The Indian Council of Medical Research (ICMR), of the Department of Health Research (DHR), New Delhi, the apex body in India for the formulation, coordination and promotion of biomedical research, is one of the oldest medical research bodies in the world.

The Primary objective of Tata Trusts is to impact the quality of life of the community. Tata Trusts have been working on a range of thematic areas cutting across diverse developmental issues like Health, Education, Media & Arts, Natural Resources & Livelihoods and Urban Poverty.

The Govt. of India through Indian Council of Medical Research (ICMR) has setup an “Indian TB Research Consortium (ITRC)” 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 in accelerating the development of new diagnostics, new & improved vaccines and Immunotherapies, drugs for TB.

Consultant Medical Writer
Essential Qualifications :
• 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 or equivalent with 2 years* of demonstrated experience in clinical research/trial OR
• Ist class Masters (MSc/ M.Pharma) in medical Pharmocology/Biotechnology/ClinicalResearch/Microbiology/Bioche mistry with 4-6 years* demonstrated experience in clinical research/trial

Desirable :
• Demonstrated Experience in regulatory writing as a part of pharmaceutical or CRO industry
• Significant knowledge of global , national and other clinical development guidelines
• Excellent computer skills and relevant applications

Age : Not exceeding 50 years

Nature of duties :
• Independently research, write and edit peri/ post –approval clinical study reports, study protocols and standard response documents.
• Provide high quality medical and scientific writing from planning and conduct of literature search through editing of final drafts.
• Contributing to a variety of documents for clinical research and regulatory purposes, including clinical research protocols, annual and final study reports , investigator’s brochures and regulatory submissions including clinical summary reports(CSR), clinical evaluations(CER) and post market surveillance (PMS) reports
• Produce complex clinical or scientific documents such as manuscripts, posters, abstracts, oral presentation slide decks, review articles and dossier.
• Provide senior review of documents and training/ mentoring for other writers.
• Manages all aspects of planning , organizing and executing projects without supervision including : developing project timelines, standards, budgets, forecasts and contract modifications
• Liaises with other functional units as necessary.
• Any other work that may be assigned from time to time by the concerned ICMRofficials.
• The job may require travel to the trial sites and attending outstationmeetings

Consolidated Emoluments : UptoRs. 70,000/- per month**

Tenure : One year

Syllabus for written examination : Degree level related to project work, if Written Test conducted

Consultant (Clinical Coordinator)
Essential Qualifications :
• Post Graduate Degree (MD/MS/DNB) with one year* of demonstrated experience of clinicalresearch /Trial OR
• Post Graduate Diploma in clinical research after MBBS /BAMS or equivalent with 2years* of demonstrated experience in clinical research/ trial OR
• Ist class Masters (MSc/ M.Pharma) in medical Pharmacology/Biotechnology/Clinical Research/Microbiology/Biochemistry with 4-6 years* demonstrated experience in clinical research/ trial of which one year should be in TB research

Desirable :
• Able to prepare SOPs and related documents for clinical trial conduct.
• Thorough knowledge and understanding of ICH GCP guidelines and relevant regulatory requirementsfor clinical trial conduct.
• Experience in co-coordinating projectactivities
• Good communicationskills

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 Nationalagencies. 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 asrequired.
• Trial Data review and checks for accuracy and adequacy
• Any other work that may be assigned from time to time by the concerned ICMRofficials.
• The job may require travel to the trial sites and attending outstationmeetings.
• Preparation of financial documents, Data Programme Report, Reportwriting
• Drafting letters for sending to various organizations

Consolidated Emoluments : Upto Rs.50,000/- per month **

Tenure : One year

Syllabus for written examination : Degree level related to project work, if written Test conducted

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Consultant (Scientific)
Essential Qualifications :
• 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 or equivalent with 2 years* of demonstrated experience in clinical research/trial OR
• Ist class Masters (MSc/ M.Pharma) in medical Pharmocology/Biotechnology/ClinicalResearch/Microbiology/Bioche mistry with 4-6 years* demonstrated experience in clinical research/trial
• Should possess administrative skills for managing the clinical research.

Desirable :
MD/ or PhD with clinical Research experience in the relevant areapreferably from a Government Institute
i. Good Scientific writing/Communication skills.
ii. Knowledge of computer applications or business intelligence tools/data management / data synthesis

Age : Not exceeding 60 years

Nature of duties :
• Coordination of project activities and Implementation at all sites. Travel to trial sites for assessment and monitoring.
• To work under team leader and complete the specialized tasks assigned in the related area of work in time.
• Literature review and preparation of study protocols for TB related clinical trials. Preparing amendment for protocol and related documents
• Coordinating with Regulatory team for and making study protocol presentation to DCGI office
• Preparing and Convening Investigators meetings for finalization of protocols
• Organizing & co-coordinating protocol review meets whenever required by ITRC.
• Coordinating with other divisions of ICMR for getting inputs related to various issues like IPR etc.
• Preparation of various protocol related documents as per WHO and DCGI guidelines
• Preparing Clinical data management plan, design CRF and organize training of the project staff for the electronic data entry.
• Writing scientific papers for publications in various journals
• Any task/ duty assigned by the Programme officer.
• The job may require frequent travel to sites for quality assurance check and quality management.

Consolidated Emoluments : UptoRs. 90000/- (consolidated) per month**

Tenure : One year

Syllabus for written examination : Degree level related to project work, if Written Test conducted

Notes: PhD in relevant subject shall be treated equivalent to three years of experience. *Selection committee may relax in experience in criteria with exceptionally good candidatepossessing essential qualifications
** Salary will be decided depending upon the experience and suitability of the candidate.

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Selection Procedure: Interview will be conducted for the eligible candidates. However, if more number of candidates are found eligible for the post advertised, Written Test/ Skill Test may also be conducted on the same day before final round of Interview.

The candidates should bring 6 copies of biodata along with all original certificates of educational qualifications (from SSC onwards), experience, Aadhaar Card, with one set of photocopies of the same duly attested (can be self attested) along with a passport size photograph for attending the Written Test/Interview. No TA/DA will be paid for attending the Written Test/ Interview. The recruited project staff is eligible for leave as per rules and will have to give an undertaking before joining.

Interested candidates for the positions mentioned below are invited to appear for the walk-in interview along with 6 copies of their applications in prescribed format (Annexure 1) with one photograph on 14th Februray 2019 between 9:00 am to 10:00 am(as mentioned against the respective posts below) at Indian Council of Medical Research Ansari Nagar New Delhi 110029.

The candidates can also submit their CV strictly the prescribed format attached before at teamtbconsortium@gmail.com;vadehra.icmr@gmail.com However the candidate should report for interview at 9.00AM for appearing for the interview on the date mentioned above in person for application/CV to be considered in interview. Latecomers will not be entertained after 11:00 A.M. under any circumstances.

GENERAL CONDITIONS:
The conditions for employment will be the same as that of the project staff on contract basis. The candidates have no right to claim for any regular employment at this Institute. The appointing authority has the right to accept/ reject 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 test/ Interview.

Note: No electronic device including Calculator and Mobile phones would be allowed in the examination Hall.