"Master Clinical Research with India's Leading CRO Experts"

Learn from professionals who conduct real clinical trials.

Get  certified.

"Master Clinical Research with India's Leading CRO Experts"

Learn from professionals who conduct real clinical trials.

Get  certified.

15+
Yrs Industry Experince

Launch your career in the fastest-growing healthcare sector services
Powered by OSSINC — 15+ Years of Excellence in Clinical Research Operations
Trained by Active CRO Professionals
Industry-Level Certification
Placement Guidance Support

ABOUT THE  INSTITUTE

"Why Learn Clinical Research from OSSINC Institute of Clinical Research?"

We don't just teach clinical trials we conduct them

OSSINC Institute of Clinical Research is backed by On Site Services Incorporation (OSSINC), a leading Contract Research Organization (CRO) and Site Management Organization (SMO) with over 15 years of hands-on experience in managing clinical trials across India.

Our courses are designed and delivered by professionals who are actively involved in:

  • Clinical Research Operations for global pharma sponsors
  • Site Management across multiple therapeutic areas
  • Regulatory Affairs and medical writing
  • Pharmacovigilance and data management

OUR COURSES CHOOSE YOUR PATH

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 recognized certificate that boosts your CV and prepares you for entry-level opportunities in the clinical research industry.

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.

WHAT OUR STUDENTS SAY
Testimonials

Vivek Kumar

(Senior CRC)

“Training at OSSINC gave me a clear understanding of clinical research fundamentals. The mentors explained concepts in a simple and practical way. This guidance helped me grow into my current role as a Senior CRC.”

Rishabh Bajpayee

(Senior CRA)

“The OSSINC program is practical and industry-focused. The skills I learned here are exactly what I use in my job today. It played an important role in preparing me for the CRA position.”

Anklesh Pathak

(QA Head)

“OSSINC focuses on real learning, not just course completion. The training strengthened my understanding of regulatory and quality processes. A reliable place for serious learners.”

Shreya Mishra

(Senior CRC)

“I started as a beginner, and OSSINC helped me build confidence step by step. The mentors are supportive and the training is well-structured. Today I handle my role as a Senior CRC with confidence.”

Aman Dwivedi

(Site Manager)

“OSSINC provided me with practical insight into site management and clinical research operations. The learning approach is simple, clear, and easy to follow. A valuable experience.”

Kunal Kishore

(Senior CRA)

“OSSINC gave me the right direction in clinical research. The curriculum is updated, and continuous guidance made a real difference in my career journey.”

Join OSSINC and start your journey in Clinical Research from foundation to professional expertise.

Frequently Asked Questions? (FAQs)

Got Questions? We've Got Answers

Anyone with a background in Life Sciences, Pharmacy, Nursing, Medicine, or Allied Health. No prior clinical research experience required for Course 1.

Course 1: Self-paced online learning with e-books and MCQ assessments.

Course 2: Instructor-guided with live guest lectures, case studies, and MCQ assignments.

We provide comprehensive placement guidance and support including resume building, interview prep, and job application assistance.

No! Course 2 is a complete, standalone program that covers all foundational topics from Course 1 in detail, plus advanced content.

Choose Course 1 if you want a quick, budget-friendly introduction

Choose Course 2 if you want comprehensive, job-ready training (recommended for serious career seekers)

After payment, you'll receive login credentials via email. Access your course dashboard to start learning immediately.

Please refer to our [Terms & Conditions] for detailed refund and cancellation policies.

Download our [Franchise Brochure] or [Schedule a Call] with our business development team to learn more.

Our courses are technically supported by Bio Medical Research Foundation (BMRF). For any technical issues, contact us at contact@ossinc.org.

Contact & Support
"We're Here to Help — Get in Touch!"


  • Email Us:

    General Inquiries

    contact@ossinc.org

    Course Enrollment

    institute@ossinc.org

    Call/WhatsApp

    +91-7521001901


  • Visit Us:

    OSSINC

    Institute of Clinical Research


      Plot No 104, Hardoi Road, Lucknow - 226003, Uttar Pradesh, India

    Office Hours

    Monday - Saturday: 10:00 AM - 6:00 PM
    Sunday: Closed


  • Quick Support

    Chat with Us on WhatsApp

    7521001902


      Get instant answers to your queries!

    Connect with OSSINC Institute:

    Learn More About.

    Visit www.ossincinstitute.com

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description
OSS001
Foundations
1 Month Self-Paced

Certificate in Clinical Research Foundations.

file_download SYLLABUS
workspace_premium
OSS002
Advanced
3 Months Instructor-Led

Advanced Clinical Research Practices Program.

file_download SYLLABUS