ESIC Karnataka ESI Hospital Recruitment 2012 www.esickar.gov.in : Part Time Specialist

[muthukalee]

Name of the organisation : ESIC Karnataka ESI Hospital (esickar.gov.in)
Name of the post : Recruitment for Part Time Specialist in 2012

WALK-I N-INTERVIEW FOR APPOINTMENT OF PART TIME SPECIALISTS

http://esickar.gov.in/result.htm
http://esickar.gov.in/Rectt-Part%20t...s-Feb%2712.pdf

Walk-in-interview for appointment of Part Time Specialist s on contract basis is called for to work in various ESI Hospitals in Karnataka as given below :-

ESI Hospital, Inidiranagar, Bangalore
Date of interview and venue :
Date : 21-02-2012 Time 11-00 AM to 5-00 PM
Venue :
Conference Hall,
Directorate of ESIS Med.
Services, 2nd Block, S. Nijalingappa, Road, Rajajinagar,
Bangalore-10
Contact No. 080-23324216
No. of vacant posts : 19

ESI Hospital, Belgaum
Date of interview and venue :
Date : 27-02-2012 Time 11-00 AM to 5-00 PM
Venue :
Conference Hall,
Medical Superintendent,
ESI Hospital, Ashoknagar, Shivajinagar,
Belgaum-
Contact No. 0831-2474369
No. of vacant posts : 6

ESI Hospital, Hubli & Dandeli
Date of interview and venue :
Date : 26-02-2012 Time 11-00 AM to 5-00 PM
Venue :
Conference Hall,
Medical Superintendent,
ESI Hospital, Karwar Road,
Hubli
Contact No. 0836-2303219
No. of vacant posts : 14

ESI Hospital, Mysore
Date of interview and venue :
Date : 02-03-2012 Time 11-00 AM to 5-00 PM
Venue :
Conference Hall,
Medical Superintendent,
ESI Hospital,
K.R.S. Road,
Mysore-570020
Contact No. 0821-2512473
No. of vacant posts : 5

ESI Hospital, Davanagere
Date of interview and venue :
Date : 05-03-2012 Time 11-00 AM to 5-00 PM
Venue :
Conference Hall,
Medical Superintendent,
ESI Hospital, Nittuvalli Exten.
Davanagere-577002
Contact No. 08192-2559963
No. of vacant posts : 4

ESI Hospital, Mangalore
Date of interview and venue :
Date : 17-03-2012 Time 11-00 AM to 5-00 PM
Venue :
Conference Hall,
Medical Superintendent,
ESI Hospital,
Kadri Shivabhag,
Mangalore-575002
Contact No. 0824-2218740
No. of vacant posts : 8

Qualification required :
1. A recognised graduate MBBS Degree included in schedule Part-I of Medical Council of India.
2. A recognised Post Graduate in Super-Speciality like, Endocrinology, Neuro Physician & Neuro Surgery
3. A recognised Post Graduate Degree MD / Diploma in the respective speciality

[Guest-IJT]

Name : deepthi yarlagadda
Email : deepthikodali AT gmail.com
Designation / Skillset : Clinical Research Associate
Dear Sir/Madam,
I am forwarding My CV for the openings available at your organization, I am actively seeking clinical research job and would like to express my interest. I hold 6 years of experience in clinical research and i have the ability to work in team as well as independent if needed. If my abilities meet the need of your organization I would greatly appreciate the opportunity to speak to you.
Look forward to your response.
Thanking you in anticipation,
Deepthi Yarlagadda

