Job Openings for Pharmacy professionals (9 posts) to work in ICMR as Consultant | Salary upto Rs 1 lakh per month

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Consultant (Scientific) Clinical Coordinator

Essential Qualifications :
Post Graduate Degree (MD/MS/DNB/Ph.D) afters 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/ Biochemistry/ Biotechnology with 4 years of demonstrated Experience  in clinical research /Biomedical Research from reputed Institution
OR
2nd class masters in M.Pharm, 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..
• Able to prepare SOPs, project management plan and study monitoring plan for trial conduct.
Thorough knowledge of GCP, GCLP, ICH guidelines and regulatory requirements  for conduct of clinical trial.
• 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 conductedproperlyas 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 by 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 regularly 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, New Delhi

 

Consultant (Scientific) Clinical Development

Essential Qualifications :
Post Graduate Degree (MD/MS/DNB/Ph.D) afters 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/ Biochemistry/ Biotechnology with 4 years of demonstrated Experience  in clinical research /Biomedical Research from reputed Institution
OR
2nd class masters in M.Pharm , 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  clinical research/Biomedical Research.
• Experience in managing and maintaining databases for quality systems..
Have medical writing skills for writing protocols/ clinical study reports/ prepare CRFs, proforma etc
• Able to prepare SOPs, project management plan and study monitoring plan for trial conduct.
Thorough knowledge of GCP, GCLP, ICH guidelines and regulatory requirements  for conduct of clinical trial.
• Good communication skills

Age Limited as on date : up to 70 years

Nature of duties
• Work as per the ITRC SOPs and undertake new project clinical trial development plan.
• 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 new 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 aclinical 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.
• Keep upto date with all quality and compliance issues.
• The job may require frequent All India travel to sites for monitoring, quality.
• 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, New Delhi

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