Join the Best Clinical Research Courses in Pune at India's Top Rating Training Institute, and Learn Clinical Data Management, Pharmacovigilance, Drug Development, Monitoring of Trial, Regulatory Affairs & Etc.
Job-Oriented Training | 3 Months | 5 Days/Week 100% Placement Assistance | Online / Offline / Self-Paced
3 Months Duration
5 Days / Week
100% Placement Assistance
Online & Offline Training
PCRTI offers a career-focused Clinical Research Course in Pune. It is designed to help graduates and working professionals build job-ready skills for the clinical research and drug development industry. The program is structured for practical learning, strong fundamentals, and real-world workflow understanding. This helps you prepare to learn effectively and perform confidently in interviews and entry-level roles.
This diploma course in Pune covers the full clinical research ecosystem. It includes Clinical Research, Trial Monitoring, Clinical Data Management (CDM), Pharmacovigilance (PV), Regulatory Affairs (RA), ICH-GCP (E6), Drug Development, and Protocol Designing. The course includes expert-led sessions, case-based learning, weekly assessments, presentations, mock interviews, and placement support. PCRTI helps you move from “beginner” to “job-ready” in a focused timeframe.
Join PCRTI to get expert training and build a successful career in the expanding field of clinical research.
3 Months
5 Days/Week + Quizzes
Concept + Workflow
ICH-GCP, CDM, PV, RA
Interviews & Resume
Life Science, Medical
Ready to start? Join PCRTI to build a successful career.
Understand the field, its importance, and your potential growth.
Clinical research is a branch of healthcare science that studies the safety and effectiveness of medicines, medical devices, treatments, and diagnostic methods. It ensures that new medical advancements are tested thoroughly before they are introduced to the public.
This field includes clinical trials, observational studies, and other research methodologies that help improve patient care and healthcare outcomes. By evaluating new drugs and therapies, clinical research plays a critical role in advancing medical knowledge and addressing unmet medical needs globally.
Clinical research connects medical innovation to patient care by proving if new treatments are safe and effective. It ensures side effects are tracked, data is reliable, and patient rights are protected throughout the study. This critical process drives companies to hire professionals who have mastered documentation, GCP compliance, monitoring workflows, and safety reporting.
Clinical research offers promising career opportunities in India and globally, with increasing demand for trained professionals across CROs, hospitals, and research organizations. India’s clinical research ecosystem continues to grow, creating opportunities across trial operations, safety, data, and regulatory functions.
As a career path, clinical research is expanding because it provides multiple specializations (CRA/Monitoring, CDM, PV, RA, Medical Writing), growth potential with experience and trial exposure, and opportunities in India as well as international markets (role-dependent).
If you want a career that combines healthcare knowledge with structured processes, documentation, compliance, and teamwork, clinical research is a strong long-term option.
Our Clinical Research course is suitable for graduates and professionals from Life Science, Pharmacy, Nursing, and Healthcare backgrounds who want to build a career in the clinical research industry.
Our course focuses on practical, job-relevant skills required in real clinical research roles. By the end of the course, you can expertly navigate protocol execution, regulatory compliance, and ICH-GCP ethical standards.
You will build technical proficiency in clinical monitoring workflows, data management (CDM) quality control, and pharmacovigilance (PV) safety reporting. Beyond technical theory, we secure your professional career with intensive interview preparation, including mock drills and presentation practice, to make you industry-ready from day one.
Shivani S.
Medical QA
Package : 3.5 LPA
Mayuri W.
Medical QA
Package : 3.5 LPA
Pranav Y.
Pharmacovigilance
Package : 3.5 LPA
Abhimanyu U.
Pharmacovigilance
Package : 3.5 LPA
Dhanashri N.
Pharmacovigilance
Package : 3.5 LPA
Bhagyashree J.
Pharmacovigilance
Package : 3.48 LPA
Sakshi N.
Pharmacovigilance
Package : 3.48 LPA
Mohini P.
Pharmacovigilance
Package : 3.48 LPA
.webp){kind=logo}
The Clinical Research course duration is 3 months with 5 days/week structured learning. This format helps you build consistency and confidence through continuous practice - ideal for freshers as well as working professionals seeking career transition.
Our course is designed to provide comprehensive training in the field of clinical research, covering all aspects from basic principles to advanced techniques.
Build fundamentals, understand terminology and why clinical research matters, and how India fits into global clinical trials.
Start your journey with a comprehensive Introduction to Clinical Research, master key Terminologies in Clinical Research, explore the strategic Advantages of CR in India, and solidify your knowledge with dedicated Notes and Quizzes.
