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<p>PG Diploma Advanced Clinical Research & Pharmacovigilance in Bangalore</p>
Bangalore Campus
PG Diploma in Advance Clinical research & PVCDM
Duration - 10 Months
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Scope of The Course
  • Vacancies
    INR 3.5 Lacs to INR 5.5 Lacs PA

    Starting Salary Package

  • INR 3.5 Lacs to 6.0 Lacs
    INR Over USD 261 billion

    Industry Size

  • U$D 16
    25 lac positions globally

    Positions vacant

PG Diploma in Advance Clinical Research & PVCDM

India’s first & largest institute in healthcare management

Real time exposure in hospital facility for hands on practical training in industry partners & hospitals

Additional certifications from CII and ICRI upon completion of training

Industry trainings embedded in course curriculum with practical training at leading hospitals

19000+ alumni network working across the globe

Learn and explore the best of both worlds with India’s top ranked university

Awardee of Presidential Award for contribution in clinical research & healthcare

ICRI has partnered with leading healthcare organizations such as Singhealth

What will you study?


    • Module I – Introduction to Clinical Research
    • Module II – Basic Pharmacology and Pharmacy in Clinical Research
    • Module III – New Drug Development
    • Module IV – Ethical Guidelines in Clinical Research
    • Module V – Ethics in Clinical Research
    • Module VI – Regulations in Clinical Research
    • Module VII – Biostatistics in Clinical Research
    • Module VIII – Specialist Clinical Trials and Clinical Trial Designs
    • Module IX – Clinical Trial Documentation
    • Module X – Quality in Clinical Trials
    • Module XI – Clinical Data Management
    • Module XII – Clinical Trial Management
    • Module XII – Drug Safety and Pharmacovigilance
    • Module XIV – Soft Skills for a Clinical Research Professional


What Will You Become
    • For Doctors: Principal Investigators / Co-investigator / Medical Advisor / Drug Developers / Regulatory Affairs Manager / Clinical Research Physician.
    • For Paramedics, Pharmacists & Life Science Graduates: Medical Writers / Clinical Research Associates / Site coordinators / Clinical Research Manager / Drug Development Associates / Clinical Data Management / Pharmacovigilance Executive / Clinical Trial analyst / Drug Reviewer / Drug Safety Physician & many more
    • For Management Professionals: (with Life Science/Health Science background) Business Development / Clinical Project Management / Clinical Research Management / Regulatory Affairs.
    • Clinical Research Associates: To monitor clinical trials, ensure compliance with the clinical trial protocol, checks clinical sites activities, make on-site visits, CRFs.
    • Clinical Research Investigators: Conduct BA/BE studies, writing / revising SOP, review of protocols, investigators brochures, ICF & CRFs Protocol, CRF & ICF preparations plans and conduct of BA/BEIEC/IRB affairs-GC.
    • Study Coordinators: Provides safety & protection while collecting & managing the study data.
    • Data Manager / Biostatistician: Design, study & predict the seriousness of the disease, seriousness of the disease, evaluate new treatment and effectiveness of medication, participate in research design, data collection, choosing & implementing appropriate methodologies, interpreting the results.
    • Regulatory Affairs Managers: Review & registration of documents, evaluation of technical data, liaison with regulatory authorities.
    • Clinical Trials Auditors: Conduct audits for regulatory function within the trial department to assure compliance with GLP/GCP in accordance with established FDA regulations and company policies & standard operating procedure.
    • Clinical Research Managers: Manage, supervise, train, mentor clinical research staff, approve investigator’s study, budget & contract, review & approve regulatory documents, develop a protocol, approve CRFs, review study data.
    • Business Development Manager: Identify potential clients, establish business relations, responsible for meeting new clients, following up on leads, market research.
    • Drug Safety Associate: Manage & relay drug safety information, maintain current knowledge of global drug safety regulations, summarize clinical safety data, write narratives with medical input, report SADRs to Regulatory Authorities, participate in training on drug safety issues & another task under drug safety.
    • Medical Writer: Documentation, manuscripts, abstracts, external communication tools Clinical Data Manager: Ensures the accuracy & consistency of data prepared for regulatory bodies for reporting purpose.
    • Others: Auditors, Quality Assurance, Patents & IP Related position


    Where will you work:


    • Bioengineering companies- Serum Institute Of India, Panacea Biotech Ltd, GlaxoSmithKline, Bharat Serums
    • CROs - Excel Lifesciences, Clinigene, IQVIA, PARAXEL, Panacea
    • Hospitals – Apollo, Max, Fortis etc
    • Life-Division of IT Companies – Accenture, TCS, Cognizant etc
    • Pharma Company – Cipla, Novartis, Ranbaxy
    • Medical device companies- Abbott Laboratories, Johnson & Johnson, Novartis AG, Siemens Healthineers, General Electric
    • Medical Colleges-  AIMS, BAMC, Maula AZAD, Mahavir Medical College,
    • Cosmetic Companies- Biotique, Lakme, Sugar Cosmetics, Mamaearth
Industry Exposure
  • India’s 1st Institute
  • India’s 1st Institute
  • India’s 1st Institute

    Clinical research Industry: Global & Indian perspective

    • The global clinical trials market size was estimated over 50.0 billion in 2022 and is expected to reach to USD 84.43 Bn by 2030 with a registered CAGR of 5.7% during the forecast period 2022 to 2030.
    • The market was further driven by  COVID-19 pandemic and the importance of making India as a hub for conducting clinical trials. The large number of patients also highlights the growing demand for treatments and immunizations. Currently, 288 medicines and 106 vaccines are in various stages of development, with almost 7.0% of therapeutics in Phase IV, 21.0% in Phase III, and 43.0%, 13.0%, and respectively, Phase II and Phase I.
    • These rules have brought India's regulatory framework on par with U.S. Food and Drug Administration (FDA) norms and now India is among the top choices for global clinical trials. India's clinical trials market is expected to reach $3.15 billion by 2025 with a compounded annual growth rate of 8.7%.
    • A new set of rules in place since 2019 is beginning to make India an attractive destination for big pharma to conduct clinical trials in India.
    • Today, around 50,000 clinical research professionals are required in the clinical research industry.
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