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Dr. Ashok Rattan, Chief Executive, Fortis Clinical Research Ltd & Adviser, Religare SRL Diagnostics,  Fortis / Escorts Hospitals, Delhi & NCR Careers in Clinical Research
Dr. Ashok Rattan MBBS, MD, MAMS ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],MBBS MD MAMS
Pick a job you like,  and you will never have to work in your life Either be so talented that you get what you want, Or  Accept what you get and  act as though you always  Wanted what you have been given
New Drug Discovery and Development (Timelines) DISCOVERY/SCREENING SYNTHESIS AND PURIFICATION ANIMAL TESTING PHASE II PHASE I SHORT-TERM PHASE III LONG-TERM PHASE IV ADVERSE REACTION SURVEILLANCE PRODUCT  DEFECT REPORTING PRE-CLINICAL RESEARCH CLINICAL  STUDIES NDA  REVIEW POST-MARKETING 24 + 18 months. AVG:  5 YEARS AVG:  12 MOS. IND NDA APPROVAL
TARGET  IDENTIFICATION  & VALIDATION R&D Technology HIT IDENTIFICATION  LEAD SEARCH  & OPTIMIZATION CANDIDATE  SELECTION  GLP PHASE PHASE I-II PHASE II - III EXPLORATORY RESEARCH DRUG DISCOVERY DRUG PROFILING PRE- DEVELOPMENT DEVELOPMENT GENOMICS PROTEOMICS PHARMACOGENETICS BIOINFORMATICS HTS ASSAY DEVELOPMENT SUBSTANCE LIBRARY MOLECULAR MODELING COMBINATORIAL CHEMISTRY IN VITRO &  ANIMAL PHARMACOLOGY TOXICOLOGY NEW FORMULATION PILOT PLANT PHARMACOGENETICS DATA MINING DATA BASE
5000 compounds  evaluated Phase-I 20-100 healthy volunteers 0 2 4 6 8 10 12 16 14 Years Phase-II 100-500 patient volunteers Phase-III 1000-5000 patient volunteers Review and approval by Food & Drug Administration 1 Compound approved 5 INDs Discovery and preclinical testing Source: Tufts Centre For Study Of Drug Development in C&EN, June  2000 Bringing a new drug to the market can take 15 years
Cost of bringing a new drug to the market is 800M to 1B US$
Understand Disease & Identify unmet needs Select Mechanism/ Target Design NCEs & Screens Virtual  Screening Synthesize  NCEs Convert Lead-to-IND Candidate New Drug Discovery Road Map Preclinical work-up IND directed  regulatory studies Convert Hit-to-Lead Screen/ Identify Hit
IND Approval Investigator’s brochure Protocol Approval for Phase 1 Select research site
Activities ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Clinical Trials Win Win Relationship CRO/ SMO/ ARO Fee for service,  expand research capacity,  work satisfaction Sponsors  Regulatory approval, Publication, Enhanced healthcare,  Sales & Profits Patients Improved care, decreased expenses,  new therapies Investigator Fee for service,  Expand Research capacity,  Academic interest / publication
 
Career opportunities in  Clinical Research
Why Join Clinical Research ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Advantage India Language Patient pool Cost Speed English speaking staff Large pool of treatment naiive patients 30 – 50% of USA or EU cost Fast recruitment Regulatory International Quality  Parallel Studies Schedule Y 2005 Quality
Success Speed   Cost   Quality
People involved in clinical trial in USA Sponsor staff CRO staff Investigators Other site staff 78,000 44,000 50,000 35,000
Supply  &  Demand  Manpower  2010 Sponsor staff CRO staff Investigators Other site staff 1,000 6,000 2,000 4,000 200 1,000 300 400
Career Pathways ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Where ? ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Roadmap to success
Roadmap 1 For medical graduates ,[object Object],[object Object],[object Object],Medical Adviser, Regulatory Affairs Manager, Medical Monitor, Medical Writer In 5 to 15 years to be: ,[object Object],[object Object]
Roadmap 2 for Pharma / graduates ,[object Object],[object Object],In 5 to 15 years expect to become: Clinical Team leader, Project Manager,  Manager (Clinical Operations),  Manager (QA), Clinical Study manager,  Regulatory manager In 2 to 5 years you may become ,[object Object]
Roadmap 3 ,[object Object],[object Object],[object Object],In 2 to 5 years expect to become ,[object Object],In 5 to 15 years you will be ,[object Object]
Roadmap 4 ,[object Object],[object Object],[object Object],In 2 to 5 years time, expect to become Manager BD, Manager (Clinical Trial supplies),  Manager (Accounts), Manager (HR),  Manager (Training) Head (HR), Head (BD), CFO, Head (Training & QA ) In 5 to 15 years time, you could be
[object Object],[object Object],[object Object],[object Object],[object Object]
Always remember we can not spell success without “U”
Education Change of behavior Cognition Psychomotor   Affective Act of knowing   Skills   Attitude, Motivation Knowledge is power  Skills come from drill “I can” is more important than IQ DOMAINS
[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
“ It is not the strongest of species that survive,  nor the most intelligent,  but the ones most responsive to changes” Charles Darwin (1809-1882) Life's battles don't always go To the stronger or faster man,  But sooner or later the man who wins  Is the one who thinks he can.   Attributed to Author Napoleon Hill circa 1973

