Clinical Research Associate CRA Ahmedabad, Delhi : Quintiles

[mskavi]

Quintiles Ahmedabad, Delhi/NCR : Clinical Research Associate

Website: http://www.quintiles.com/Careers/IndiaJobs.htm

Designation: Clinical Research Associate
Experience: 1 - 5 Years
Location: Ahmedabad, Delhi/NCR

Job Description:
The CRA conducts monitoring visits for assigned protocols and study sites. Overall responsibilities are to ensure that the study is being conducted in accordance with the protocol, standard operating procedures, good clinical practice, and applicable regulatory requirements.

- Performs site selection, initiation, monitoring and close out visits in accordance with contracted scope of work and good clinical practices.
- Provides monitoring visits and site management for a variety of protocols, sites and therapeutic areas.
- Completes appropriate therapeutic, protocol and clinical research training to perform job duties.
- Administers protocol and related study training to assigned sites and establishes regular lines of communication with sites to manage ongoing project expectations and issues.
- Evaluates the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalates quality issues to Clinical Team Lead and/or Line Manager
- Manages the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrolment, CRF completion and submission, and data query generation and resolution.
- Creates and maintains appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports and other required study documentation.
- May provide training and assistance to more junior clinical staff.

Desired Candidate Profile:
We are presently looking for candidates who have prior Clinical Monitoring experience in a CRO for atleast 1.5 years mandatorily.

Company Profile:
Quintiles Transnational helps improve healthcare worldwide by providing a broad range of professional services, information and partnering solutions to the pharmaceutical, biotechnology and healthcare industries.

Headquartered near Research Triangle Park, North Carolina, Quintiles has about 21,000 employees worldwide and offices in more than 57 countries.

Address:
Quintiles
3rd floor, Brigade South Parade
10,M.G.Road
Bangalore,Karnataka,INDIA 560001

Keywords: CRA, Clinical Research Associate

[Guest]

CURRICULUM VITAE
S. Nagaraju (2+ yrs of experience in CRO)
E-mail : nagaraju_sola AT yahoo.com; Mobile: 09963717149

Career Objective :
To be a member of a winning team, where innovation is meaning of life, motive is progress to learning and there is always way of doing things is the common belief.

Education Qualifications :
** Pursuing M.Sc (Clinical Research and Regulatory Affairs) Sikkam Manipal University 2007 to 2009
** B. Pharm Kakathiya University 68% (Ist Class) 2002 to 2006

Technical Qualification :
** MS Office Word, Excel, & Power Point

Professional Experience : (with one of the leading Contract Research Organizations)
Designation : Research Associate III
Organization : Contract Research Organization (Present employer kept confidentially)
Duration : Dec ’06 to present

Job Profile :
Carry end-to-end BA/BE studies which comprises of :
** Check protocol
** Get voluntaries in coordination with VMD Dept.
** ICF to voluntaries
** Finalization of voluntaries in coordination with duty doctors
** Check-ins
** Be in constant touch with voluntaries till study ends
** Ensure voluntaries comfort ness during the study
** Drug administration as per the protocol
** Collect samples in coordination with Phlebotomists
** Prepare report in E3 and E6 format and submit it to QA Dept.
** Send samples for BA Analysis
** Report presentations

Achievements :
** Individually accomplished 08 PIVOTAL STUDIES on various drugs related to Antihypertensives, CNS depressants, Ulcer, Antibiotics, Vitamins, etc..
** Successfully completed 05 PILOT STUDIES on various drugs related to Antihypertensives, CNS depressants, Ulcer, Antibiotics, Vitamins, etc

Additional Assignment :
** Ensure quality standards as per GCP guidelines
** Bios ample segregation
** Post-study activates
** Worked as a Q.C for 7 studies

Workshop participated :
** Workshop on Basics of Good Clinical Practices from the present organization
** Workshop on Bio-medical waste management ** handling & Safe disposal options from the present organization

Personal Profile :
Place : India (Andhra Pradesh), Hyderabad
Date of Birth : 10.02.1984
Age : 24yrs
Sex : Male
Marital Status : Single
Languages Known : English, Telugu, and Hindi

[Guest]

CURRICULUM VITAE
NAME : POOJA MANJHI (VERMA)
poojamjh4 AT gmail.com

CAREER OBJECTIVE :
Aim to be associated with a progressive organization & fast growing company with unlimited growth potential that gives me scope to update my knowledge and skills in accordance with latest trends and dynamically work towards the organization.
SUMMARY : I am Expert in following Products of SAS: -

SAS/BASES :
Creating Dataset From Different types of Raw Data (use of informant, formats, pointer controls and modifiers) Merging data sets (simple merging and using Proc Sql), Sub setting data using where, if, else if, if then do etc.
Functions :
Date Function, Character functions and numeric functions.

