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Job Openings for Ph.D, M.Pharm as Consultant under Division of ECD at ICMR | Salary Rs 1 lakh pm

 

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 medical research bodies in the world.

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

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

For TB Vaccine Trial

Consultant (Senior Protect Manager)

No. of post : One Post

Essential Qualifications
Post Graduate Degree (MD/MS/DNB/Ph.D) after MBBS with four years of demonstrated core experience after postgraduation in Vaccine/drug trial from reputed Institution/CRO.
OR
MBBS or equivalent with 8 years of demonstrated core experience in managing regulatory Vaccine/drug trial/ from reputed Institution/CRO.
OR
1st class Masters degree M. Pharma/ or M.Sc in Pharmacology/ Biotechnology/life sciences with 8 years of demonstrated core experience in managing / monitoring regulatory Vaccine / drug trial from reputed Institution/CRO

Desirable
• Experience in conducting Vaccine/drug trial/clinical research.
• Experience in establishing clinical trial sites, management &
implementation of trials and managing and maintaining databases for quality systems.
• Able to prepare & review SOPs and logs relevant requirement for trial sites
• Thorough knowledge of new clinical trial rules, Schedule Y, GCP, GCLP, ICH guidelines and regulatory requirements for conduct of clinical trial.
• Good communication skill

Age Limited as on date : up to 70 years

Nature of duties  
 • Establish and ensure that all processes for conduct of vaccine trials, CRFs, data management etc. are in place for ensuring expected performance.
• Prepare detailed project management plan and safety management plan and ensure execution as per plan.Prepare data management plan with data manager and ensure preparation of statistical analysis plan with help of statistician.
• Communicate with sites for ensuring smooth conduct and provide support as and when required.
• Co-ordinate with monitoring team for study compliance and study management/monitoring and obtain weekly updated reports from team.
• Submit updated site specific and consolidated progress report to Team leader/ Programme officer every week
• Troubleshoot with all sites for smooth conduct of vaccine trial.
• Prepare SAE management plan and Prepare and assist in preparing adverse event / serious adverse event narratives, safety reports, progress reports and quality trending reports.
• Will be responsible for site initiation and site management, monitoring timely reports of adverse event / serious adverse event by site Pis and communication with regulators.
• Report the status of the quality levels of the staff, systems and production activities.
• Keep upto date with all quality and compliance issues.
• Prepare interim and final Clinical report as per guidelines.
• Prepare relevant documents (note to files, protocol deviations etc.) and ensure timely submission to sponsor, IECs and Regulators.
• The job requires frequent All India travel to sites for monitoring, quality assurance and quality management.
• Ensuring operational approach of the vaccine trial are in place
• Any other duty assigned by the PI or Programme officer.

Consolidated Emoluments : Rs. 1,00,000/- per month depending upon experience and knowledge.

Tenure : Initial for one year and may continue upto three Years

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

Place of work : ICMR/DHR Hqrs., New Delhi

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For Project ‘India TB Research Consortium’

Consultant (Scientific) Clinical Coordinator

No. of post : One Post

Essential
Post Graduate Degree (MD/MS/DNB/Ph.D) after MBBS with one year of demonstrated experience in clinical research/Biomedical Research from reputed Institutions.
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
lstclass Masters in M.Pharma , M.Sc in Pharmacology/Medical Microbiology / Biochemistry/ Biotechnology with 4 years of demonstrated experience in clinical research/ /Biomedical Research from reputed Institution.
OR
2nd class Masters in M. Pharma , M.Sc in Pharmacology/Medical Microbiology/ Biochemistry/Biotechnology/ Clinical Research with Ph.D in any of the above disciplines with 2 years post Ph.D demonstrated experience of clinical research/trial.

Desirable
• Experience in conducting Vaccine/drug trial/clinical research/ /Biomedical Research.
• Experience in managing and maintaining databases for quality systems.
• Knowledge of preparation of the protocol and budget for studies.
• Update the landscape documents in all thematic areas of TB
• Able to prepare SOPs for trial conduct.
• Thorough knowledge of GCP, ICH guidelines and regulatory requirements for clinical trial conduct.
• Good communication skills

Age Limited as on date : up to 70 years

Nature of duties  
• 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 as per the ITRC SOPs and consolidate the information pertaining to all the projects and activities undertaken or proposed to be undertaken under ITRC and would be responsible for finishing the assigned tasks on time.
• Troubleshoot clinical trials and multi-centric projects.
• 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.
• To organize meetings, take care of logistics and administrative and financial approvals, draft letters for sending to various organizations and prepare the draft minutes of the meeting
• Keep upto date with all quality and compliance issues.
• Process matters for sanction of the projects as recommended y expert groups of ITRC, take follow-up actions till release of budget.
• To obtain the updated progress reports from sites and also consolidated reports from the project co-ordinators and regular y submit to ITRC Program officer
• To work in team and undertake and share the responsibilities as and when required with other ITRC staff.
• The job may require frequent All India travel to sites for monitoring, quality assurance and quality management.
• Any other job assigned by the PI or Programme officer

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

Tenure :  one year

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

Place of work : ICMR/DHR Hqrs., New Delhi

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SELECTION PROCEDURE:
Interview will be conducted to 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 of educational qualifications (from SSC onwards), experience, Aadhaar Card, Community Certificates (For reserved post) along with two sets 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 appointment is purely on contractual basis. 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 for any regular employment at this institute.

The appointing authority has the right to accept/ reject any application without assigning any rcason(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       

Interested candidates for the various positions mentioned below are invited to appear for the Walk-in interview/Written Test along with 5 copies of their updated Bio data CV (as per enclosed format) on 8th August 2019 between 09:00 A.M to 11:00 A.M at Indian Council of Medical Research, Ansari Nagar, New Delhi-110 029. The Biodatas may be sent via e-mail at teamtbconsortium@gmail.com

Late comers will not be entertained beyond 11.00 AM under any circumstances.

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