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Courses

Discover our wide range of medical courses and healthcare training programs designed to provide academic excellence, practical skills, and industry-relevant knowledge. Our expert-led programs prepare you for a successful career in nursing, paramedical sciences, and other healthcare fields.

Advance pg in CR with AI
Clinical research institute

Advance PG in Clinical Research with AI

A future-ready clinical research program integrating Artificial Intelligence to meet evolving industry demands in drug development, trial design, data management, and regulatory affairs.

Key Highlights

  • Clinical Trial Design & Phases

  • ICH-GCP & Regulatory Affairs (DCGI, FDA, EMA)

  • Site Management & Monitoring

  • Pharmacovigilance & Medical Writing

  • Biostatistics & Clinical Data Management

  • Artificial Intelligence in Clinical Trials

  • Predictive Modeling & Data Analysis using AI

  • Ethics & Compliance in AI-Driven Research

Eligibility

  • Graduates in Life Sciences

  • Pharmacy

  • Medicine (MBBS, BDS, BAMS, BHMS)

  • Nursing

  • Biotechnology

  • Biochemistry or Allied Health Sciences.

Career

  • Clinical Research Associate (CRA)

  • Clinical Data Analyst / AI Data Scientist

  • Pharmacovigilance Officer

  • Digital Clinical Trial Manager

  • Quality & Compliance Specialist

Course Duration: 

1 Year Course + Internship

Diploma in medical coding
Advance PG in clinical research with AI

Gain expertise in translating diagnostics, procedures, and treatments into standardized codes (ICD-10, CPT, HCPCS) crucial for billing, insurance claims, and health record management. Ideal for life sciences, pharmacy, and allied graduates

Key Highlights

  • Medical Terminology & Anatomy

  • ICD-10, CPT & HCPCS Coding Systems

  • Reimbursement & Claims Processing

  • Healthcare Documentation & Compliance

  • Ethics, Data Privacy & Auditing Practices

Eligibility

  • Open to graduates in Life Sciences

  • Pharmacy

  • Medicine

  • Nursing

  • Biotechnology

  • related fields.

Career

  • Entry-Level Coder: ₹2–5 LPA

  • Senior Coder/Auditor/Quality Analyst: ₹3.5–9 LPA+ pharmaaffairshub.comCareerInPharma

  • Employers include hospitals, insurance firms, BPOs, health IT and outsourcing providers, with remote and freelance roles on the rise.

Course Duration: 

6 Months Course + Internship

Crash Courses for 12th +
Diploma in medical coding

​Intensive training designed for students immediately after 12th grade. This crash course covers the essentials of Clinical Research, Pharmacovigilance, and Clinical Data Management, helping students gain foundational knowledge and industry-ready skills in a short period.

Key Highlights

  • Introduction to Clinical Trials: Study phases, regulatory guidelines, and protocol design.

  • Pharmacovigilance: Adverse event reporting, drug safety, and risk management.

  • Clinical Data Management: Data collection, validation, and integrity using industry-standard tools.

  • Interactive case studies, written assessments, and mock interview preparation included.

Eligibility

  • Graduates in Life Sciences

  • Pharmacy

  • Medicine (MBBS, BDS, BAMS, BHMS)

  • Nursing

  • Biotechnology

  • Biochemistry or Allied Health Sciences.

Career

  • Clinical Research Associate (CRA)

  • Clinical Data Analyst / AI Data Scientist

  • Pharmacovigilance Officer

  • Digital Clinical Trial Manager

  • Quality & Compliance Specialist

Course Duration: 

3 Months Course + Internship

Diploma QA / QC in clinical rrresearch
crash courses for 12th+ students

Develop expertise in QA / QC tailored for clinical research. This diploma ensures adherence to global regulatory standards, integrates audit methodologies, and strengthens compliance across clinical trial operations—covering key principles, processes, and tools essential for quality-driven research

Key Highlights

  • Fundamentals of Quality Management Systems (QMS, QA vs. QC)

  • Standard Operating Procedures (SOPs), QA Plans & QC Tools

  • Audit Training: Internal audits, retrospective data/system audits, inspection readiness

  • Site Management Metrics & Process Mapping (including PV, CDM, operations)

  • Regulatory Frameworks: FDA, EMA, DCGI inspection norms & Institutional Ethics Committees

Eligibility

  • Open to graduates and professionals from life sciences

  • pharmacy

  • biotechnology

  • medicine (MBBS, BDS, BAMS, BHMS)

  • allied health fields.

Career

  • QA/QC Associate in Clinical Research Organizations (CROs)

  • Clinical Trial Auditor

  • Compliance & Quality Specialist

  • Post-Marketing Surveillance Analyst

  • Quality Monitoring & Regulatory Inspectors

Course Duration: 

3 Months Course 

Diploma SAS CLINICAL RESEARCH
diploma QA/QC in clinical research

The Diploma in SAS in Clinical Research program is the bridges the gap between clinical data management and statistical analysis, preparing learners for high-paying roles in global drug development.

Key Highlights

  • Introduction to Clinical Research & SAS – Understanding clinical trial data flow and SAS applications in the healthcare domain.