Understand the complete drug development journey and how clinical research fits into it.
Gain a complete Overview of Drug Development, navigate through the distinct Clinical Trial Phases, master the basics of BA/BE Studies, and reinforce your expertise with comprehensive Notes and Quizzes.
Learn how trial data is captured, validated, cleaned, and made reliable for outcomes and submissions.
Explore the core pillars of data integrity including CFR Part 11 basics, the fundamentals of CRF Design, and a comprehensive Introduction to CDM. This module equips you with essential skills in Data Entry Methods, precise Query Management, and Source Data Validation, while preparing you for the industry's evolution with insights into the Future of Data Management.
Learn the ethical and scientific backbone of clinical trials to protect subjects and ensure data integrity.
Trace the History of international regulations, master the standards of Good Clinical Practices, and understand the role of the Ethics Committee, while defining Investigator Responsibilities, Sponsor Responsibilities, the Protocol & Investigator Brochure, and the management of Essential Documents.
Understand drug safety monitoring during and after trials and safety documentation mindset.
Master the critical processes of Adverse Event Reporting, the accurate Recording of Event, and the Medical Management of Adverse Events, while gaining conceptual insights into Handling Death, Unblinding of Drug, Clinical Safety & Pharmacovigilance, and the Naranjo Assessment concept.
Understand regulatory basics and compliance requirements in clinical research environments.
Navigate the regulatory framework by understanding the concepts behind the Application of Permission and Approval of Clinical Trials, while mastering CFR basics, high-level CT Rules, and the ICMR guidelines overview, alongside an introduction to Medical Devices and Guidelines for Industry.
Gain understanding of monitoring flow, site visits, IP management basics, and audit readiness.
Navigate the critical oversight mechanisms of Audits and Inspections, understand the operational Flow of Events, and master Investigational Drug Management, while learning the practical execution of Routine Monitoring Visits and the comprehensive Site Visit Flow.
Learn how protocols are structured and how to think in terms of study design and ethics.
Learn to draft a study protocol, master the intricacies of Study Design, ensure ethical compliance through Informed Consent, and solidify your understanding with structured Notes and Quizzes.
PCRTI focuses on structured training + interview readiness + career support, making learning practical and aligned to entry-level job expectations.
Process + Expectations
Attendance + Assessments
CRA/CTC/CDM/PV aligned
HR + Technical rounds
Application strategy
Openings & eligibility
Improve after interviews
First weeks guidance
Understand the complete trial lifecycle, learn the basics of ICH-GCP ethics, and develop a strong eye for detailed documentation. Build essential communication skills, master the fundamentals of Clinical Data Management and Pharmacovigilance safety workflows, and grow your career with consistency, a learning attitude, and professionalism.
After course completion, candidates can apply for entry-level and mid-level roles in India and abroad (role availability depends on hiring needs and profile strength).
Salary varies by role, company, and trial exposure, but typical ranges are:
How You Become Job-Ready
Career goal mapping & track selection
Trial flow + terminology basics
GCP, Monitoring, CDM, PV, RA, Protocol
Weekly quizzes + case studies
Communication + confidence practice
Technical + HR rounds
Professional profile guidance
Assistance & support
Take the first step towards a successful Clinical Research career. Join PCRTI and unlock your potential with hands-on training, expert mentorship, and guaranteed placement support. Your future in Clinical Research starts here!
100% Placement Assistance
15+ʸʳ Expert Trainers
200+ Hiring Partners
Unlimited Interview Calls
Pay in Installments Options
Weekly Assessments
Interview Preparation
Pricing Best and Affordable
Sessions Doubt Clearing
Detailed Curriculum
Upon successful completion of the Clinical Research Course, you will receive a prestigious certificate from PCRTI. This certificate:
Clinical Research
"Excellent Learning Experience! PCRTI Systems offers has top notch clinical research courses... The trainers are very knowledgeable and make even hardest topics easy to understand. The course is very detailed and up to date. Highly recommended course"
Clinical Research
"PCRTI’s clinical research course is worth every ruppee. The trainers are professional and always ready to help. They made difficult topics easy to learn, and the placement team was extremely supportive throughout my job search."
Clinical Research
"Best clinical research training institute in Pune, I have completed my clinical research course here and also got placement at Fortrea. I really recommend for clinical research courses in Pune."
Clinical Research
"I had a great experience with PCRTI’s Clinical Research Course in Pune. The trainers explained every concept in a very simple and practical way, which helped me gain confidence. Thanks to the dedicated placement team, I was able to secure a job quickly after completing the course. Highly recommended for anyone looking to build a career in Clinical Research!"