Resume :
- Working as a Clinical Research Associate in Maya Clinicals, Hyderabad, India from Dec 2009 – till date
- At presently working in Pulmonology trial.
- Worked as a Clinical Research Associate for Multicentric in Neurology trail
Responsibilities :
- Identification of potential Investigators in collaboration with the sponsor
- Preparing Ethics Committee dossier submissions.
- Source data verification
- Generating & Resolving queries
- Monitoring Investigational Product Accountability
- Collection of Essential Documents
- Preparing Regulatory Compliance review packages
- Administrative set up of sites
- Archiving relevant documents as per procedures
- Preparing monitoring reports in timely manner
- Facilitating effective communication between Investigational sites & the project team through written, oral and electronic contacts.
- Maintains clinical trial management systems effectively in order to ensure adequate communication to project team.
PROFESSIONAL EXPERIENCE AS A CRA AT ROXAANE RESEARCH LIMITED :
Worked as a Clinical Research Associate for 2 Multicentric clinical trials in Endocrinology and Opthmalogy at Roxaane Research limited, Chennai, India from May 2008 – Dec 2009
Responsibilities :
- Identification of potential Investigators in collaboration with the sponsor
- Preparing Ethics Committee dossier submissions.
- Source data verification
- Generating & Resolving queries
- Monitoring Investigational Product Accountability
- Collection of Essential Documents
- Preparing Regulatory Compliance review packages
- Administrative set up of sites
- Archiving relevant documents as per procedures
- Preparing monitoring reports in timely manner
- Facilitating effective communication between Investigational sites & the project team through written, oral and electronic contacts.
- Maintains clinical trial management systems effectively in order to ensure adequate communication to project team.
PROFESSIONAL EXPERIENCE AS A CRC AT CARE HOSPITAL :
Worked as a Clinical Research Coordinator for 10 Multinational and Multicentric clinical trials in Cardiology at CARE Hospital, Hyderabad, India from 24 Jan 2004 – 26th May 2008.
Responsibilities :
- Recruit subjects in coordination with multiple primary point-of-care physicians for Phase II and phase III randomized trials Annotate and complete CRF, source documents, and data query resolution with appropriate personnel.
- Administered informed consent, document processes as per ICH and GCP guidelines, obtain appropriate documentation, waivers.
- Serious Adverse Event reporting as per protocol requirements, IRB and DCGI guidelines to Sponsor and regulatory authorities.
- Analysis of the clinical lab reports in conjunction with investigator and escalating the medical queries to medical monitor if any.
- Coordinate scheduled visits, protocol based tests, laboratory evaluations.
- Responsible for query generation and query resolution arising during the database entry.
- Coordinate periodic reporting, permissions, requirements with study managers for IRB.
- Maintenance of essential documents for the study SMF, Study logs and Communications.
- Communicating deviations from the protocol, SOPs, GCP, and the applicable regulatory requirements to the investigator and taking appropriate action designed to prevent recurrence of the detected deviations.
Education Qualification :
- Bachelor Degree of Chemistry, Physics and Maths in May 2002, from Madhumalancha Degree College, Bodhan, Nizamabad (Dist), Andhra Pradesh.
Computer Skills :
- Diploma in Computer Application from 10 Mar 2000 to 10 Jun 2000
- Knowledge in SAS, Concepts of INTERNET, and WINDOWS MS-OFFICE.

Other Skills :
- Excellent communication skills and interpersonal skills
- Works cooperatively in group settings as well as independently.
Clinical Research Audits faced :
- Global Audit for Study in Acute Myocardial Infraction.
Clinical Excellence Program Certifications :
- Clinical Excellence Program -13th Feb 2006 (SIRO Clinpharm Pvt.Ltd), Hyderabad, India
- Clinical Excellence Program – 18th Feb 2006 (Pfizer Pharma Ltd), Hyderabad, India. (As a Part of Investigator Meeting)
- Clinical Excellence Program – 14th Jul 2006 (Avantis Pharma Ltd), Bangalore, India. (As a Part of Investigator Meeting)
- Completing the Human Participants Protection Education For Research Teams online course, Sponsored by the National Institutes of Health(NIH), on 01/Apr/2008

Deepthi Yarlagadda
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More Information about this submission and submitter :-
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Submission ID : 4225770
Date & Time : 8th Jun 2011 5:38 AM (UTC)
IP Address : 183.83.237.49
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[Guest]

When will you call for the pharmacist posts?