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Get Brochure to Your MailWelcome to Clin Infotech Pharmacovigilance Internship Program!
Clin Infotech is offering Pharmacovigilance Internship Program we are confined to provide Practical Training in Clinical Research & Pharmacovigilance with hands-on Practical Experience on Oracle Argus Safety Database by Industry Experts.
Pharmacovigilance is the science and activities relating to the detection, assessment, understanding and prevention of adverse effects or any other medicine/vaccine related problem. All medicines and vaccines undergo rigorous testing for safety and efficacy through clinical trials before they are authorized for use. The Pharmacovigilance Operations Intern will assist in the receipt, processing, reporting, and management of Individual Case Safety Reports (ICSRs) in compliance with applicable regulation, the company's Standard Operating Procedures, and project-specific operational agreements. With the increasing demand for Pharmacovigilance professionals, gaining hands-on experience through an internship is crucial to kick start your career in Pharmacovigilance.
Pharmacovigilance Internship at Clin Infotech:
Our Pharmacovigilance Internship Program is designed to provide aspiring Pharma Professionals with practical experience in working on real-world projects. This internship aims to bridge the gap between theoretical knowledge and practical application by immersing you in hands-on projects under the guidance of industry experts.
Pharmacovigilance Internship Program Overview
The internship program covers a wide range of topics, including Case Processing, Case quality check, PUSR and Its Submission Timelines, MEDDRA Coding, Clinical Development Process, SAE Narrative Writing and Duplicate Check and Case initiation. You will also gain exposure to popular tools and technologies used in the industry, such as Oracle Argus, MedDRA Coding and WHO DD Coding.
About the Program:
Our Pharmacovigilance Internship Program offers a comprehensive curriculum that is structured to provide a step-by-step learning path. You will receive guidance and mentorship from experienced industry professionals who will assist you throughout the internship, ensuring a seamless learning experience.
Modules Covered
Module 01: Introduction to Pharmacovigilance
Module 02: Pharmacovigilance regulations and regulatory authorities
Module 03: ICH Guidelines, GVP Modules for Pharmacovigilance
Module 04: Adverse Event Reporting forms (CIOMS, Yellow card, Med Watch)
Module 05: Drug safety evaluation in special population
Module 06: Entries related to Pharmacovigilance reporting databases (ARGUS)
Module 07: Adverse events (AEs) and Adverse drug reactions (ADRs)
Module 08: Causality or causal relationship determination
Module 09: Dechallenge and Recalling
Module 10: Drug exposure during pregnancy and breastfeeding
Module 11: Narrative formats for various case reports
Module 12: Spontaneous, Literature and Study reports
Module 13: Valid and invalid reports
Module 14: Assignment and case studies
Pharmacovigilance Internship Program Outcomes
Why Take This Pharmacovigilance Internship Program?
There are several reasons why you should consider enrolling in our Free Data Science Internship Program:
Practical Experience: The internship offers hands-on experience working on real-world projects, which is invaluable in the field of IT MNC Companies.
Mentorship from Industry Experts: You will receive guidance and mentorship from experienced professionals who will share their knowledge and insights to help you succeed.
Industry-Relevant Curriculum: Our curriculum is designed to equip you with the skills and knowledge that are in high demand in the Pharmacovigilance industry.
Interactive Lectures: Engage in live lectures conducted by industry experts, where you can ask questions and interact with fellow interns.
Hands-on Projects: Apply your learning to real-world projects and gain practical experience working with Pharmacovigilance from IT domains.
Assignments and Assessments: Complete assignments and assessments to reinforce your understanding of concepts and measure your progress.
Capstone Project: Conclude your internship by working on a comprehensive capstone project that showcases your skills and knowledge.
Why CLIN INFOTECH?
- Clin Infotech is a leading training institute in the field of Advance Clinical Research Training Program. Here's why you should choose us:
- Industry-Experienced Faculty: Our instructors are seasoned professionals with extensive industry experience, ensuring that you receive practical insights and real-world perspectives.
- Hands-on Approach: We emphasize a hands-on learning approach, enabling you to apply theoretical concepts to practical scenarios.
- 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.
- Job Placement Assistance: We provide comprehensive job placement assistance to help you secure lucrative career opportunities in the IT industry.
- Our Alumni Work At:
- 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:
- Complete Course Material will be provided including detailed information about the entire workflow of a Clinical Research Associate.
- 2 months internship available after rigorous training in Medical Writing.
- Own CRO live projects.
- Highest placement record across all training institutes.
- Industry-based SOPs training.
- Trainers with a minimum of 7+ years of experience.
- Comprehensive teaching by medical doctors.
- 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:
- Resume Preparation
- Interview Preparation with real-time questions and answers
- Mock Interview Sessions
- Communication Skills and Personality Development Sessions
- Placement Assistance
- 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.