Turn Your Life Science Degree Into a High-Growth Clinical Research Career
India’s most practical & job-ready training in Clinical Research, made for students & freshers like you.
100% Placement Support | Faculty with 15+ Years Experience | Practical Training Included
Introducing the Advanced Diploma in Clinical Research (ADCR)
ADCR is a 12-month industry-backed clinical research training program designed for Life Science graduates and early professionals who want to confidently start their careers in global clinical trials & allied domains.
The course bridges the gap between academic theory and real-world clinical research processes , with a complete focus on employability, interview preparation, and role-based practical exposure.
Who Is This Course For?
▪️Science, Life Science, Pharma, Nursing, Allied‑health Grads (e.g. B.Sc., M.Sc., B.Pharm, M.Pharm, Pharm D, BHMS, BAMS, Nursing)
▪️Healthcare professionals aiming to transition into clinical research (e.g. Physiotherapists, Lab Technicians)
▪️Aspiring CRAs, CRCs, Data Managers, Pharmacovigilance & Regulatory specialists
What You'll Learn
🔍 Research Concepts in Simple Language
🗣️ Active Learning Techniques
📋 SIV (Site Initiation Visit) Mastery
📂 Solo Document Handling
🏥 Real-World Exposure
🎤 Interview & HR Readiness
✅ Professional Accountability
🚀 Job Market Navigation
Why Choose ADCR at Canvass?
Why Life Science Graduates Struggle
Even after completing BSc, MSc, B.Pharm, Pharm D, or Nursing, most students find themselves lost when applying for clinical research roles. Here’s why:
▪️Only Theory, No Real Exposure
▪️Confusing, Jargon-Heavy Modules
▪️No Guidance for Job Interviews & Orgnizations
▪️No Clarity on job Roles & Pathways
▪️Zero Support After Course Completion
Here’s how Canvass Academy’s ADCR Course Solves It
ADCR is built to fix all of the above — with practical, guided, career-oriented training.
🎓 Layman-Friendly Curriculum
📂 Training on process, softwares & documents
🧑🏫 Experienced Faculties
💼 Job-Readiness Coaching
✅ Real Project Visits
📹 Cameras, Viva & Accountability
Upcoming Free Webinar
First Job Success – 5 Evidence-Based Steps to Nail Your Application
🗓️ 19 July | ⏰ 6 PM to 8 PM 🎙️ Moderator: Vijaya Bhakte
Know Your Speakers
Navneet Kaur Sehgal/ Menka Aahuja
Expert in Graphology, English Language, and Personality Development Training. Specializes in preparing students for one-on-one interviews.
Conducted Personality Development sessions for B. Pharm and Life Science students, equipping them with interview skills and communication techniques.
Delivered Graphology workshops to over 1,000 students, helping them understand handwriting analysis and its role in personal growth.
Why Many Life Science Graduates Miss Out on Clinical Research Jobs
🗓️ 25 July | ⏰ 6 PM to 8 PM 🎙️ Moderator: Vijaya Bhakte
Know Your Speakers
Dr. Anupama Hariharan
Associate Director at IQVIA Biotechnology, leading a team of project managers across Australia, New Zealand, Southeast Asia, and South Korea; HBA Ambassador, and APAC Mentor.
Education: BDS, MSc Clinical Research
Want to know if this course is for you?
Advanced Diploma in Clinical Research
Unlock Your Potential in Clinical Research & Allied Domains!
Join our comprehensive training program and become a vital part of cutting‑edge healthcare research.
Why Choose This Program?
Strategic Career Pathways
India’s evolving clinical research sector offers robust growth across roles like CRC, Data analyst, BA/BE CRA, Pharmacovigilance Associate, & Regulatory Affairs Specalist.
Clear Progression
From junior coordinator to senior CRA or Project Manager—with structured development and certifications guiding your journey.
Hands-On Training
Learn Good Clinical Practice, trial design, data management, protocol , SOP, monitoring, patient safety, and regulatory frameworks for India & other countries
Real-World Exposure
Simulated and live projects with CROs and pharma sponsors offer practical insight and international standards
Career Resilience & Stability
Diverse opportunities in global companies ensure job continuity, even if a project ends
Program Highlights
GCP, ethics, patient safety, trial monitoring, and documentation
GCP, ethics, patient safety, trial monitoring, and documentation
Data Management
CDM principles, EDC platforms, CDISC standards
Specialist Tracks
Clinical Operations, Pharmacovigilance, CDM, Regulatory Affair, eTMF, Medical Writing
Soft Skills
Leadership, communication, teamwork, cross-functional collaboration