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Job for M.Pharm as Consultant in Clinical Development at ICMR - Salary Rs 70,000/- per month

 

Clinical courses

 

Clinical courses

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

Indian Council of Medical Research (ICMR) has initiated various projects for development of new tools and implementation strategies to support Govt, of India under TB Elimination Goa by 2025.

Post : Consultant (Scientific) Clinical Development

Following posts are to be filled purely on contractual basis for working under various Flagship programme under Division of Epidemiology and Communicable Diseases (ECD-I), ICMR Hqrs. Office, New Delhi.

Essential Qualification & Minimum Experience required
Post Graduate Degree (MD/MS/DNB/Ph.D) after MBBS with one year of demonstrated experience in clinical research /Biomedical Research from reputed Institution.
OR
MBBS or equivalent with four year of clinical experience in Government Institution of which 2 years should be demonstrated experience in clinical research /Biomedical Research from reputed Institution.
OR
1st class Masters in M. Pharma, M.Sc in Pharmacology/Medical Microbiology / Biotechnology with 4 years of demonstrated experience in clinical research/ Biomedical Research from reputed Institution.
OR
1st class Masters in M. Pharma, M.Sc in Pharmacology/Medical Vlicrobiology / Biotechnology with Ph.D in any of these subjects with 2 years of demonstrated experience in clinical research/ Biomedical Research from reputed Institution.

Desirable
• Experience in conducting clinical research Biomedical Research.
• Experience in literature search, publications
• Have medical writing skills for writing protocols/ clinical study reports/ prepare CRFs, proforma etc.
• Able to prepare SOPs for clinical trial conduct.
• Thorough knowledge of GCP, GCLP, ICI I guidelines and regulatory requirements for clinical trial.
• Good communication skills

Age Limited as on date : up to 60 years

Nature of duties
• Work as per the ITRC SOPs and undertake new project clinical trial development plan.
• Drafting of new study protocols/proposals/study reports/ notc/publications in journals etc. or potential research in Tuberculosis
• Designing and providing inputs in clinical protocol development for various thematic (Vaccines, diagnostics, therapeutics, Implementation research) areas of TB research.
• Prepare the SOPs for the project/clinical trial under ITRC and ensuring the compliance with activity and the project targets.
• Prepare clinical trial plan with the pew leads/molecules and submit to the team lead with details in a time bound manner.
• Co-ordinate the activities of the India TB Research consortium
• Ensure that all processes contributing to the performance of a clinical trial are conducted properly.
• Prepare monthly status update report of the performance with targets set and achieved and submit to PO monthly.
• Prepare minutes of meetings and take follow-up actions
• Report the status of the quality levels of the staff, systems and production activities.
• The job may require frequent All India travel to study sites for related work, meetings.

Consolidated Emoluments : Rs. 70,000/- per month consolidated.

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Tenure Initially : 6 months. Could be extended

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

Place of work : ICMR/DHR, New Delhi

SELECTION PROCEDURE:
Interview will be conducted ol the eligible candidates. However, if more number of candidates 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 5 copies of biodata along with all original certificates ot educational qualifications (from SSC onwards), experience, Aadhaar Card, with five set of photocopies of the supportive documents duly attested (can be self-attested) along with a passport size photograph for attending the Written Test/ interview.

The appointment is purely on contractual basis. 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.

GENERAL CONDITIONS: The conditions of employment will be the same as that of the project staff on contract basis. The candidates have no right to claim lor 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. However the selection Committee reserves the right to reduce the experience in case of deserving candidates.

Note: No electronic device including Calculator and Mobile phones are allowed in the examination Hall

Date and time of Interview
26th September, 2019, 2019 at 12.00h onwards (reporting time: 9,00AM to 11.00AM) at ICMR HQ.

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