The lndian Council of Medical Research (ICMR), New Delhi, the apex body in lndia for the formulation, coordination and promotion of biomedical research, is one of the oldest medical research bodies in the world. The Govt. of India through lndian Council of Medical Research (ICMR) has initiated its flagship program by establishing an "lndian TB Research Consortium" to advance technology and product development by harnessing interdisciplinary expertise and regional complementary strengths and focus on building and strengthening scientific capabilities and generating a better understanding to aid accelerating the development of new diagnostics, new & improved vaccines and immunotherapies, drugs for TB.
Post : Consultant (Clinical Coordinator)
The Govt. of India through lndian Council of Medical Research (ICMR) has initiated its flagship program by establishing an "lndian TB Research Consortium" to advance technology and product development by harnessing interdisciplinary expertise and regional complementary strengths and focus on building and strengthening scientific capabilities and generating a better understanding to aid accelerating the development of new diagnostics, new & improved vaccines and immunotherapies, drugs for TB.
Following post is to be filled purely on contractual basis for working under the programme entitled 'lndia TB Research Consortium' (ITRC) under Division of Epidemiology and Communicable Diseases (ECD), ICMR Hqrs Office, New Delhi.
Essential Qualification
Post Graduate Degree (MD/MS/DNB) with one year of demonstrated experience of clinical research
OR
Post Graduate Diploma in clinical research after MBBS /BAMS with 2years of demonstrated experience in clinical research
OR
Ist class Masters (MSc/ M.Pharma) in medical Pharmocology/Biotechnology/Clinical Research/Microbiology/Biochemistry with 4-6 years demonstrated experience in clinical research
Desirable Experience
• Able to prepare SOPs and related documents for clinical trial conduct
• Thorough knowledge and understanding of ICH GCP guidelines and relevant regulatory requirements for clinical trial conduct.
• Experience in co-ordinating project activities
• Good communication skills
Age : Limited as on date: up to 70 years
Nature of Duties
• Coordination of all trial related activities and implementation at the sites.
• Communication to International and National agencies.
• Medical Writing
• Preparation of essential documents including study protocol, CRFs, ICDs, etc.
• Plan, coordinate and conduct site activities including site selection /assessment, prepare monitoring plans, conduct monitoring checks and site visits/report as required.
• Trial Data review and checks for accuracy and adequacy
• Any other work that may be assigned from time to time by the concerned ICMR officials.
• The job may require travel to the trial sites and attending outstation meetings.
• Preparation of financial documents, Data Programme Report, Report writing
• Drafting letters for sending to various organizations.
Consolidated Emoluments : Rs.70,000/- per month consolidated
Tenure : Two Years
Syllabus for Written Examination : Degree level related to project work, if written Test conducted
Place of Work : ICMR Hqrs.
Interested candidates for the various positions mentioned below are invited to appear for the Walkin- Written Test interview along with 5 copies of their updated Bio data CV with one photograph on 8th January 2019 between 09:00 A.M to 10:00 A.M at Indian Council ofMedical Research, Ansari Nagar, New Delhi-110 029.
The candidates may submit their CV at teamtbconsortium@gmail.com ; vadehra.icmr@gmail.com before or on 7th January till 5:00 pm. Latecomers will not be entertained after 10:30 A.M. under any circumstances.
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