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Build Your Career in Clinical Research

Explore globally relevant online certification courses designed by industry professionals.
Clinical Research is among the fastest-growing fields in healthcare — connecting science, innovation, and patient safety.
Our programs help students and professionals learn, apply, and grow through structured
content, interactive modules, and expert guidance.

Certificate in Clinical Research Foundations

CODE: OSS001

Level: Beginner | Duration: 1 Month | Mode: Self-Paced Online

Learn the Basics at Your Own Pace — Perfect for Beginners

Kick-start your journey in clinical research with this flexible 4-week program. Designed for beginners, it introduces how clinical trials are designed, approved, and managed — covering core areas like GCP, ethics, safety, and regulatory documentation. Each module includes self-tests to help you master concepts before moving forward.

Topic Covered

    • Introduction to Clinical Research with History
    • Drug Development Process & Its Phases
    • Basics of ICH-GCP
    • Ethics Committees
    • Role & Responsibilities of Investigator
    • Roles & Responsibilities of Sponsor /CRO
    • Medical Writing
    • Terminologies & Glossary

    • Study Design (RCT, Blinded, Placebo)
    • Study Startup
    • Protocol & Case Report Forms (CRF and eCRF)
    • Informed Consent Process
    • Essential Documents (TMF & eTMF)
    • Laboratory Management
    • Vendor Management
    • Monitoring of Clinical Trials
    • Audit & Inspections
    • Test 2 → Unlock next module

    • Pharmacovigilance Basics (SAE, ADR & AE Reporting)
    • SAE reporting & Compensation
    • 21 CFR Part 11
    • CRF Design
    • Clinical Data Management (EDC, Queries, Validation)
    • Introduction to Biostatistics in Research
    • Unblinding of Drugs
    • Test 3 → Unlock next module

    • Overview of Regulatory Authorities (FDA, EMA, CDSCO)
    • ICMR Guidelines
    • NDCTR 2019 (India Focus)
    • CDSCO & Application process
    • Final Assessment: MCQ + Case Study

    Certificate of Completion

Who Can Enroll

Ideal for students and beginners from science and healthcare backgrounds, including:

  • B.Sc / M.Sc in Life Sciences, Biology, Microbiology, Biotechnology
  • B.Pharm / M.Pharm / Pharm.D
  • BPT / MPT (Physiotherapy)
  • BDS / MDS, MBBS, BHMS, BAMS, Nursing graduates
  • Medical laboratory technologists & allied health professionals
  • Anyone from a science background exploring Research Careers

Outcome

Gain a strong conceptual base, practical understanding, and a industry accepted certificate that boosts your CV and prepares you for entry-level opportunities in the clinical research industry.

Sign up to explore the Course in detail.
Expert-Led
Powered by Online Lectures by Industry Experts. Additional Knowledge Bank & Presentation for in Depth Understanding

Certificate in Advanced Clinical Research Practices

CODE: OSS002

Level: Advanced | Duration: 3 Months | Mode: Instructor-Led Online

Master the Real-World Applications of Clinical Research

This comprehensive 12-week program offers advanced, hands-on learning for those who want to work professionally in clinical research. Through expert-led live sessions, case studies, and assignments, you’ll understand how global trials are designed, monitored, and reported in compliance with international regulations.

Topic Covered

    • Introduction to Clinical Research with History
    • Drug Development Process & Its Phases
    • Basics of ICH-GCP
    • Ethics Committees & Required SOP
    • Role & Responsibilities of Investigator
    • Roles & Responsibilities of Sponsor / CRO
    • Medical Writing, Terminologies & Glossary
    • Developing Research Sites
    • Online Lecture 01

    • Study Design (RCT, Blinded, Placebo)
    • Study Startup & Protocol Development
    • Case Report Forms (CRF and eCRF)
    • Informed Consent Process
    • Essential Documents (TMF & eTMF)
    • Laboratory & Vendor Management
    • Monitoring of Clinical Trials
    • Audit & Inspections
    • Online Lecture 02

    • Pharmacovigilance Basics (SAE, ADR & AE Reporting)
    • SAE Reporting & Compensation
    • 21 CFR Part 11 Compliance
    • Clinical Data Management (EDC, Queries, Validation)
    • Statistical Software Overview: SAS, SPSS, R
    • Global Case Safety Report (ICSR) Workflow
    • Introduction to Biostatistics in Research
    • Unblinding of Drugs
    • Online Lecture 01

    • Overview of Regulatory Authorities (FDA, EMA, CDSCO)
    • ICMR Guidelines & NDCTR 2019 (India Focus)
    • CDSCO & SUGAM Portal (Online Application Process)
    • Online Lecture 01

    • Essential Communication Skills
    • Final Assessment: MCQ & Case Study
    • Course Revision Lecture 01
    • Certificate of Completion

Who Can Enroll

Ideal for graduates and professionals seeking in-depth, career-oriented training:

  • B.Sc / M.Sc (Life Sciences, Microbiology, Biotechnology, Biochemistry, Chemistry)
  • B.Pharm / M.Pharm / Pharm.D
  • MBBS / BDS / BAMS / BHMS / Nursing / Allied Health graduates
  • Professionals from CROs, hospitals, pharma, or regulatory backgrounds
  • Candidates who have completed Course 1 (optional but not required)
  • Anyone aiming for roles like CRA, CRC, PV Officer, Data Manager, QA

Outcome

Develop advanced practical skills, global regulatory awareness, and interview-ready confidence to succeed in the clinical research, pharmacovigilance, or data management sectors.

Sign up to explore the Course in detail.