www.himachal.nic.in Department of Ayurveda HP Recruitment 2012 : Ayurvedic Medical Officer

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  1. Post Count Number #1
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    www.himachal.nic.in Department of Ayurveda HP Recruitment 2012 : Ayurvedic Medical Officer

    Name of the organisation : Department of Ayurveda Himachal Pradesh HP (himachal.nic.in)
    Name of the post : Recruitment for Ayurvedic Medical Officer in 2012

    DEPARTMENT OF AYURVEDA, HIMACHAL PRADESH RECRUITMENT OF AYURVEDIC MEDICAL OFFICERS ON BATCH WISE CONTRACT BASIS

    Careers Page : http://himachal.nic.in/vacancy/
    Detailed Advertisement : http://himachal.nic.in/vacancy/AMORe...nt2012_A1b.pdf

    No. of vacancies, Regular/contract : 78 Nos on batchwise contract basis.

    Designation of the post(s) to be filled up : Ayurvedic Medical Officers .

    Minimum Educational Qualification :
    i) Matric or equivalent recognized by H.P. Board/University.
    ii) Recognized degree in Ayurveda of not less than 05 years duration from a recognized University/Board established by law or institution recognized by the Central/State Govt. /CCIM.
    iii) Compulsory Rotatory Internship wherever required by the Central Council of Indian Medicine.

    Desirable Qualification :-
    Knowledge of customs/manner and dialects of H.P. and suitability for appointment in the peculiar conditions prevailing in the Pradesh

    Age limit : 45 Years and below as on 1.1.2012.

    Last date of submission of application : 11.4.2012

    Applications should be addressed to
    THE DIRECTOR OF AYURVEDA,
    BLOCK NO.26, SDA COMPLEX KASUMPATI
    SHIMLA-171009.
    Attached Files Attached Files
    Last edited by muthukalee; March 26th, 2012 at 03:30 PM.

  2. Post Count Number #2
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    Name : Dr. Preeti Ramteke
    Email : pretyz_03 AT yahoo.co.in
    Designation / Skillset : Sr. CRA(Lead CRA)

    Resume :
    Summary
    Currently working as Sr. Clinical Research Associate with Research Pharmaceutical Services( J & J).
    I have worked with Quintiles for 4 years.
    I have 1 year experience of handling a study as lead.
    I have significant experience in Acute Coronary Syndrome, early and advanced Parkinson’s Disease, Alzheimer’s Disease, Diabetes and Infectious Disease and have been monitoring sites participating in large global multicentre trials.
    Responsibilities have spanned a full duration of studies from start up to study close out and review. I have been managing studies as lead CRA. I am experienced in preparing for and handling Sponsor Audits, Internal Audits, Quality Management Visits, Site assessment visits, GCP Compliance visits.
    Following is the summary of Responsibilities :
    - Feasibilities
    - Initiation visits
    - Audits
    - Attendance to Investigator Meetings
    - Monitoring visits & SDV
    - Lead Activities
    - Delivery of GCP training’s
    - Closure visits
    - Submissions to Regulatory body
    - Collection of regulatory packages
    - Submissions to Ethics committees
    - Drug accountability
    - Site Selection visits
    - Management of SAEs
    - Negotiating contracts and budget
    Employment History
    Employer/From – To Current Roles & Responsibilities
    RPS- J&J Sr. Clinical research Associate
    Quintiles Research(India) Pvt. Ltd, Mumbai
    From 27-May 07 – April 2011 Sr. Clinical Research Associate 1(Lead CRA)
    - Review ongoing progress of the study, identity resolve issues, coordinate with the sponsors and the third parties, manage monitoring team members, performed quality visits at the sites form the study start up to Archivals.
    - Perform site selection, initiation, monitoring and close-out visits in accordance with contracted scope of work and good clinical practice.
    - Provide monitoring visits and site management for a variety of protocols, sites and therapeutic areas.
    - Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
    - Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues to Clinical Team Lead (CTL) and/or line manager.
    - Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment,
    - Case report form (CRF) completion and submission, and data query generation and resolution.
    - Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports and other required study documentation.
    - May provide assistance to more less experienced clinical staff
    Project Description
    Phase Global/Local Indication Responsibilities
    1. Phase 3 Global Multicentre study Cardiology : Acute Coronary Syndrome. Responsible form Site feasibilities till site Initiations(2007-2008)
    2. Phase 3 Global Multicentre study Cardiology : Percutenous Coronary Intervention Responsible form Site Initiations till Archival (2007 -2010)
    3. Phase 3 Global Multicentre study Cardiology : Percutenous Coronary Intervention Responsible form Site Initiations till Archival (2007 -2010)
    4. Phase 3 Global Multicentre study Neurology : Alzheimer’s disease Responsible form Site feasibilities till site Archival (2008 onwards). Lead CRA form 2010.
    5. Phase 3 Global Multicentre study Neurology : Early Parkinsonion Disease
    Responsible from Site Initiations till Archival.(2009 onwards)
    6. Phase 3 Global Multicentre study Neurology : Advanced Parkinsonion Disease Responsible from Site Initiations till Archival.(2009 Onwards)
    7. Phase 3 Global Multicentre study Neurology : Early Parkinsonion Disease
    Responsible from Site start up till Archival.(2010 onwards)
    8. Phase 3 Global Multicentre study Neurology : Advanced Parkinsonion Disease Responsible from Site start up till Archival.(2010 onwards)
    9. Phase 3 Global Multicentre study Infectious Disease Responsible form Start up period as Lead (CTL equivalent) (2010 onwards)
    10. Phase 3 Global Multicentre study Cardiology : Atrial Fibrillation Performed Re monitoring.
    Education and Qualification :
    Degree University Year of Passing Percentage/Grade
    1. Post Graduate Diploma in Contract Research Organization K.M.K College of pharmacy, Mumbai 2007 A Grade
    2. Bachelors in Ayurvedic Medicine and Surgery (B. A. M. S) R. A. Poddar Ayurvedic College and Hospital, Mumbai 2006 (Internship-2007) 67%
    3. HSSC Maharashtra State Board 2000 69%
    4. SSC Maharashtra State Board 1999 75%
    Project Achievements :
    - Received Customer Care Award for Alzheimer’s disease study.
    - Received Customer Care Award for Acute Coronary Syndrome Disease study
    - Received 2 awards for highest recruitment and for exceeding targets in Acute Coronary Syndrome and in Parkinson’s disease study.
    - Received several work worth doing awards for recruitment, contribution to assessment visits of trainee CRA’s, being a back up CRA and supporting team during Audits.
    - Had been a mentor for a new CRA.
    - Was invited as a Guest Lecturer for delivering a lecture on Clinical Trial Monitoring at CES College of pharmacy-Mumbai
    Key Strengths :
    Excellent Grasping ability.
    Effective Communications Skills.
    Solution oriented abilities.
    Problem solving abilities.
    Leadership abilities and teamwork.
    Readiness in accepting all challenges.
    IT Skills
    - In depth knowledge of Microsoft Project 98
    - PC skills
    - MS Words
    - Excel
    - Power Point
    - Lotus Notes
    - Microsoft Outlook
    - Hands on experience in using eDC systems

    Dr. Preeti Ramteke
    -------------------------------------------------------
    More Information about this submission and submitter :-
    ___________________________________________________
    Submission ID : 4266026
    Date & Time : 17th Jun 2011 11:25 AM (UTC)
    IP Address : 148.177.217.131
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    Predicted Country : United States