www.icbio.org Clinical Research Pvt Ltd Delhi : Clinical Research Associate

[mariammal]

Name of the company : ICBio Clinical Research Pvt Ltd
Location of the company : DELHI
Designation : Clinical Research Associate

Job Specification :
Job Opeinig : Clinical Research (Associate Academic Incharge)
No. Openings : 20 +
Salary (RS/PA) : 1,50,000 to 6,00,000 + Yearly Bonus + Performance Incentive + Education Facility
Qualification : Medical Professionals ( Post Graduate / Gradudate i.e M.Sc, M.Pharacy,M.B.B.S,BDS,B.TEC(Bio),M.Pharmacy / B.Pharmacy)
Job Location : DELHI NCR - Rewari Center
Experience : 3 years (Freshers can also apply)

Corporate Trainer (M/F): Qualification: Post graduates in life Science any one of the following clinical Research, Biochemistry, Biotechnology, Microbiology or M.B.B.S/B.D.S/ B.Pharma/ M.Pharma with exposure to Clinical research / clinical Data Management.
Candidate should be Smart, Aggressive, and Energetic, Self Stator with good communication skills.
Pleasing personality and flair knowledge of Clinical Research / Clinical Data management.
Fresher can also apply for the posts.
You can also work as visiting faculty, if you are working in Clinical Research / Clinical Data management companies.
Send resume, cover letter, references to:
Email id: career@icbio.org

Business Development executive:
Qualification: MBA or Post graduates in life Science any one of the following Biochemistry, Biotechnology, and Microbiology with exposure to Clinical research and Clinical Data Management.
Candidate should be Smart, Aggressive, and Energetic, Self Stators with good communication skills.
Pleasing personality and flair knowledge of Clinical research/ clinical Data Management.
Good English writing Skills.
Good research skills on internet
Send resume with cover letter to:
Email id: career@icbio.org

Website : http://icbio.org/index.html

How to Apply : Kindly send your updated CV to Dr Shalu Vashistha (Academic Head) drshalu@icbio.org, info.rewari@icbio.org

Address of the company :
ICBio Clinical Research Pvt Ltd
Rao Bhawan, Gopal Dev Chowk,
Rewari , Haryana - 123401,

About the company :
Innovative Centre for Biosciences (ICBio) was established in the year 2005 under the aegis of the Mahatma Gandhi Education Trust (MGET), a Non- Government Organization (NGO) of likeminded, elite professionals and academicians from various segments of the society.

General Instructions :
1) This is a job / career / vacancy / recruitment posting from ICBio Clinical Research Pvt Ltd at DELHI for post of Clinical Research Associate .
2) For more details refer company website of ICBio Clinical Research Pvt Ltd .
3) You can send your resume / CV to the careers e-mail id of the company (ICBio Clinical Research Pvt Ltd ).
4) Source of this info is the company website / internet on the date of publishing.

[vankashri@gmail.com]

PUSHPA LATHA.VANKA
E-Mail :-vankashri AT gmail.com
CAREER OBJECTIVE
- Seeking for the position of Clinical Research in the medical field while merging into a globally focused organization that will purposefully utilize my qualifications while offering several opportunities to integrate personal enrichment with professional goals.

ACADEMIC QUALIFICATION
Course Board/University Year of passing Percentage
Master in Pharmacy-
Pharmacology SASTRA University, T.N 2011 74%
Bachelor in Pharmacy Acharya Nagarjuna University ,A.P 2009 74%
Intermediate Bi.P.C Board of Intermediate, A.P 2005 83.5%
S.S.C Board of Secondary Education, A.P 2003 82%
SPECIALIZED SKILLS
- Deep knowledge of monitoring procedures.
- Detailed knowledge of GCP and ICH guidelines including basic understanding o regulatory requirements.
- Comprehensive knowledge of Covance S.O.P.'s for site monitoring.
- Basic knowledge of clinical trial process.
PROJECT WORK
- Bachelor in Pharmacy :-
In pharmaceutical analysis – NEW SPECTROPHOTOMETRIC METHODS FOR THE DETERMINATIONS OF AZTREONAM.
- Master in Pharmacy-Pharmacology :-
In Preclinical studies--SAFETY ASSESSMENT OF NATURAL PRODUCT LI 12508 ON RATS in TOXICITY DEPARTMENT - LIALA IMPEX R & D CENTER in A.P.

