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[QUOTE=Guest-IJT;102191]Dear Sir
I Nishant Kharb have done MSc in Clinical Research in year 2008. Earlier i have done my graduation in Pharmacy.

Working Experience- Working as CRA (Clinical Research Associate)
Venus Remedies Limited Panchkula (Chandigarh)
Total Exp-1.10 year
Current CTC- Rs 2.4lac/annum

Looking to work as CRA in estmeed organization
Kindly find my CV as word attached document
Thanks & Regards
Nishant Kharb
Contact No- +919318596407(Mb)
+919780503598(Mb)

Curriculum Vitae

NISHANT KHARB
H.NO-2091 GULABI BAGH
DELHI-110007
Email-nishantkharb AT gmail.com
Contact No+919318596407(Mobile)
+919780503598(Mobile)
011-23655059(Home)
________________________________________

- Career Objective
Looking a position that offers me an opportunity for advancement in my career endeavors, where I can utilize my current technical skills, knowledge & can complete my project from conception to completion under a boss who can take best out of me & gives me a chance for my innovative work as well.

- Presently Working

Venus Clinical Research Services (VCRS) is a
Clinical Research Organization (CRO)
Plot No-51 -52 Phase -1 Industrial Area
Panchkula Haryana (India)

Website:[url]www.venusmedicineresearchcentre.com/vcrs[/url]

Designation- CRA (Clinical Research Associate)
21st March 2008 to till Date

VCRS is a Clinical Research Organization (CRO) services provider to pharmaceutical and biotechnology companies. VCRS offers clinical trial project management monitoring, auditing, medical writing, and regulatory services and is involved in cost-effective (Phase I, II, III and IV) clinical trial studies. VCRS is also involved in doing preclinical studies.

VCRS is a subdivision of Venus Medicine Research Centre (Venus Remedies Limited). The VRL(Venus Remedies Limited) is a leading Pharmaceutical company in India which is mainly manufacturing Antibiotics, Cephalosporin’s and anticancer agents. It has been accredited by E.U GMP,W.H.O G.M.P. Uganda GMP and Zimbabwe GMP certificate etc. Recently Venus was felicitated by ICICI Bank, CRISIL and CNBC TV-18's "Emerging India Awards"most recently for its exemplary growth.

ICATION
- Job Profile

- Doing clinical site feasibilities studies & clinical site identification starting from phase-1 to phase –IV studies
- Doing monitoring of Clinical trial site to know whether principal investigator/investigators are doing the clinical study as per the protocol, ICH- GCP, SOPs
- Assisting in preparation of I.B (Investigators Brochure), Protocol, paper CRF & informed consent form, SOPs etc
- To assist in the preparation of SOPs and ensuring their implementation
- Maintenance of all essential documents before the clinical study, during the clinical study and after completing the clinical study
- Doing site close out visit.

Academic Profile
Year of passing Degree University

2006-2008 MSc –Clinical Research
Cranfield University U.K.

2007 PGDPM (Post Graduate Diploma in Pharmaceutical Management) ICRI
2006 B. Pharmacy Maharshi Dayanand University Rohtak

Schooling

Year of passing Qualification Board

2001 Intermediate {12} CBSE

1999 High School {10} CBSE

- Computer Skill
MS Office, Window 2000/XP,
Linux
- Publication/Conference Attended
- Manu Chaudhary, Nishant Kharb, Dr. Rajesh Sehgal . Comparative Efficacy and Safety evaluation of FDC of Ceftriaxone_Sulbactam with modified solvent for reconstitution V/s water for reconstitution in patients with bacterial infections.(Accepted)
- Manu Chaudhary, Nishant Kharb, Dr. Rajesh Sehgal. An open labeled, Post marketing surveillance study to evaluate the efficacy and Safety of Fixed dose combination of Ceftriaxone –Sulbactam in neonatal and pediatric patients suffering from various bacterial infections (communicated)
- Manu Chaudhary, Nishant Kharb, Dr. Rajesh Sehgal. An open labeled, 3- arm comparative study to evaluate the efficacy and Safety of combination of Ofloxacin-Ornidazole Vs Ofloxacin and Metronidazole in patients suffering from various bacterial infections (communicated)
- Attended 9th Annual Conference on Pharmacovigilance in India organized by Society of Pharmacovigilance India (SOPI) held at Sirsa (Haryana) in Nov 2009
- Attended Conference on Clinical Research which was held at NIPER, S.A.S Nagar, Mohali (Punjab) in Feb 2009
- Attended 7th Annual Conference on Pharmacovigilance in India organized by Society of Pharmacovigilance India (SOPI) held at Jaipur (Rajasthan) in Nov 2007

Achievements
- Initiated 14 Clinical Trial Sites
- Prepared 4 Protocols for various phases of clinical trials & 4 Investigator Brochures for the same.
- Completed one PMS study & initiated two phase-3 multicentric studies & one phase-1 clinical study as well
- Written clinical study report for PMS

Personal Details
- Date of Birth : 22nd August 1984
- Marital Status : Single
- Gender : Male
- Languages Known : English, Hindi.
- Nationality : Indian

- Declaration
I hereby declare that above information is true to the best of my knowledge & nothing has been concealed herein.
Date:
Place:
NISHANT KHARB[/QUOTE]

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