www.icar.org.in Recruitment 2012 Central Avian Research Institute : Personal Assistant
Name of the organisation : Central Avian Research Institute ( icar.org.in ) Name of the post : Recruitment for Personal Assistant in 2012
Director, CARI, Izatnagar invites applications from the eligible candidate for filling up the post of Personal Assistant (Unreserved) at CARI, Izatnagar under the Administrative Control of ICAR. The post is of permanent nature and at present is filled on temporary basis. The appointee will be made permanent subject to satisfactory performance during the probationary period.
Personal Assistant - One post
Pay Band + Grade Pay : 9300-34800 Plus Grade Pay 4200
Educational & other qualification required for direct recruitment : Matriculation or its equivalent examination.
Professional Efficiency :
The candidate will be given one dictation test in English or in Hindi at 100 w.p.m. for 10 minutes. The candidates who opt to take the test in English will be required to transcribe the matter in 50 minutes on manual typewriter or 40 minutes on computer and the candidates who opt to take the test in Hindi will be required to transcribe the matter in 65 minutes on manual typewriter or 55 minutes on computer.
Age limit for direct recruitment :
18-27 years (the upper age is relaxable for SC/ST/OBC as per the Govt. of India rules. The upper age is also relaxable upto 45 years in the case of serving regular employees of ICAR in the administrative (Ministerial) category.
Application may be made on plain paper strictly typed/hand written in the prescribed format containing particulars/ information duly supported by attested copies of educational / technical/Caste experience certificate etc. The applications complete in all respects, should reach the Director, Central Avian Research Institute,Izatnagar - 243 122 within 30 days from the date of publication of this advertisement along with a demand draft for Rs. 200/- drawn in favour of CAR unit CARI payable at Bareilly. No fees for SC/ST candidates.
Applicants should have registered their names in Employment Exchange, otherwise their applications will not be considered.
Applications received after the due date for whatsoever the reason including postal delays will not be entertained.
Incomplete Applications and/or Application not signed by the candidate will be rejected out rightly.
Last edited by mariammal; January 21st, 2012 at 12:52 PM.
Name : natesh babu Email : nattiforu AT gmail.com Designation / Skillset : CRA, clinical research associate , all clinical operations
Dear sir/ Madam
I was excited to read about Clinical Research Associate job opening at your company
I have a Bachelors degree Medical Laboratory from St. Johns Medical College Bangalore and also MSC
in clinical research ICRI Bangalore with one years experience in clinical operations. I have 5months
experience as a CRC Manipal Hospital Banaglore and also six months experience CRA Trainee Allergan
India Pvt Ltd Bangalore where I was working in a medical setting with a wide range of experience of
tasks and responsibilities focusing on assisting clinical studies.
In an addition to my extensive experience, I completed my Diploma in ADSE computer course which I
found highly interesting and this has motivated me to apply for this position.
I am a hardworking person who enjoys a challenge both as part of a team and as an individual.
Thank you for your consideration. I look forward to hearing from you to arrange an interview.
If you need to contact me in the meantime, I shall also be available on mobile number
Sincerely,
Natesh Babu K
Resume :
Curriculum Vitae CAREER OBJECTIVE :
Aim to work in an organization where I can prove, improve and update my knowledge and skills
in accordance with the latest trends and to be part of a team that dynamically works towards growth of the
organization. SKILLS :
Flexible and ability to learn quickly.
Helpful in facilitating team with problem solving abilities.
Enthusiastic towards learning new things.
Committed to deadlines and work schedules.
EDUCATIONAL QUALIFICATION :
Master of Science in Clinical Research (64%) from Institute of Clinical Research of India (ICRI)
Bangalore, Cranfield University, UK, 2008-10 (August).
Post Graduate Diploma in Clinical Research Management from ICRI Bangalore, 2008-2009.
Bachelor in Medical Laboratory Technology (70%) from St John ’s Medical College Bangalore,
Rajiv Gandhi university health & Science, 2004-2008.
Intermediate in Medical Laboratory Technology (85%) from Sri Balaji Vocational College,
Madanapalli, Chittoor AP, Board of Inter Mediate examination, 2002-2004.
SSLC (56%) from Gnanodaya Publish School, Madanapalli, Chittoor, AP Board of secondary
examination 1997. CERTIFICATIONS :
- GCP training by Pfizer and Manipal Hospital Clinical Research Center Bangalore. COMPUTER PROFICIENCY :
PG.Diploma in ADSE
Internet Applications
PROFESSIONAL EXPERIENCE :
v I have worked as a CRC in Manipal Hospital Bangalore Clinical research from September 2010
to December2010.