STRENGTHS
- Able to work under optimal supervision
- Excellent organization, planning and problem solving abilities.
- Excellent negotiation and analytical skills.
- Established interpersonal and communication skills.
- Fluent in English and other local office languages both verbal and written.
- Proficiency in computer.
- Able to work effectively and efficiently in a matrix environment.
WORK EXPERIENCE & TRAINING
TRAINING :-

- Participated in workshop/Training program in the “BASICS OF CLINICAL RESEARCH & ICH-GCP” at Vissannapeta, A.P
INTEREST AREA :
- Pharmacovigilance (PV) and clinical operations
SKILLS :-
- Computer : - M.S office, SPSS, FoxPro
- Languages : - Telugu, English, Hindi ,Tamil
CERTIFICATIONS
- Participated in the 60th ” INDIAN PHARMACEUTICAL CONGRESS “ held at NEW DELHI-DEC 2008.
- Poster presentation PHARMA QUEST ‘2Kg’ on ” DRUG INTERACTION” which was held Feb 2009 at DR.SAMUEL GEORGE INSTITUTE OF PHARMACEUTICAL SCIENCES- Markapur A.P
- Participated in one day workshop/Training program in the “BASICS OF CLINICAL RESEARCH & ICH-GCP” at Vissannapeta, A.P

[Guest]

HASAN MALIK

E-Mail : hasanmalik.cr AT gmail.com
________________________________________

Career Objective :
Looking for an opportunity to synergize my abilities, skills and efforts in tandem with the demanding performance standards of the company and helping in achieving its goals and objectives.
________________________________________
QUALIFICATION
- ACADEMIC QUALIFICATION-
Graduate with a Hons degree from Delhi University.
SSC Passed from HBSE with first division.
- PROFESSIONAL QUALIFICATION-
PGDCR (Post Graduate Diploma in Clinical Research)regular, from Sharda University.
(Pursuing)

- TECHNICAL QUALIFICATION-
Done computer Courses from NIIT & Indian Institute of Education
________________________________________
EXPERIENCE

- DESIGNATION : Team Leader
COMPANY : Corporate Infocom Pvt. Ltd
DURATION : January, 2009 to July, 2009
- PROFILE : Observer
DEPARTMENT : Department of Cardio-Respiratory Physiology. VBPCI
DURATION : 26, May 2009 to 27, June 2009
ACADEMIC CREDENTIALS
DEGREE COLLEGE/SCHOOL UNIVERSITY/BOARD YEAR OF PASSING
PGDCR(regular)
(clinical research) School of allied health and science
(Sharda university.G.Noida
2010-11
GRADUATION
SGTB khalsa college ,Delhi university
Graduate with a Hons degree from Delhi University.
University of Delhi 2010
12TH
JP.Jain Sr. Sec. School, Sonipat.
Board of School Education Haryana 200
PROJECT/WORKSHOP/SEMINARS
Attended National Workshop on Clinical Research (Sharda University in Collaboration with ICMR.
Project and summer training at VB Patel Chest Institute & Research Centre in PFT Deptt.

Actively participated in National Symposium on Forensic Sciences at Delhi University.