Different Procedures :
Proc Print, Proc Contents, Proc Sort, Proc Tabulate, Proc Report, Proc Transpose. Proc Printto, Proc Freq, proc append, Proc update.
Output Delivery System :
PDF, RTF and HTML, Customizing titles and Footnotes, customization of data using proc print (style) options.
SAS/STAT PROCEDURES : Proc Means, Proc Boxplot, ANOVA, Proc regression, Univariate, Proc Corr.
SAS GRAPHS : Proc Gchart, Proc Gplot, Proc gslide, Proc g3d, proc maps.

SAS/MACROS :
Macro processor flow, Macro components, Automatic macro variable, defining a Macro, Keyword Parameter and other ways of creating a Macros and using
PROC SQL :
Creating Table, Modifying Table, update Table, Functions and Different options in SQL, Joins, union through SQL.

HIGHLIGHTS OF EXPERIENCE :
** 2 years 5month of experience in marketing & Sales.
** Able to learn quickly, make effective decisions & problem solving skills with the ability to work with multi cultural environment.
** A proven track record of significant improvements in learning processes, productivity, quality, and customer satisfaction and maintaining a positive work environment.

PROFESSIONAL EXPERIENCE :
1.Organization – Johnson & Johnson (consumer division)
Designation- Professional marketing
Duration- (Dec 2008 – Nov 2009)
2. Organization- Chiron panacea Vaccines Pvt.Ltd.
Designation- ESMD (Executive- Sales marketing Development)
Duration- (Dec 2009- Present)

ACHIEVEMENTS & C0-CURRICULAR ACTIVITY :
** Contributed to achieve 2crors as a region in the month of sep-2010.
** Contributed to achieve annual target, we are in 100% Achievement as a region.
** Awarded as a best performer to sell highest flu vaccines all over the India.
** On occasion in world polio day conducted a camp in hospital and able to liquidate stock in large quantity as well as provided a proper information about vaccines and vaccination schedule to parents,

EDUCATION QUALIFICATION :
** B. Pharma-(63%) Rajiv Gandhi university Bangalore.(2005-2008)
** D. Pharma-(58%) Bangalore University.(2003-2005)

TECHNICAL SKILLS :
SAS BASE, MACROS, ODS, SAS/STAT SAS/access, SAS/Graph, SAS/Sql Analysis.

[Guest]

Amruta Rajaram Nalawade.
amruta.nalawade AT yahoo.in

KEY SKILLS : Knowledge of the clinical research and chemistry. Excellent organization, planning and problem solving abilities. Negotiation and time management skills.

OBJECTIVES :
To utilize my skills and abilities in impacting the success and growth of company as a leader in the clinical research industry. To obtain a Clinical Research Associate position in an environment where I will get a chance to utilize my knowledge. To study all industrial standards and establish all clinical trials ethically and perfectly.

ACADEMICS :
** Institute of Clinical Research (ICRI)
Pursuing Post Graduate Diploma in Advance Clinical Research (PGDACR)
In Mumbai campus at April –2011.
** University of Mumbai
Pursed Bachelor of Science degree in (Chemistry) degree, with first class
In Bhavan’s College at April 2010.
** Maharashtra State Board of Secondary and Higher Secondary Education, Pune.
Pursued HSC
In Bhavan’s College atFeb.-2007
** Maharashtra State Board of Secondary and Higher Secondary Education, Pune.
Pursued SSC,
In Dnynsagar vidyalaya at March-2005.
SPECILLISATION : Diploma in clinical research from ICRI (Andheri East)
Chemistry

PROJECTS/PRESENTATION :
Prepared presentation on- History of Clinical Research,
Lung Cancer,
Viral Disease,
Respiratory System.
Study Report :
Prepared study report on -
Vioxx

SEMINAR ATTENDED :
“Brand success : Highlights on safety aspects” on 27th November 2010, at Bharti vidyapeeth’s College of Pharmacy, Navi Mumbai.

OTHER QUALIFICATION :
I.T skill :
From Keerti Computer Institute done Keerti Professional course specialization in Windows-XP, Ms-Office 2003, Tally 9, D.T.P., Flash, HTML, DHTML, Java Script Dreamweaver, Fireworks, Gif Animator and Internet.

