S.NO.

Details

Requirements/Information

1.

A

Name of Posts

Consultant (Finance)

B

No. of Vacancies

One Post

C

Essential Qualification

Retired Government employee with Bachelors Degree

drawing pay in the Pay Band Rs.9300-3480 +GP of

Rs.5400 (Pre-revised) and above at the time of

retirement with at least 10 years experience in finance

and accounts matter.

D

Desirable

Proficiency in the latest Accounting packages and

Knowledge of MS Office (Word, Power Point, Excel)

along with latest version of Tally.

E

Age

Upto 70 years

F

Nature of Duties

Responsible for all financial work of ITRC

Maintaining accurate records of expenditure

incurred in the project; timely preparation of

UC&SE

Systematic Accounting of Funds received for

the project

Ensure timeliness in completing the tasks

assigned

Preparing budget estimates for the research

programmes

Preparation of Annual Reports of Income &

Expenditure

Any other work that may be assigned from

time to time by the Management

G

Consolidated

Max. Rs.60,000/- depending upon experience and

Emoluments

knowledge

H

Tenure

Two Years

I

Syllabus for Written

Degree level related to project work, if written Test

Examination

conducted

J

Place of Work

ICMR Hqrs.

K

Date & Time of

23th February, 2018 strictly between 09:00 A.M to 10:00

Written Test/

A.M

Interview

S.NO.

Details

Requirements/Information

1.

A

Name of Posts

Consultant (Administration)

B

No. of Vacancies

One Post

C

Essential Qualification

Retired Government employee with Bachelors Degree

drawing pay in the Pay Band Rs.9300-3480 +GP of

Rs.5400(Pre-revised) and above at the time of

retirement with at least 10 years experience in

administration

D

Desirable

Proficiency and Knowledge of MS Office (Word,

Power Point, Excel) along with latest version of Tally.

E

Age

Upto 70 years

F

Nature of Duties

Responsible for all administrative work

Maintaining log files

Processing matters for sanction of the projects as

recommended by expert groups of ITRC.

Responsible for all the logistic support in

convening meeting of experts; Interaction with

experts etc

Systematic Accounting of Funds for research

projects

Ensure timeliness in completing the tasks assigned

Preparing budget estimates

Preparation of Annual Reports

Any other work that may be assigned from time to

time by the Management

G

Consolidated

Max. Rs.60,000/- depending upon experience and

Emoluments

knowledge

H

Tenure

Two Years

I

Syllabus for Written

Degree level related to project work, if written Test

Examination

conducted

J

Place of Work

ICMR Hqrs.

K

Date & Time of

23th February, 2018 strictly between 09:00 A.M to 10:00

Written Test/

A.M

Interview

S.NO.

Details

Requirements/Information

1.

A

Name of Posts

Consultant ((Legal and Compliance)

B

No. of Vacancies

One Post

C

Essential Qualification

LLB from recognized and reputed institute with at least 8

years of experience or LLM from recognized and reputed

institute with at least 6 years of experience in contracts,

projects/Programme

management,

funding/research

organizations.

OR

Retired Government employee with LLB from recognized

and reputed institute drawing pay in the Pay Band Rs.9300-

3480 +GP of Rs.5400(Pre-revised) and above at the time of

retirement with at least 10 years experience in legal matter.

D

Desirable

Work experience preferably in government institutions.

E

Age

Upto 70 years

F

Nature of Duties

A. Legal risk

1.Provide necessary legal support for any contractual

arrangements to be put in place at ITRC

3.Provide legal guidance for program components

4.Drafts, reviews and provide legal advice on tender

documents

5.To manage the legal due diligence process and

reviews the diligence reports

B. Process development

6.

To reviews, drafts and opines on contracts/

agreements/ MOUs and internal SOPs and ensure that

they are in compliance with all statutory or legal

requirements

C. Documentation and compliance

7.

To monitor compliance with statutory and

organisational obligations and advises accordingly

G

Consolidated

Max. Rs.60,000/- depending upon experience and

Emoluments

knowledge.

H

Tenure

Two Years

I

Syllabus for Written

Degree level related to project work, if written Test

Examination

conducted

J

Place of Work

ICMR Hqrs.

K

Date & Time of

23th

February, 2018 strictly between 09:00 A.M to 10:00

Written Test/

A.M

Interview

S.NO.

Details

Requirements/Information

1.

A

Name of Posts

Consultant (Scientific) Biomedical Research

B

No. of Vacancies

One Posts

C

Essential Qualification

Post Graduate Degree (MD/MS/DNB) after MBBS

with one year clinical experience

OR

Postgraduate diploma after MBBS with 2 years clinical

experience with the recognised government institution

OR

MBBS with four year clinical experience in

Government Institution

D

Desirable

I.Knowledge of writing clinical trials protocols

and regulatory submissions.

