Job Openings for Pharmacy Consultants in ICMR | Salary upto Rs 90,000/- pm

 

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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