Role and responsibility
- Preparation and subsequent submission of study related documents to the Ethics committee for
approval.
- Extensive experience in counseling and recruitment of patients.
- Coordinating between the site and sponsor/CRO and all activities related to the study within the site.
- Ensuring that study is going as per ICH & GCP guidelines and also the study protocol, SOP and other
regulatory requirements.
- Maintenance of trial master files (patient screening log, patient enrollment log, drug accountability
log, etc.).
Filling the case report form [CRF/e-CRF (electronic)] by using source document and query
-
Management.
- Randomization of patients (through IVRS).
- Reporting the SAE to ethical committee and the sponsor
- Filling sample requisition forms of the patient.
Shipping of samples to International and Local labs.
-
- Executes other duties as may be assigned by the Clinical Operations Management/delegate as training
and experience allow.
Conducting Ethics Committee Meetings and handling Feasibility documents.
v I am working as a Clinical Research Associate Trainee in Allergan India Pvt Ltd, Bangalore
from Jan 2011 to till date.
Role and responsibility
Selection of site and investigator (feasibility).
Coordinating with the site for receiving investigators undertaking and agreement.
Submission of documents to both central and institutional ethics committee for approval of site for
conduct of the trial.
Coordinating with site for availability of site personnel and investigator for conduct of site initiation
visit.
-
Training site personnel with protocol, ICH GCP and procedure for obtaining Informed consent and
filling case report form
-
Coordinate with site for details of patient enrollment
Conduct routine monitoring visit during patient enrollment.
Conduct of source document verification.
Updating Trial master file.
-
Coordinate with site for adverse event reporting.
-
Conduct of close out visit.
-
-
Retrieval of filled case report form and informed consent form.
Retrieval of used and unused study samples.
-
-
Responsible for destruction of study samples.
-
Payment to investigator for conduct of trial according to financial report. PROJECTS UNDERTAKEN : Project 1 :
Title : Study of prevalence of asthma in hand loom weavers in Madanapalli Town ,
Chitoordistrict, A.P Sample size : 200
Subject : Epidemiological study.
Unit : Madanapalli,
Duration : 2 months
Year : 2009 Project 2 :
Title : Educational interventional study on tuberculosis among general population in
Madanapalli. Sample size : 300
Subject : Educational interventional study
Unit : Madanapalli
Duration : 4 months
Year : 2010
DECLARATION:
I hereby declare that the above mentioned information is correct up to my knowledge and I bear the
responsibility for the correctness of the above-mentioned particulars.
Yours truly,
Natesh Babu.K
Bangalore
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More Information about this submission and submitter:-
___________________________________________________
Submission ID : 4370376
Date & Time : 14th Jul 2011 11:11 AM (UTC)
IP Address : 110.234.118.174
Browser Info : Mozilla/5.0 (Windows NT 5.1) AppleWebKit/534.30 (KHTML, like Gecko) Chrome/12.0.742.122 Safari/534.30
Predicted Country : Australia
Last edited by Guest-IJT; December 2nd, 2011 at 10:32 AM.
post graduate in food processing with qualification in food science and quality control
RESUME
MAREENA JOSEPH Email : mareenajoseph90 AT yahoo.com
CAREER OBJECTIVE :
Quest to work in a very competitive professional environment that gives a scope for learning the latest and emerging technologies. I aspire to help a growth oriented organisation, to reach its target with sincerity of purpose and determination to succeed. PERSONAL ATTRIBUTES :
- Confident to work independently and as a team member.
- Excellent communication skills.
- Strong computer & Internet skills
- Well-Motivated and hard working.
- Quickly adjustable to any type of environment. EDUCATIONAL QUALIFICATION :
Presently Persuing M.Sc Food processing.
Academic Profile
Exam Passed Board / University Year Of Passing % of Marks
M.Sc, Food Processing
(!st Semester) Periyar University
Salem Still Continuing 81
B.Sc. Food Science & Quality Control Mahatma Gandhi University, Kottayam 2010 89
X11th State Board of Secondary Education 2007 74
Xth State Board of Secondary Education 2005 79 TECHNICAL QUALIFICATIONS :
- WINDOWS 98 / 2000 / XP
- MS – Office (Word, Excel, Powerpoint) AVAILABILITY :
Ready to accept immediate assignment on 30 days notice
WORK EXPERIENCE
1. IN – PLANT TRAINING
1. One month training in meat products of India (MPI), Edayar, Koothattukulam.
2. One month training in malana dairy LTD.kerala
PROJECT WORK
Industry : Nestle India LTD Topic : effect of starch damage and viscosity on the wafer quality Duration : One Month
HOBBIES
Reading books, Cooking, Listening Music’s.