II.

Able to prepare standard operating Procedures

for the trial conduct.

III.

Should possess administrative skills for

managing the clinical research.

E

Age

Limited as on date: up to 70 years

F

Nature of Duties

Develop the quality biomedical research documents

and support research training, , development of

research infrastructure, and facilitate collaboration

(including with clinical research)

Promote biomedical research activities.

Oversee and review biomedical research

performance and research integrity

G

Consolidated

Maximum Rs.70,000/- per month depending upon

Emoluments

experience and knowledge.

H

Tenure

Two Years

I

Syllabus for Written

Degree level related to project work, if written Test

Examination

conducted

J

Place of Work

ICMR Hqrs.

K

Date & Time of

24th

February, 2018 strictly between 09:00 A.M to 10:00

Written Test/

A.M

Interview

Post of Consultants (Scientific) Biomedical Research

Quality Assurance 1 positions

S.NO.

Details

Requirements/Information

1.

A

Name of Posts

Consultant (Scientific) Biomedical Research Quality

Assurance

B

No. of Vacancies

One Posts

C

Essential Qualification

Post Graduate Degree (MD/MS/DNB) after MBBS

with one year clinical experience

OR

Postgraduate diploma after MBBS with 2 years clinical

experience with the recognised government institution

OR

MBBS with four year clinical experience in

Government Institution

OR

Ist class Masters in Medical Pharmacology/Medical

Microbiology with 4-6 years experience in clinical

trials/studies.

D

Desirable

Experience in evaluating quality events, incidents,

queries and complaints and handling compliance

issues.

Experience

in

managing and maintaining

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

Age

Limited as on date: up to 70 years

F

Nature of Duties

Ensure that all processes contributing to the

performance of a clinical trial are conducted

properly.

Troubleshoot clinical trials and activities.

Prepare and assist in preparing annual reports and

quality trending reports.

Report the status of the quality levels of the staff,

systems and production activities.

Preside over improvement programmes.

Keep upto date with all quality and compliance

issues.

G

Consolidated

Maximum Rs.70,000/- per month depending upon

Emoluments

experience and

knowledge.

H

Tenure

Two Years

I

Syllabus for Written

Degree level related to project work, if written Test

Examination

conducted

J

Place of Work

ICMR Hqrs.

K

Date & Time of

24th February, 2018 strictly between 09:00 A.M to 10:00

Written Test/

A.M

Interview

S.NO.

Details

Requirements/Information

1.

A

Name of Posts

Consultant (Clinical Coordinator) (Medical)

B

No. of Vacancies

One Post

C

Essential Qualification

Post graduate Degree (MD/MS/DNB) after MBBS

with 1 year experience

OR

Post graduate Diploma in Medical subject after MBBS

with 2 year experience

OR

MBBS with 4 year clinical/research experience in

Govt. Institution.

OR

Ist class Masters in Medical Pharmacology/Medical

Microbiology with 4-6 years experience in clinical

trials/studies.

D

Desirable Experience

Able to prepare SOPs for trial conduct.

Thorough knowledge of GCP, ICH guidelines and

regulatory requirements for clinical trial conduct.

Experience in co-ordinating project activities

Good communication skills

E

Age

Limited as on date: up to 70 years

F

Nature of Duties

Coordination of project activities and

Implementation at all sites.

Communication to International and National

agencies.

Preparation of financial documents, Data

Programme Report, Report writing.

Drafting letters for sending to various

organizations.

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.

G

Consolidated

Maximum Rs.70,000/- per month depending upon

Emoluments

experience and knowledge.

H

Tenure

Two Years

I

Syllabus for Written

Degree level related to project work, if written Test

Examination

conducted

J

Place of Work

ICMR Hqrs.

K

Date & Time of

24th February, 2018 strictly between 09:00 A.M to 10:00

Written Test/

A.M

Interview

S.NO.

Details

Requirements/Information

1.

A

Name of Posts

Consultant (Scientific) Clinical Development

B

No. of Vacancies

One Post

C

Essential Qualification

Post Graduate Degree (MD/MS/DNB) after MBBS with one

year clinical experience

OR

Postgraduate diploma after MBBS with 2 years clinical

experience with the recognised government institution OR

MBBS with four year clinical experience in Government

Institution

OR

Ist class Masters in Medical Pharmacology/Public health from a

recognized University with 4 years of experience in Pharma

industry/CRO industry/Bio-tech industry /Public Health

D

Desirable Experience

PhD in relevant subject from a recognized University

Experience in biomedical research preferably in TB or other

infectious disease

Good scientific writing/Communication skills.

Knowledge of computer applications or business intelligence tools

management/ data synthesis.