Attended Seminar on Renewable Energy by Dr. P.C. Pant, Director in Ministry of New and Renewable Energy.
Delivered various Seminars at College Level.
________________________________________
Achievements :
- Member of student union of India.
- Treasurer of department for one year at Delhi university
- Member of departmental society in college.
- Member of cricket team
- Participated in university level seminars
- Participated in many management activities at college level
- Organized various events.
________________________________________
KEY SKILLS
Behavioural Skills :
- Good Communication skills with Strong Interpersonal skills.
- Stress management, Building self esteem.
- Aptitude for updating knowledge
Managerial Skills :
- Enjoy new challenges and willing to take initiative and extra responsibilities to get
work done.
- Team Player.
- Possess Leadership Qualities.
Strengths :
- Assertive.
- Punctual.
- Optimistic
- Adaptive

[Guest]

Hi sir/Maam
Am venkatesh studying Mpharamcy III sem in Vaageswari college of Pharmacy (KU), I want to do my project work in your company with any one thefollowing topics :Preparation and characterization of
Microsphers
Liposomes
Nano particles
Buccal patches
Am good at practical knowledge and instruments in laboratory. So kindly accept my reqest.
Resume
Name : Venkatesh.K
Mail Id : venkateshkokkula1 AT gmail.com

____________________________________________________
Objective : To prove myself by delivering my level best at the task given by you and
partnering in achieving new heights.
Educational Qualifications :
Course College Year University % of Marks
M.Pharmacy Vaageswari College of Pharmacy, Karimanagar 2010-12 Kakatiya Pursuing
M.B.A Pragati Maha Vidyalaya, Hyd 2010-13
IGNOU Pursuing
B.Pharmacy J.J college of Pharmacy, Maheshwaram, RR 2006-10 JNTU 68.97
Intermediate APRJC, Nimmakuru, Krishna 2003-05 BIE 93.2
SSC ZPHS Awadam, Adilabad 2002-03 - 85

[Guest]

CURRICULUM VITAE
UMA HUMBI
Email : uma_humbi AT yahoo.com
CAREER OBJECTIVE :
Opportunity to make worthwhile contribution to organization utilizing the knowledge gained so far and continuously upgrading the same for the development of the organization and self-improvement.
EXPERIENCE :
Presently associated with Genovo Development Services Ltd. (Medreich group company), Bangalore, in Formulation Development as Officer - Reseach and Development since August 2009 to till date.
JOB PROFILE :
- Product development for Europe and Indian markets.
- Carrying out search for scientific and technological literature including patents and regulatory updates.
- Performing perfomulation studies of API in relation to excipients.
- Establishing stability protocols for drug-excipient compatibility studies.
- Characterization of Reference listed drug product and preparation of data sheet covering physiochemical and performance characteristics.
- Designing proto-type formulation for Tablet dosage forms.
- Conducting and optimizing various coating operations and composition of tablets.
- Addressing the trouble shooting during various development activities.
- Designing and monitoring stability protocols as per ICH guidelines for drug product.
- Stability data analysis and data interpretation.
- Recording all the experimental results and observations in laboratory note books as per cGMP requirements.
- Preparation of Master formula Records, Batch manufacturing records, Product validation protocols, Hold time study protocols, Technology transfer and process validation, In – process product specifications.
- Preparation of SOPs.
PROJECTS HANDLED :
- Development of bioequivalent solid oral dosage form (Extended release tablets) for Indian market.
- Development of bioequivalent tablet dosage forms for Europe market.
TECHNICAL PURVIEW :
- Compression Machine
- Rapid Mixer Granulator
- Fluidized bed dryer
- GPCG 1.1
- Coating Machine
- Dissolution Tester
- UV Spectrophotometer
ACHIEVEMENT/ACADEMICS :
- Qualified Graduate Aptitude Test in Engineering “GATE” during the year 2007, secured 1206 all India rank.
Sr.
No Qualification Institute/university Year of passing Percentage
1. M. Pharm Nitte Institute of Pharmaceutical Sciences, Mangalore, Rajiv Gandhi University of Health Science, Bangalore, Karnataka.
2009 80.00
2. B. Pharm Nitte Institute of Pharmaceutical Sciences, Mangalore, Rajiv Gandhi University of Health Science, Bangalore, Karnataka.
2006 73.42
M. PHARM RESEARCH PROJECT :
Title : “Ion- exchange resin based taste masked orodispersible formulations (Tablets and Films) of bitter drug Levocetirizine Hydrochloride”. Ion exchange resins used are Indion 204, Indion 234, Tulsion 335, Tulsion 339.

