You profile has been submitted for review.
Deepa Purohit Clinical Research, Clinical Data Management, SAS
No reviews yet
Headline: Expert Trainer in CDM, Clinical SAS, Regulatory Affairs & Medical Writing | ICH-GCP Specialist
Bio:
"Maximize your career potential in the global life sciences industry with expert-led, hourly coaching. I am a Senior Clinical Research Trainer specializing in the end-to-end clinical development process. I offer targeted training for international students and professionals in:
Clinical Data Management (CDM): Master the data life cycle, from CRF design to database lock, ensuring data integrity and quality.
Clinical SAS: Learn to program, analyze, and report clinical trial data using industry-standard SAS tools.
Regulatory Affairs: Deep dive into Global Regulatory Pathways (IND, NDA, ANDA) and compliance with FDA, EMA, and PMDA standards.
Medical Writing: Training on high-quality clinical study reports (CSRs), protocols, and investigator brochures.
Why Train With Me?
Industry Simulations: I don't just teach theory; I provide real-time industry insights through hands-on simulations of trial scenarios.
Regulatory Mastery: Comprehensive coaching on ICH Guidelines (GCP, E3, E6, E8, E9, M1, M4 and M8) to ensure you are ready for global audits.
Whether you are a graduate student or a professional transitioning into a new role, I provide flexible, hourly sessions tailored to your specific learning goals and time zone."
Bio:
"Maximize your career potential in the global life sciences industry with expert-led, hourly coaching. I am a Senior Clinical Research Trainer specializing in the end-to-end clinical development process. I offer targeted training for international students and professionals in:
Clinical Data Management (CDM): Master the data life cycle, from CRF design to database lock, ensuring data integrity and quality.
Clinical SAS: Learn to program, analyze, and report clinical trial data using industry-standard SAS tools.
Regulatory Affairs: Deep dive into Global Regulatory Pathways (IND, NDA, ANDA) and compliance with FDA, EMA, and PMDA standards.
Medical Writing: Training on high-quality clinical study reports (CSRs), protocols, and investigator brochures.
Why Train With Me?
Industry Simulations: I don't just teach theory; I provide real-time industry insights through hands-on simulations of trial scenarios.
Regulatory Mastery: Comprehensive coaching on ICH Guidelines (GCP, E3, E6, E8, E9, M1, M4 and M8) to ensure you are ready for global audits.
Whether you are a graduate student or a professional transitioning into a new role, I provide flexible, hourly sessions tailored to your specific learning goals and time zone."
Subjects
-
Clinical Research Beginner-Expert
-
Clinical SAS Beginner-Intermediate
-
Clinical Data Management Beginner-Expert
Experience
-
Training Manager (Apr, 2025–Present) at ProPharma Academy
Training students and working professionals in clinical trial operations, clinical data management, clinical SAS, medical writing and regulatory affairs. -
CDM & SAS trainer (Sep, 2024–Apr, 2025) at ' 02 year experience in Freelance tutoring
-
Research Associate (Nov, 2009–Jun, 2014) at Himalaya Wellness Company, Bangalore
As research Associate I was involved in Medical writing.
Education
-
Advanced Diploma in Clinical Research, Clinical Data Management and Clinical SAS (Mar, 2024–Sep, 2024) from Clinilaunch Research Institute, Banglore
-
Bachelor of Engineering (Oct, 2005–Jun, 2009) from Visvesvaraya Technological University, Belagavi
Fee details
₹800–2,000/hour (US$8.42–21.05/hour)
Charges vary based on content and the student's expertise level
-
-
Vellore, Tamil Nadu, India
-
Can travel:
No
-
- Last login: May 12
- Registered: Feb 21
- Total Teaching exp: 2.0 yrs.
- Teaches online: Yes
- Online Teaching exp: 2.0 yrs.
- Teaches at student's home: No
- Homework Help: No
-
Gender: Female
- Works as: Individual teacher
- Speaks: English, Hindi, Kannada, Tamil, Telugu
-
Fee:₹800–2,000/hour(USD 8.42–21.05/hour)
Reviews
No reviews yet. Be the first one to review this tutor.