STRENTHS :
** Great team player.
** Managing time according to work

[Guest]

DEVEN BHAURAO BANSOD
Email- deven.bansod AT gmail.com

Professional Qualifications :
DBCR(Diploma in basic clinical research) from AECRT (Academy for ethical clinical research training) Nagpur in Dec2007.

Clinical Research Experience :
Total Experience in Clinical Research : 4 years
1) Working as Sr. CRC in Sushrut Hospital & Research Institute of Orthopaedics, Nagpur.
Duration : Sep 2009 to till date
2) Worked in Spectrum Clinical Research Pvt.Ltd, Mumbai.
Duration : 1 year from July 2008 to July 2009
Designation : Clinical Research Coordinator
3) Worked as CRC in Choudhary Hospital Kamptee, Nagpur.
Duration : 1 year from Jun 07 to Jun 08.

Involved in the following trials :
Sr. No Indication Phase Submission
1 Osteoarthritis III Domestic
2 Sleep Maintenance Insomnia III Global
3 Alzheimer’s disease III Global
4 Osteoporosis III Global
5 Osteoarthritis III Global
6 Rheumatoid Arthritis III Global
7 Adolescent Fibromylegia III Global
8 DVT III Global

Job Profile :
1 In-house monitoring of clinical trials at the site.
2 Review criteria for inclusion and exclusion
3 Maintenance of documents in the site file
4 Reporting of serious adverse events
5 Scheduling patient consultations and Follow-Up
6 Filling Up Case Report Form/eCRF’s
7 Coordination With Central Lab and Study Team
8 In house monitoring.
9 Maintenance of all Study related tracking log – Screening log, EC Submission log, Drug Accountability, Fax log, Couriering log, etc.
Current CTA : Rs. 2.2 laks per annum.

Educational Qualification :
Master of Science (Biochemistry) with 69% from Pandit ravishankar Shukla University, Raipur in 2006.
Skills :
** 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.
** Deep knowledge of monitoring procedures.
** Detailed knowledge of GCP and ICH guidelines including basic understanding o regulatory requirements.
Also Worked as ELISA and DNA analyzer in Innovative Genetics, Ahmadabad for 8 months from Oct 2006 to June 2007.

Conference and Meetings attained :
** Attained Investigator Meeting on DVT at Barcelona, Spain, Sep 2010
** Attained Investigator Meeting on Fibromylagia at Mumbai Aug 2010.
** Attained Clinical Trial Congress India 2010 at JW Marriott, Mumbai

Computer Knowledge :
Certificate course in M.S.Office, Knowledge of OCRDC, Inform systems. Also aware of IVRS and IWRS systems.

[Guest]

CURRICULUM VITAE
DR. SIMRAN CHHATWAL
simranchhatwal7211 AT gmail.com

CAREER OBJECTIVE :
** To gain practical knowledge and enhance and develop personal skills in a manner that helps in alleviating human sufferings.
** To gain exposure and enhance skills in Clinical Research

ACADEMIC SUMMARY :
M.D. in Pharmacology May 2009 – May 2012
Passed the Examination in the first attempt
Sri Guru Ram Das Institute of Medical Sciences and Research, Amritsar
Bachelor of Medicine Bachelor of Surgery(M.B.BS) June 1999 – March 2004
S S Medical College ,Rewa, MP
Passed the Examination in the first attempt
Completion of 1year internship 30th March 2005
S.S.Medical College,Rewa, MP
Permanent Registration no. MP 7211
Senior Secondary -XII (Science) March 1998(75%) Army Public School, New Delhi

PROFESSIONAL EXPERIENCE :
Worked as a resident (non-academic)at Indraprastha Apollo Hospital, New Delhi July- October 2008
Worked as a resident in Dept. of Ophthalmology at AIIMS, New Delhi July-September 2007