E

Age

Limited as on date: up to 60 years

F

Nature of Duties

Study feasibility, site feasibility, site identification (with CRPs) and

site selection - Clinical studies and Observational Research

Deliver all regional, local, and corporate portfolio

commitments/milestones for sites and trials within responsibility

Support local needs of globally outsourced studies within

responsibility

Manage IITs

Regulatory submissions, in affiliates which are managed by

Clinical Operations

Manage the allocation of patients within the geography

Manage Site enrolment performance

Assist sites in recruitment planning

Develop site level risk plan for enrolment

Primary interface with investigators

Manage the link between site and the TPO

Collaborate with partners and other study team members to

resolve/escalate site specific issues when necessary

Contribute to and partner with the local medical organization to

deliver on department goals .

The job may require travel to the trial sites and attending

outstation meetings

G

Consolidated

Maximum Rs.70,000/- per month depending upon experience

Emoluments

and knowledge.

H

Tenure

Two Years

I

Syllabus for Written Test

Degree level related to project work, if written Test conducted

J

Place of Work

ICMR Hqrs.,

K

Date & Time of Written

24rd February,2018 strictly between 09:00 A.M to 10:00 A.M

Test/ Interview

S.NO.

Details

Requirements/Information

1.

A

Name of Posts

Consultant (Scientific) Clinical Operations

B

No. of Vacancies

One Post

C

Essential Qualification

Post Graduate Degree (MD/MS/DNB) after MBBS with one

year clinical experience

OR

Postgraduate diploma after MBBS with 2 years clinical

experience with the recognised government institution OR

MBBS with four year clinical experience in Government

Institution

OR

1st Class Masters Degree in Medical Pharmacology/ Public Health

from a recognized University with 4-6 years of experience in

Pharma/Biotech/CRO industry/ Public Health related to clinical

research / trails.

D

Desirable

PhD in Microbiology, Pharmacology/ Public Health from a

recognized University

Experience in managing clinical trials of drugs and vaccines for

regulatory submission

Able to prepare standard operating Procedures for the trial

conduct.

Knowledge of GCP, ICH guidelines and regulatory requirements

for clinical trials conduct.

E

Age

Limited as on date: up to 70 years

F

Nature of Duties

To manage all clinical aspects of study including assessing

operational feasibility and recommending study execution plan;

developing and managing comprehensive study timelines and

metrics

To participate in Selection and management/Oversight of external

vendors and develops vendor specifications; review vendor

reports, budgets and metrics

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 specific meetings

To participate in Site monitoring visits and oversee clinical

monitoring 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

Any other work assigned by the team leader pertaining to ITRC

The job may require travel to the trial sites and attending

outstation meetings

G

Consolidated

Maximum Rs.70,000/- per month depending upon experience

Emoluments

and knowledge.

H

Tenure

Two Years

I

Syllabus for Written

Degree level related to project work, if written Test conducted

Examination

J

Place of Work

ICMR Hqrs.

K

Date & Time of Written

24 February 2018 strictly between 09:00 A.M to 10:00 A.M

Test/ Interview

9

S.NO.

Details

Requirements/Information

1

A

Name of Posts

Consultant (Scientific) Pre-Clinical operations

B

No. of Vacancies

One Post

C

Essential Qualification

Post Graduate Degree (MD/MS/DNB) after MBBS with one year

clinical experience

OR

Postgraduate diploma after MBBS with 2 years clinical experience

with the recognised government institution OR

MBBS with four year clinical experience in Government

Institution.

OR

1st Class Masters Degree in Medical Microbiology/ Medical

Pharmacology/Immunology from a recognized University with 4-6 years

of experience in Pharma industry/Biotech industry /CRO industry /

Immunology related to clinical research studies / trials.

D

Desirable

PhD in Medical pharmacology/medical microbiology/immunology

from a recognized University

Strong knowledge of clinical research process and medical

terminology.

Understanding of GCP/ICH guidelines.

Knowledge of regulatory requirements and guidelines governing

clinical research.

Ability to work successfully within a cross-

functional team

Good Scientific writing/Communication skills Knowledge of

computer applications or business intelligence tools/data

management / data synthesis

E

Age

Limited as on date: up to 70 years

F

Nature of Duties

To manage all clinical aspects of study including assessing operational

feasibility and recommending study execution plan; developing and

managing comprehensive study timelines and metrics

To participate in Selection and management/Oversight of external

vendors and develops vendor specifications; review vendor reports,

budgets and metrics

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 specific meetings

To participate in Site monitoring visits and oversee clinical monitoring

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

The job may require travel to the trial sites and attending outstation

meetings

G

Consolidated

Maximum Rs.70,000/- per month depending upon experience and

Emoluments

knowledge.

H

Tenure

Two Years

I

Syllabus for Written Test

Degree level related to project work, if written Test conducted

J

Place of Work

ICMR Hqrs.

K

Date & Time of Written

24 February 2018 strictly between 09:00 A.M to 10:00 A.M

Test/ Interview