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Careers In Clinical Research 2009

  • 1. Dr. Ashok Rattan, Chief Executive, Fortis Clinical Research Ltd & Adviser, Religare SRL Diagnostics, Fortis / Escorts Hospitals, Delhi & NCR Careers in Clinical Research
  • 2.
  • 3. Pick a job you like, and you will never have to work in your life Either be so talented that you get what you want, Or Accept what you get and act as though you always Wanted what you have been given
  • 4. New Drug Discovery and Development (Timelines) DISCOVERY/SCREENING SYNTHESIS AND PURIFICATION ANIMAL TESTING PHASE II PHASE I SHORT-TERM PHASE III LONG-TERM PHASE IV ADVERSE REACTION SURVEILLANCE PRODUCT DEFECT REPORTING PRE-CLINICAL RESEARCH CLINICAL STUDIES NDA REVIEW POST-MARKETING 24 + 18 months. AVG: 5 YEARS AVG: 12 MOS. IND NDA APPROVAL
  • 5. TARGET IDENTIFICATION & VALIDATION R&D Technology HIT IDENTIFICATION LEAD SEARCH & OPTIMIZATION CANDIDATE SELECTION GLP PHASE PHASE I-II PHASE II - III EXPLORATORY RESEARCH DRUG DISCOVERY DRUG PROFILING PRE- DEVELOPMENT DEVELOPMENT GENOMICS PROTEOMICS PHARMACOGENETICS BIOINFORMATICS HTS ASSAY DEVELOPMENT SUBSTANCE LIBRARY MOLECULAR MODELING COMBINATORIAL CHEMISTRY IN VITRO & ANIMAL PHARMACOLOGY TOXICOLOGY NEW FORMULATION PILOT PLANT PHARMACOGENETICS DATA MINING DATA BASE
  • 6. 5000 compounds evaluated Phase-I 20-100 healthy volunteers 0 2 4 6 8 10 12 16 14 Years Phase-II 100-500 patient volunteers Phase-III 1000-5000 patient volunteers Review and approval by Food & Drug Administration 1 Compound approved 5 INDs Discovery and preclinical testing Source: Tufts Centre For Study Of Drug Development in C&EN, June 2000 Bringing a new drug to the market can take 15 years
  • 7. Cost of bringing a new drug to the market is 800M to 1B US$
  • 8. Understand Disease & Identify unmet needs Select Mechanism/ Target Design NCEs & Screens Virtual Screening Synthesize NCEs Convert Lead-to-IND Candidate New Drug Discovery Road Map Preclinical work-up IND directed regulatory studies Convert Hit-to-Lead Screen/ Identify Hit
  • 9. IND Approval Investigator’s brochure Protocol Approval for Phase 1 Select research site
  • 10.
  • 11. Clinical Trials Win Win Relationship CRO/ SMO/ ARO Fee for service, expand research capacity, work satisfaction Sponsors Regulatory approval, Publication, Enhanced healthcare, Sales & Profits Patients Improved care, decreased expenses, new therapies Investigator Fee for service, Expand Research capacity, Academic interest / publication
  • 12.  
  • 13. Career opportunities in Clinical Research
  • 14.
  • 15. Advantage India Language Patient pool Cost Speed English speaking staff Large pool of treatment naiive patients 30 – 50% of USA or EU cost Fast recruitment Regulatory International Quality Parallel Studies Schedule Y 2005 Quality
  • 16. Success Speed Cost Quality
  • 17. People involved in clinical trial in USA Sponsor staff CRO staff Investigators Other site staff 78,000 44,000 50,000 35,000
  • 18. Supply & Demand Manpower 2010 Sponsor staff CRO staff Investigators Other site staff 1,000 6,000 2,000 4,000 200 1,000 300 400
  • 19.
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  • 26.
  • 27. Always remember we can not spell success without “U”
  • 28. Education Change of behavior Cognition Psychomotor Affective Act of knowing Skills Attitude, Motivation Knowledge is power Skills come from drill “I can” is more important than IQ DOMAINS
  • 29.
  • 30. “ It is not the strongest of species that survive, nor the most intelligent, but the ones most responsive to changes” Charles Darwin (1809-1882) Life's battles don't always go To the stronger or faster man, But sooner or later the man who wins Is the one who thinks he can. Attributed to Author Napoleon Hill circa 1973