INDIAN COUNCIL OF MEDICAL RESEARCH

Div!!ion of Epidemiology and Communicable Diseases WALK-IN-WRITTEN TESTNNTERVIEW (EMPLOYI\4ENT NOTIFICATION)

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 oi 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 skengths and focus on building and strengthening scientific capabilities and generating a better understanding to aid rn accelerating the development of new diagnostics, new & improved vaccines and lmmunotherapies, drugs for TB.

Following posts are to be filled purely on contractual basis for working under the Flagship programme entitled 'lndia TB Research Consortium' (ITRC) under Division of Epidemiology and Communicable Diseases (ECD), ICIVR Hqrs Office, New Delhi.

lnterested candidates for the various positions mentioned below are invited to appear for the Walk-in-Written TesU lnterview along with 5 copies of their updated Bio dataiCV on 25th May, 2018 reporting, between 09:00 A.M to 10:00 A.M at the following address . Latecomers will not be entertained after

10:30 A.M. under any circumstances.

> Reception hall, lndian Council ol Medical Research,

Ramalingaswami Bhawan,

Ansari Nagar New Delhi-110 029

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1. Post of Consultants (Scientific) Biomedical Research (Quality Assu rance) _-One

s.No.	Details		Req u irements/ln fo rmation
A1.	Name of Posts		Consultant {Screntific) BiomedicalResearch (Quality Assurance
B	No. of Vacancies		One Post
C	EssentralQualiflcation	I	Post Graduate Degree (MD/[,{S/DNB) after IVIBBS with one year of
			demonstrated experience in quality assurance in clinical research from
			reputed lnstitution.
			OR
			Postgraduate diploma after MBBS with 2 years of demonstrated
			experience ln quality assurance in clinical research from reputed
			lnstitution
			OR
			MBBS with four year of clinical experience in Govemment lnstitution of
ttl			which 2 years should be demonskated experience in quality assurance in clinical research from reputed lnstitution.
			OR
			lst class Masters in Medical Pharmacology/N/edical Microbiology with 4
			6 years of demonstrated experience in quality assurance in clinical
lt			research from reputed lnstitution. OR Ph.D in Medical Pharmacology/lVedical l\ilicrobiology with 2 yrs. of
			demonstrated experience in quality assurance in clinical research from
ttt			reputed lnstituton. --.
D	Desirable		)> Experience in preparing Quality Assuance manual for the research
			Prog ramme/project(s).
			> Evaluating quality events, incidents, queries and complaints and
			handling compliance issues. ) Experience in managing and maintarning databases for quality
			systems.) Able to prepare SOPs for trial conduct. )> Thorough knowledge of GCP, ICH guidelines and regulatory
			requirements for clinical trial conduct.
E F	Nature of Duties e		Limited as on date. u p to 70 years) Ensure that all processes contributing to the performance of a
			clinical kial are conducted propedy.! Troubleshoot clinical trials and activities.
			> Prepare and assist in preparing annual reports and quality kending
			reports.
			> Report the status of the quality levels of the staff, systems and
			production activities.
I			> Preside over improvement programmes.) Keep upto date with all quality and compliance issues.
			> The job may require frequent travel to sites for quality assurance
			check and !ality tlqnagq!!9Il!
	Consolidated		lvlaximum Rs.70,0001 per month depending upon experience and
	Emoluments		knowledge.
			_
H	Tenure		Two Years
	Syllabus for Written		Degree level related to project work, if written Test conducted
	Examination

J Place of Work lC[/R Hqrs.

)

2. Post of Consultant (Clinical Coordinator) : 0ne

S.NO A1		Details Name of Posts	I ilqcirements/lnformation . Consultant (Clinical Coordinator)
B		No. of Vacancies	One Post
C		Essential Qualification	Post graduate Degree (MD/MS/DNB) after lr/BBS with 1 year
			experience in clinical trials/ studies from reputed lnstitution.
			OR
			Post graduate Diploma in lVledical subject after MBBS wilh 2 year
			experience in clinical trialsistudies from reputed lnstitution.
			OR
			MBBS with 4 year experience in clinical trials/studies from reputed
			lnstitution.
			OR
			lst class lVasters in Medical Pharmacology/Medical Microbiology with
			4-6 years of demonstrated experience in clinical trials/studies lrom
			reputed Institutions.
			OR
			Ph.D in Medical Pharmacology/Medical Microbiology with 2 yrs. of
			demonstrated experience in clinical trials/studies from reputed
			lnstitutions.
D		Desirable Experience	r Prepare the manual for the Project activities and the annual
			reports on progress.
			> Able to prepare SOPs for trial conduct.
			r Thorough knowledge of GCP, ICH guidelines and regulatory
			requirements for clinical kial conduct.
			> Experience in co-ordinating project activities with sites i Good communrcation skills
E		e	Limited as on date. u pto 70
F		Nature of Duties	Coordination of project mp men onata tesS
	I		. Communication to lnternational and National agencies.
			. Preparation of programme manual/flnancial documents, Data
			Programme progress Report, Report writing.
			. Drafting letters for sending to various organizations,/Organizing
			meetings of various Expert Groups/anangements for the
			meetings/preparing reports
			. Any other work that may be assigned from time to time by the
			concerned ICIVR officials.
			. The;ob may require travel to the kial sites for co-ordination, data
			management and attend i outstation meetin S
		Consolidated	l\ilaximum Rs.70,0001 per month depending upon experience and
		Emoluments	knowledge.
H		Ten u re	Two Years
I		Syllabus for Written	Degree level related to project work, if written Test conducted
		Examination
J		Place of Work	CIVR Hqr!.