ADDITIONAL INFORMATION :
** Participated in the 30th National workshop on Clinical Pharmacology held at PGI, Chandigarh from 20th- 25th February 2012 and presented a scientific paper titled’ To Study the Antihyperglycaemic and Lipidlowering effect of Garlic as an adjunct to Metformin in patients of Type2 Diabetes Mellitus with obesity’.and was awarded the third position.
Attended the CME on ‘Modernizing Medical Training :Replacing Animals in MBBS Program’ held at Christian Medical College, Ludhiana on 20th January 2012
** Participated in the scientific programme on ‘PHARMACOVIGILANCE’ conducted by Knowledge Academy at Sri Guru Ram Das Institute of Medical Sciences and Research,Amritsar on 9th December 2011
** Participated in the ICMR-WHO-PGIMER Workshop on Clinical Trial Registry- India (CTRI) held at PGI, Chandigarh on 21st July 2011
** Attended the 43rd Annual Conference of Indian Pharmacological Society and International Conference on ‘Pharmacology and Translational Research’ held at National Institute of Nutrition, ICMR, Hyderabad from 13th-16th December 2010
** Attended the Conference cum Workshop on ‘PHARMACOVIGICON’ held at Lady Hardinge Medical College, New Delhi from 26th -28th November 2010
** Attended the CME on ‘ Alternatives to Animals In Medical Education’ held at Christian Medical College, Ludhiana on 27th February 2010
** Attended the 13th Annual Conference organized by the Punjab Ophthalmological Society held at SGRDIMSR, Amritsar from 18th-20th December 2009
** Was a part of the CME on Depression—An Update held at Christian Medical College, Ludhiana on 22nd September 2009
** Participated in the workshop on ‘ Clinical Research and Protocol Writing’ held at NIPER, Mohali from 24th- 28th August 2009
** Participated in the workshop on Cardiopulmonary Resuscitation and Airway Management-Oct 2003
** Part of the event management team for annual college festival -2002
** Participated in the 10th conference of MP State Chapter Indian Association of Preventive and Social Medicine-2001

INTERESTS :
Academic : Clinical Research
Non-academic : Reading(Fiction and Non-Fiction),water sports, music and travelling

I hereby declare that all the information provided by me in this application is factual and correct to the best of my knowledge and belief.

Date :
Signature :

[Guest]

CURRICULUM VITAE
ADITYA SHARMA
DOB : 13 DECEMBER 1987
E- MAIL : asharma1387 AT gmail.com

PROFESSIONAL DETAILS :
Registered with Indian Pharmacy Council

CAREER OBJECTIVE :
To be a part of good organisation, that encourages professional growth through wide range of challenging assignments, which would use my skills and knowledge to become a successful professional with reputation and recognised by the profession for expertise and knowledge.

PROFESSIONAL EXPERIENCE :
** Having experience of 2.5 years in clinical trials .
** Site selection , Site initiation ,site management and investigator undertaking, site monitoring visits.
** Presently working with RANBAXY Laboratories Ltd., Gurgaon (Haryana) as clinical research associate and handling Phase 4 and Phase 3 trials.
** Detailed knowledge of ICH** GCP including basic understanding of regulatory requirements.
** Earlier worked as a clinical research coordinator (Post Graduation Intern) at the Apollo Oncology Centre, Indraprastha Apollo Hospital, New Delhi handling phase 3 trialswith following job responsibilities.
** Coordinating site initiation visits.
** Submission of study protocols to ethics committee for approvals and all pre- study documentation requirements.
** Assist Principal Investigator in patient selection and clinical research study.
** Investigational Product accountability and dispensing.
** Scheduling patient visits and follow ups.
** CRF Completion.
** Assuring adequate reporting of adverse events.
** Prepare study status reports.
** Maintain study files on an ongoing basis to ensure that the files are complete and can be used as a source of reference.
** Ensuring that serious and non** serious adverse events have been recorded and reported in accordance with relevant SOPs.
** Manage the delivery of clinical study protocols, clinical study reports, study agreements, applications and other study documentation.
** Train internal and external study personnel in study specific procedures.
** Develop detailed study outlines and ensure medical and scientific input in study reports.
** Assist in non-project work and the development of clinical R&D procedures.

EDUCATIONAL QUALIFICATIONS :
2011 POST GRADUATE
CERTIFICAT COURSE
IN CLINICAL
RESEARCH INDRAPRASTHA APOLLO
HOSPITAL, DELHI 1st
2011 INTERNSHIP / TRAINNING
INDRAPRASTHA APOLLO
HOSPITAL, DELHI (Apollo Hospitals Research Foundation, New Delhi)
2010 B.Pharma.
Dr. K N Modi Institute of Pharmaceutical Education and Research, Modinagar , U.P. 1st
2003 Secondary CBSE 1st
2005 10+2 CBSE 1st

PROFESSIONAL QUALIFICATION :
** POST GRADUATE CERTIFICATE COURSE IN CLINICAL RESEARCH – completed recently from Apollo Hospitals Research Foundation , New Delhi
Modules Offered :
Module 1 : Drug Development
Module 2 : Pharmacokinetics & Therapeutic Drug Monitoring
Module 3 : Phases of Clinical Trials
Module 4 : Role of Ethics in Clinical Research
Module 5 : Basic Statistics and Research Methodology
Module 6 : Record keeping, Writing Reports and papers
Module 7 : Drug Regulation and Drug Laws in India and abroad
Module 8 : Laboratory Investigations
Module 9 : Clinical Trials Finance
Module 10 : Management of a Clinical Trial at a site
Module 11 : Clinical Trials Finance
Module 12 : Data Management in Clinical Trials
Module 13 : Clinical Trials in Children
Module 14 : Drug Reaction / Interaction / Information / Poisoning
Module 15 : Audits and Inspections
Module16 :Newer Approaches in Drug Research and Development