  • SAS Programming Basics – Data sets, variables, libraries, and data import/export.

  • Data Management in SAS – Data cleaning, validation, and preparation for statistical analysis.

  • Hands-On Projects – Real-world datasets and clinical research case studies for practical learning.

  • Regulatory Standards – CDISC, SDTM, and ADaM guidelines.

Eligibility

  • Life sciences graduates (B.Sc., M.Sc., B.Pharm, M.Pharm, BDS, MBBS, etc.)

  • Professionals from clinical research, data management, biostatistics, or pharma sectors.

  • Freshers aiming to enter the SAS programming domain.

Career

  • SAS Programmer

  • Clinical Data Analyst

  • Biostatistician Assistant

  • Statistical Programmer

  • Data Management Specialist in Pharma/Healthcare

Course Duration: 

6 Months Course 

Certification in Business analyst
Diploma SAS in clinical research

The Certification in Business Analyst program is designed to prepare students and professionals for strategic decision-making roles and blends analytical tools, business acumen, and domain knowledge to meet the growing demand for business analysts in healthcare, clinical research, and other industries.

Key Highlights

  • Introduction to Business Analysis – Role, responsibilities, and scope in various industries.

  • Requirement Gathering & Documentation – Elicitation techniques, stakeholder management, and business process modeling.

  • Data Analysis & Visualization – Using Excel, Power BI, Tableau, and SQL for actionable insights.

  • Healthcare & Clinical Research Focus – Understanding business analytics in pharma, CROs, and clinical trial operations.

  • Hands-On Case Studies – Real-time business scenarios for practical learning.

Eligibility

  • Graduates from life sciences, management, IT, and commerce backgrounds.

  • Professionals seeking career transition into business analysis.

  • Freshers aiming to start a career in data-driven decision-making roles.

Career

  • Business Analyst

  • Clinical Business Analyst

  • Data Analyst

  • Process Improvement Specialist

  • Project Coordinator in Pharma/Healthcare

Course Duration: 

3 Months Course 

Advance Diploma in clinical research and clinical time management
Certiication in business analysis

The Advance Diploma in Clinical Research & Clinical Trial Management is a specialized program designed to train graduates and professionals in end-to-end clinical research operations with a strong focus on trial design, execution, monitoring, and regulatory compliance. The course equips students with both theoretical knowledge and hands-on practical skills to excel in the global clinical research industry.

Key Highlights

  • Fundamentals of Clinical Research – Overview of drug development and clinical trial phases.

  • Clinical Trial Management – Planning, budgeting, site selection, and project management.

  • ICH-GCP Guidelines & Regulatory Affairs – Compliance with DCGI, FDA, EMA, and WHO standards.

  • Site Management & Monitoring – Investigator meetings, ethics committee submissions, and monitoring visits.

  • Clinical Data Management – Data collection, validation, and quality assurance.

  • Pharmacovigilance – Drug safety monitoring and adverse event reporting.

  • Practical Exposure – Case studies, mock audits, and interview preparation.

Eligibility

  • Life Sciences, Pharmacy, Medical, Nursing, and Allied Health graduates.

  • Professionals from clinical, pharma, or healthcare sectors seeking career growth.

  • Fresh graduates aiming for a career in clinical trial operations.

Career

  • Clinical Research Coordinator (CRC)

  • Clinical Trial Manager

  • Clinical Research Associate (CRA)

  • Data Management Associate

  • Pharmacovigilance Officer

  • Regulatory Affairs Executive

Course Duration: 

1 Year Course + Internship 

Advance diploma in clinical research & pharmacovigilance
Advance diploma in clinical research & clinical management

The Advance Diploma in Clinical Research & Pharmacovigilance is designed to prepare graduates and professionals for careers in drug development, clinical trials, and drug safety monitoring. This program blends comprehensive theoretical learning with practical, industry-relevant training to meet the growing demand for skilled experts in the global life sciences sector.

Key Highlights

  • Clinical Research Fundamentals – Drug discovery process, trial phases, and study protocols.

  • ICH-GCP Guidelines & Regulatory Affairs – Compliance with DCGI, FDA, EMA, and WHO standards.

  • Pharmacovigilance Principles – Detection, assessment, reporting, and prevention of adverse drug reactions (ADRs).

  • Clinical Trial Management – Planning, site selection, ethics submissions, and monitoring visits.

  • Clinical Data Management – Case report forms (CRFs), database handling, and data validation.

  • Drug Safety Systems – Signal detection, benefit-risk assessment, and post-marketing surveillance.

  • Practical Exposure – Case studies, mock audits, and interview preparation.

Eligibility

  • Graduates in Life Sciences, Pharmacy, Medicine, Nursing, or Allied Health.

  • Professionals in pharma, healthcare, or biotech looking to specialize in drug safety.

  • Fresh graduates aiming for a career in clinical research or pharmacovigilance.

Career

  • Pharmacovigilance Associate / Drug Safety Associate

  • Clinical Research Coordinator (CRC)

  • Clinical Research Associate (CRA)

  • Regulatory Affairs Executive

  • Medical Review Officer

  • Data Management Associate

Course Duration: 

6 Months  Course + Internship 

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