COMPUTER PROFICIENCY :
- Higher Diploma in Computer Science

[shaileshpatil]

Shailesh Kashinath Patil
E-mail – shailesh.mhrc AT gmail.com

¬¬¬¬¬¬¬¬¬¬¬¬¬¬¬
Power Statement
To obtain a position that will utilize my talent and potential to meet the goals of the organization and provide me personal and professional growth in clinical research.
Experience
Name of organization : Mehta Hospital and Clinical Research Centre, Ahmedabad
Duration : Oct 2009 – Till Date
Designation : Clinical Research Coordinator
Responsibilities : Perform Service at the Investigator Site in accordance with ICH GCP guidelines,
Applicable Local Regulatory and EC requirements and the approved study Protocol.
- Prepare & Review document For EC communications.
- Prepares for and assist at the Site Initiation Visit, Interim monitoring Visit and the Close out visit.
- Maintenance of ISF and other trial related study documents.
- Completion of CRFs/eCRF, From the Source Documents with ensuring accuracy of all records.
- Review completion of all protocol related procedure /assessments by the responsible Investigator, which would include scheduling, Subject screening and Enrolments.
- Assist timely resolution of Data Clarification Forms/ Data Queries.
- Maintain Study Inventory of all the Clinical trial supplies including, Lab Kits and Study Medication and Study Documents.
- Documenting an Adverse Event and Reporting to Sponsor, IRB/IEC.
- Perform any other study related co-ordination function as required by specific protocol or assigned by the Investigator.
- Ensure that the Investigational Product (IP)’s are stored at required temp and maintain the IP Accountability log.
Project Summary
Sr. No. Indication of Trial Clinical Phase of Trial Role in Trial Year in Which Trial Was Conducted
1. Idiopathic Pulmonary Fibrosis III Study Coordinator Dec 2011 to ongoing
2. Acute Bacterial Skin & Skin Structure Infection III Study Coordinator Dec 2011 to Ongoing
3. Invasive Fungal Infection IV Study Coordinator March 2011 to ongoing
4. DM type-2 III Study Coordinator Jun 2010 to Nov 2011
5. Asthma IV Study Coordinator Jan 2010 to Dec 2010
6. DVT (Deep Venous thrombosis) III Study Coordinator Oct 2009 to Aug 2011
7. AF (Arterial Fibrillation) III Study Coordinator Oct 2009 to Dec 2010
Area of Interest
- Clinical Research Associate
- Clinical Trial Assistant
Academic Credentials
2009 PG Diploma in Clinical Research Affiliated by ACRP, from Bilcare Research Academy, Pune, (MH).
2008 B.Sc. in (Microbiology), from North Maharashtra University, Jalgaon, Maharashtra.
2005 Diploma in Medical Laboratory & Technology from MTRI, Pune, Maharashtra.
Computer Skills

Microsoft Operating System, Internet – Proficient.
Certificate Program
- Successfully completed the NIH Web-based training course “Protecting Human Research Participants”. On 26/Mar/2010
- Successfully completed Quintile GCP Module (1 to 6) of Certificate of Completion on 15-Jul-2010.
- Successfully completed CAPA (Corrective And Preventive Action) on 01/Aug/2010
- Completion of PPD Electronic Data Capture Training OC RDC (Site)-(4.5.3.) on 04 July 2010 and 16 Sep 2011
- Completion of ICH GCP web based training of Royal Holloway University of London. On Aug 2010
- Successfully Completed RDC onsite Web Based Training (BI) on 17 March 2011.
Workshop Attended

- Attended workshop on clinical drug trial with special reference to RA/OA knee on 14th Nov. 2008 organized by Indian Rheumatology Academy at Pune.
- Attended ICH-GCP training and Clinical Research Site Coordinator course From “Safe Search Independent Ethics Committee” (SSIEC) From Ahmedabad on 01/Dec/2009.