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STARTING SALARY PACKAGE

INR 3.5 Lacs to INR 5.5 Lacs PA

INDUSTRY SIZE

INR Over USD 261 billion

POSITION VACANT

25 lac position globally

ICRI Campus

ICRI Campus


Course Description

01.

ICRI’s MSc Clinical Research program is an award-winning program and is India’s first &to date the most sought-after program within the science fraternity.

02.

M.Sc. Clinical Research consists of various human experiments and studies.
It is a broad concept with various components, such as clinical research activities, drug management research, drug manufacturing, determining the right dosages of medications for human consumption, and the effects of medications on the human body, among others.

03.

The master's degree in clinical research offers an advanced study of the sub-disciplines of epidemiology, data management, and biostatistics.
Along with the curriculum's theoretical components, this program also focuses on teaching students how to use their knowledge and skills in the real world.

04.

The comprehensive curriculum enhances the avenues available to students when they step into the industry for faster career scope in Clinical Research.

05.

The mix of Clinical Research, Clinical Data Management, Medical Writing, and Pharmacovigilance curriculum along with the Management Module and Soft Skills in the course ensures a head start to move up the corporate ladder faster.

Industry

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.

Curriculam

SEMESTER I

  • Emerging trend of Management
  • Clinical Research Overview
  • Regulation & Ethics in Clinical Research
  • Site Management organization
    (SMO)*
  • Perspectives in Clinical evaluation
  • Statistics for Management

SEMESTER II

  • Molecular mechanism of drug action
  • Preclinical Evaluation of Drugs
  • GMP and GLP *
  • Pharma Regulatory Affairs
  • Global Regulations
  • Pharmacovigilance 1
  • Statistical Analytical System

SEMESTER III

  • Central Lab & Medical Therapeutic Area
  • Pharmacology-I
  • Pharmacovigilance-II
  • Clinical Trial Management
  • Designing Clinical Trials
  • Argus training
  • Minor Project

SEMESTER IV

  • Advanced Clinical Data Management
  • Advanced Medical Writing
  • Pharmacology-II
  • Research Methodology
  • Clinical Oracle
  • Soft skill Training and Personality Development
  • Internship
  • Project Work/Dissertation

What You Will 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, Mama earth

Why ICRI Why ICRI?
  • ICRI has been India’s first & most awarded institution in Clinical Research & Healthcare since 2004.

  • ICRI has 19000+ Alumni network working across the globe

  • Awardee of Presidential Award for contribution in Clinical Research & Healthcare sector along with 21 more industry specific awards such as India Today Awards, Star TV Awards, ET Now, Higher Education Excellence Awards, Saksham Education Award etc for contribution in Aviation, Healthcare & logistics Management

  • India’s first book on clinical research and pharmacovigilance was launched by ICRI.

  • It is the first institute to launch a PhD in Clinical Research and the first international and national conference in clinical research.

  • ICRI has 2500+ industry partners for internship programs and final placements.

  • ICRI is generating 100% placements every year with an average salary package of INR 4.5 Lac PA to INR 7.0 Lac PA
Placements PLACEMENTS ARE PROVIDED WITH

Did You Know

Clinical Research Industry

Key factors

MSc in Clinical Research-2 Years (UGC Recognized)

Duration

Eligibility

Admission Procedure

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