www.syncorp.in TECHNOLOGIES Pvt Ltd Bangalore : MBBS Clinical Research Coordinator

[Admin]

Company Name : SYNCORP TECHNOLOGIES (P) Ltd
Company Location : Bangalore
Designation (of vacancy) : Clinical Research Coordinator
Company E-mail ID : syncorporissa@gmail.com
Company Website : www.syncorp.in

Job Description, Candidate Profile, Company Profile, Company Address :
We are looking for MBBS graduates from eastern part of India (Kolkata,Bhubaneswar) to work in Clinical Research Field.Contact us www.syncorp.in Mob :-09861268508

ABOUT US :
About Company SYNCORP TECHNOLOGIES (P) Ltd is a global provider of Clinical Research ,IVRS, Home Appliances and BPO services to the pharmaceutical, biotechnology, medical device, publishing houses, construction industries and academic institutions. We specialize in the strategic development, management and analysis of Clinical Research and Marketing & Business Development of our product basket, with fascilities fully geared to provide quality service to our valuable clients in right budget and committed to on time delivery.

Contact us :
Corporate Office :-
SYNCORP TECHNOLOGIES (P) Ltd
Novel Business Centre
No.10,100 Feet Ring Road,
BTM Layout 1st Stage.
BANGALORE – 560 068
INDIA
Tel : 9108032019521
Fax : 9108041201515

[Guest-IJT]

Ankita Yadav
-------------------------------------------------------
The submitted value of field named "Email :" is:
-------------------------------------------------------
anki.ankita11 AT yahoo.com
-------------------------------------------------------
The submitted value of field named "Designation / Name of the Post / Skill Set" is :
-------------------------------------------------------
Clinical research associate,Clinical research co-ordinater
-------------------------------------------------------
The submitted value of field named "Copy Paste Your CV / Resume Here :" is:
-------------------------------------------------------
RESUME
ANKITA YADAV
E-mail ID : anki.ankita11 AT ymail.com

CAREER OBJECTIVE
Seeking for the position in Clinical Research organization that will utilize my qualifications while offering several opportunities to integrate personal enrichment with professional goals.
AREA OF INTEREST
Clinical operations, Data management and Pharmacovigilance.
EDUCATIONAL QUALIFICATIONS
Currently : Perusing “Masters of CLINICAL RESEARCH” from “Institute of clinical research India” (ICRI).
2009-2010 : Diploma in Pharma business management, From ICRI.
March-2008 : Completed “B.sc Biotechnology” from “Devi Ahilya Vishwvidhylay” Indore, with 70% marks
March-2005 : Completed “Higher Secondary” from “M.P Board” with 74% marks.
March- 2003 : Completed “High School” from “M.P Board” with 70% marks.
SKILLS
- Able to work under optimal supervision
- Basic knowledge of SAS.
- Organization, planning and problem solving abilities.
- Negotiation skills.
- Established interpersonal and communication skills.
- Computer Knowledge.
POSTER PRESENTATIONS
Presented Poster on “International conference of harmonization” at Institute of clinical research India.
PROJECT
- Comparative study of ayurvedic & allopathic systems for the management of arthritis.
- Clinical Research in India (A SWOT Analysis).
SEMINAR ATTENDED
- Seminar on “TIME MANEGMEN’.
- Seminar on “FOCUS” at ICRI.
- Conference on Diabetics and cardiovascular disease in Dia care research in a’ bad.
SEMINAR GIVEN
As a part of curriculum activity seminar given on :
- Epilepsy Research
- Pharmacovigilance in India
- Prepared a protocol
- Prepared a patent application
- Application of ethics committee.
Nationality : Indian
Languages Known : English, & Hindi
Declaration :
I hereby declare that the above mentioned information is correct and I bear the responsibilities of correctness of the above mentioned particulars.
Yours Faithfully,
Ankita yadav
-------------------------------------------------------
More Information about this submission and submitter :-
___________________________________________________
Submission ID : 4110522
Date & Time : 9th May 2011 4:05 PM (UTC)
IP Address : 110.226.249.43
Browser Info : Mozilla/5.0 (Windows; U; Windows NT 6.0; en-US) AppleWebKit/534.16 (KHTML, like Gecko) Chrome/10.0.648.205 Safari/534.16
Predicted Country : Australia

[Guest]

Veeranna S S
E-mail : Veeranna.ss AT gmail.com
.................................................................................................... ..............................................
Career objective : Looking for challenging career in organization which would best utilize my skills and would provide me an opportunity to grow personally and acquire knowledge in my field by putting me on challenging assignments.
PROFESSIONAL EXPERIENCE :
1) Organisation : Infosys
Duration : 34 months (11-Jun-2007 to 1 April-2010)
Position : Senior Process Executive
2) Organisation : Lotus Labs
Duration : 6 months (Internship) from 18 June 2010 to 22 Dec 2010.
Position : Clinical Research Co-ordinator (Nasik, Maharashtra)
3) Hospital : Raga’s Skin care
DOJ : 1 April 2011 till the date.
Position : Clinical Research Co-ordinator
Project experience :
Protocol Title : A Multicenter, Double-Blind, Randomized, Vehicle-Controlled, Parallel-Group Study Comparing -------------------- In the Treatment of Mild to Severe Acne Vulgaris.
- Started the project from Site initiation level.
- Coordinating with Ethics committee regarding submission of Protocol, amended Protocol, SAE, deviation and other study related reports.
- Writing source documents (20 patients, 5 visits).
- Communicating with patients for their follow up.
- Hands on experience on E-CRF filling.
- Have good experience in handling E-CRF (updated 20 patients, 5 visits details)
- Providing Randomised IP’s to the patients.
- Maintaining logs and forms (IP log, Temp log, Randomisation log, patients visit tracking log, Screening log, enrolment log, etc)
- Updating and maintaining ISF and co-ordinating with CRA to update and maintain CSF.
- Experience of working under strict timeliness, meeting sponsor SLA.
Rewards :
- Got progression as senior process executive on 1 December 2008.
- Completed six sigma (Yellow belt) training on November 2008.
- Lead the first six sigma (Yellow belt) project and completed on September 2009 with soft savings of $1875USD.
- Got RAMP award for good performance.
- Received SPOT award for good performance and providing various process improvement ideas.
- Awarded with both Client and Infosys award for the best Team Player.
Additional Responsibilities :
- Reconciliation of daily activities.
- Working on daily and weekly client reports.
- Documentation of employees’ details in SAP.
- Handling Team meetings and organising Team building activities.
- Reviewing study Case Report Forms (CRFs) completed by the sites, and verifying entries by validating accurate source documentation to support CRF entries.
- Documenting site visits and issues in reports and follow-up letters to the site.
EDUCATIONAL CREDENTIALS
- A graduation in B.SC with Bio-technology, chemistry, and zoology has main subjects and has secured 84 % marks 2007 batch (Kuvempu university)
- PG-Diploma in Clinical Research from LCRA 2011 batch (LCRA).
(Knowledge on ICH-GCP, Indian GCP, Ethics committee, Regulatory bodies, ICMR guidelines, CDER, CBER, FDA guidelines, EU directives, 21 CFR part 11, part 50, part 54, 56, 312 and 314, SOP, Protocol, CRF, ICF, ISF, BA-BE studies, Clinical trial designs, Investigator meetings, EC submissions, site monitoring, clinical study reports, site close-out reports)
- Knowledge about Clinical Analytics 4.0