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3. Post of Consultants (Scientific) Pre-clinical Research-one

S.NO.		Details
1	A	Name of Posts
	B	No. of Vacancies
	C	Essential Qualiflcation

I

I

D Desirable

Ee F Nature of Duties

Requirements/lnformation Consultant (Scientific) Pre-Clinical 0perations

One Post Post Graduate Degree ([/D/MSiDNB) after IV1BBS with one year of demonstrated experience in pre-clinical studies from a reputed lnstitute/Pharma industry/Biotech industry.

OR Postgraduate diploma after IVlBBS with 2 years demonstrated experience in pre-clinical studies (in vitro assays, regulatory toxicology studies/ animal toxicology/animal pharmacology study) from a reputed lnstitute/ Pharma industry/Biotech industry.

OR MBBS with four year demonstrated experience in pre-clinical studies (in vitro assays, regulatory toxicology studies/ animal toxicology/animal pharmacology study) from a reputed lnstitute/ Pharma industry/Biotech industry.

OR

1st Class M.sc. in Medical lVicrobiology/ lVedical

Pharmacology/lmmunology/ from a recognized University with 4-6 years of demonstrated experience in pre-cllnical studies (in vitro assays, regulatory toxicology studiesi animal toxicology/animal pharmacology study) from Reputed Institute/ Pharma industry/Biotech

industry. OR

1.t Class lvl. Pharm (Pharmaceutical sciences/toxicological sciences) with 4-6 years of demonskated experience in pre-clinical studies (in vitro assays, regulatory toxicology studies/ animal toxicology/animal pharmacology study) from a reputed Institute/ Pharma industry/Biotech

lindustry.

OR Ph.D in lvedical Pharmacologyi Medical lVicrobiology with 2 yrs. of demonstrated experience in quality assurance in pre-clinical studies (in vitro assays, regulatory toxicology studies/ animal toxicology/animal pharmacology study) from a reputed lnstitute/ Pharma industry/Biotech

lqqlustry . PhD in Medical pharmacology/medical microbiology/immunology from a recognized University . Strong knowledge of clinical research process and medical terminology. . Understanding of GCP/lCH guidelines. . Knowledge of regulatory requirements and guidelines goveming clinical research. . Ability to work successfully within a crossfunctional team _' Good Scientiflc writing/Communication skills Knowledge of computer applications or business intelligencetools/data

MlqSernglrt ^{/ qata synthesis _Limited as on date: up to 70 years}

.To manage all clinical aspects of study including assessing operational feasibility and recommending study execution plan; deve loping and _llqnaS!!S comprehensive stu timelines and

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metrics.
.Prepare the pre-clinical study protocols related to various new
candidates for pre-clinical studies along with the budget.
.ldentify sites and prepare documents for site feasibility for
undertaking the pre-clinical studies. .Review and prepare progress report of the various
ongoing/completed studies.
.To participate in Selection and managemenUOversight of external
I				vendors and develops vendor specilications; review vendor reports,
				budgets and metrics
I				.To provide study specific training and leadership to Clinical Research
				Staff, including CRO, CRAs, Sites and other contract personnel
				.To plan, Execute and Lead study specilic meetings
				.To participate in Site monitoring visits and oversee clinical monitoring
I				activities ensuring compliance with Good Clinical Practices
				.To prepare and/or review study related Standard Operating
				procedures and Documents
				. To develop and manage study budget and maintain it within
				financial goals
il			Consolidated Emoluments	o The job may require travel to the trial sites for assessmenU mq!!oil0lqv!c! q! q!q!qi!s qqt9!4r9[a99!D gs l\,4aximum Rs.70,000/-per month depending upon experience and !roqgqsq
	H		Tenure Syllabus for Written	ITwo Years Degree level related to project work, if written Test conducted
			Examination
	J		Place of Work	lCl\.4R Hqrs

SELECTION PROCEDURE: lnterview will be conducted to the eligible candidates. However, if more number of candidates are found eligibie for the post advertised, Written TesU Skill Test may also be conducted on the same day before final round of lnterview. The candidates should bring 5 copies of biodata along with all original certiflcates of educational qualifications (from SSC onwards), experience, Aadhaar Card, Community Certificates along with one set of photocopres of the same duly attested (can be self attested) along with a passport size photograph for attending the Wriften Test/ lnteruiew. No Tfu DA will be paid for attending the Written TesU Interview. The recruited project staff is eligible for leave as per rules and will have to give an undertaking before joining.

GENERAL CONDITIONS: The mnditions of employment will be the same as that of the prolect staff on contract basis. The candidates have no right to claim for any regular employment at this lnstitute. The appointing authority has the right to accepU relect any application without assigning any reason(s) and no correspondence in this matter will be entertained. Age, Qualification, experience etc., will be reckoned as on the date of walk-in-written tesV lnterview.

Note: No electronic device including Calculator and l\,4obile phones are allowed in the examination Hall

For any query, Please contact at 01 1-26589169

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Admrnistra For Director General

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	Start Date	End Date
Interviews		25-May-2018

• Organization : Indian Council Of Medical Research
• Organization City, State : , delhi
• Organization Website : http://icmr.gov.in