completion of Assignments & Projects.
• Certificate would be awarded at the end of the program by Gratisol Labs. A fast track weekend course will also be conducted for employees & aspirants of Clinical Research Industry.

For more information, please contact Clin Infotech at careers@clininfotech.com or 8374457387

Ready to Apply For a Job Immediately After Your Internship

Clinical Research Associate Course Qualification?

• Clinical Research Associates with less than two years of experience – in-house or field-based
• Those currently working in the industry in a different role and seeking to change roles
• The course is also ideal for “on-boarding” of individual new hires or entire teams (individual registrations required).

Why Clin Infotech The Clinical Research Associate Training Institute In Hyderabad?

Clin Infotech offers the best CRA Certification online Program along with classroom and self-paced e-learning certification courses. The complete CRA course details can be found in our course agenda on this page. We will provide the CRA Classes with Live Scenarios with the CRA trainer to make them understand the Clinical research Associate Roles and Responsibilities and that’s the reason Clin Infotech consider as the best CRA Institute in Hyderabad.

Clinical Research Associate Certification Process:

• All learning Participants will be led Assessment & CRA Online Certification Exam.
• All the participants are expected to appear for CRA online assessment
• After successful completion the participants will be certified as professional in Clinical Research Associate by Clin Infotech.

Placement Assistance & Corporate Relations

In recent months the Institute has witnessed more and more participation from professionals working with global pharmaceutical, healthcare and food giants like Dr. Reddy’s Laboratories, Aurobindo Pharma, Glenmark Generics, Cipla, Wockhardt, Pfizer, Abbott, Medtronic, Foster Corporation, IPCA Laboratories, Calyx, Mother Dairy, Bliss GVS Pharma, Al Rawabi, Almarai, Green Pastures, SeQuent, PepsiCo India, Mankind, Beryl Drugs, Allergy Therapeutics, CFTRI, Ciron, Sun Pharmaceutical, Novartis, GlaxoSmithKline, Ranbaxy , Biocon etc.

Clin Infotech Placement Resource Division actively recommends our students and training participants for various job requirements and specialized roles to Human Resource, Talent Acquisition as well as the heads of various departments in Pharmaceutical, Healthcare and Food industries on regular basis.

What is Clinical Research Associate?

• As a clinical research associate (CRA), you’ll run clinical trials to test drugs for their effectiveness, risks and benefits to ensure that they are safe to allow on to the market. They will work on new and existing drugs and will usually be employed by either a pharmaceutical company or a contract research organisation (CRO) with the Clinical Research Associate Skills which works on behalf of pharmaceutical companies. The professionals who perform these activities are said to be a Clinical Research Associate/ Clinical Researcher professional. Clinical Research is the most high-in-demand profession.

What are Clinical research Associate Salary?

• The Salary will be ranging from 2.4 Lakhs to 6.5 Lakhs Per anum.

What are the roles and responbilities of Clinical research Associate?

As a Clinical Research Associate (CRA) you will be responsible for setting up, coordinating and supervising clinical studies (trials) with medicines, medical nutrition or medical devices. You will be doing the selection, initiation, monitoring and close-out visits at the participating clinical trial centers. During a monitor visit you will verify various (patient) data included in the eCRF (electronic Case Report Form) by the physician-researcher (investigator, medical specialist) or research nurse. This process, called source data verification (source being the electronic patient file, EPD) checks whether the study has been carried out in accordance with applicable laws and regulations (Good Clinical Practice, ICH-GCP) and company Standard Operating Procedures (SOP’s).

What is the Clinical Certification Process?

• Clin Infotech offering Clinical Research Associate Training program and class room training. Whoever completed the CRA online certification has to undergo the assessment exam and should clear the exam to gain the clinical research associate certification.

Which is the Best Clinical Research Institute for CRA Course?

• Clin Infotech offering Best CRA course Or Clinical Research Associate Training program both Online and class room training With the Placement Offers Who ever completed the CRA certification course has to undergo the assessment exam and should clear the exam to gain the clinical research associate certification.