INTERNSHIP / TRAINING :
Internship / Training of one year from Indraprastha Apollo Hospital (AHERF), Delhi handled trials in areas :
1. Neurology
2. Oncology
3. Vector born diseases.
** One month vocational training in Psychotropic India Ltd., Faridabad (Haryana) (Production field).

EXTRA CURRICULAR ACTIVITIES :
** Active participation in Dr. K.N. Modi foundation sports Meet ZEAL 2007.
** Participated as shot put player at state level in year 2003

KEY STRENGTHS :
** Hard working and eye for detail
** Ability to work under dead lines and deliver
** Adaptability
** Excellent organisation, planning and problem solving abilities.
** Excellent interpersonal and communication skills.
** Knowledge on internet, Microsoft word, Microsoft Power Point.

PERSONAL DETAILS :
Gender : Male
Languages known : English, Hindi
Marital Status : Single
Father’s name : Sh. P. S. Sharma
Nationality : Indian

REFERENCES :
** Dr.R.K. Roy
Director
** Proff. V S Mathur ( pharmacologist)
Coordinator
** Dr Vibha Dhingra

I hereby declare that the information provided above are true to the best of my knowledge and belief.

ADITYA SHARMA

[Unregistered]

ANKITA GUPTA
Ankita Gupta,
E-mail- gupta.ankita83 AT gmail.com

OBJECTIVE :
To work in a challenging environment and contribute the best towards the progress of the organization, through my knowledge, innate skills and will to excel, to be in the organization that offers professional growth while being resourceful, innovative and flexible.

EDUCATIONAL QUALIFICATION :
** Pursuing Ph.D. from Government College of Ajmer.
** M. Phil.(Biotechnology) from M.D.S. University Ajmer with 77.00%
** M.Sc. (Biotechnology) from M.D.S. University, Ajmer with 67.25%
** B.Sc. from M.D.S. University, Ajmer with 70.02%
** Sr. Secondary (Science) from Rajasthan Board, Ajmer with 69.69%
** Secondary from Rajasthan Board, Ajmer with 77%

EXTRACURRICULAR ACHIEVEMENTS :
** ‘O’ Level & ‘A’ Level in Computers from DOEACC, Delhi.
** Won 3rd Prize in Quiz of Under Graduate Botany Association held at Govt. College, Ajmer in 2005
** Won 1st Prize in Debate Competition in 2002 held at Central Academy, Ajmer.

PROFESSIONAL EXPERIENCE :
** Eight Months Teaching Experience in M.D.S. University, Ajmer.
** Four Months Teaching Experience in Govt. Science College,Khokhra,Ahmedabad.
** Two years in Vikram A.Sarabhai Community Science Centre, Ahmedabad as Science Educator.

PROJECTS UNDERTAKEN :
** Ecophysiology of Some Selected Weed Flora with Special Reference to Interaction with Some Crop Plants of Ajmer District (Rajasthan).

Biochemical and Molecular Analysis of Kanji : An Ethnic Beverage of Rajasthan.

IN HOUSE SEMINARS :
** Nanobiotechnology
** Molecular Markers
** Tissue Culture
** Recombinant DNA Technology
** Cloning Vectors as Tools of Genetic Engineering

COMPUTER SKILLS :
** Proficient in Microsoft word, Excel, Power Point.

STRENGTH :
** Good Communication Skills
** Punctual & Time Management

PERSONAL DETAILS :
Marital status - Married
Date of birth – 03/08/1983
Father’s name – Mr Vinod Gupta
Languages known – Hindi and English

I hereby, declare that the information provided is best to my concern.

Place : Ahmedabad
Date : 22 /06 /2011

Yours Sincerely,
ANKITA GUPTA

[Unregistered]

JAGRUTI M. CHAVDA
Email ID : neha.five AT yahoo.co.in

CARRIER OBJECTIVE :
I am very eager to being my career in an industry which gives the right balance of both, exposure and value based knowledge that would finally make me a competent person in a chosen field. Also, it would be beneficial for the growth and advancement of the industry.

PERSONAL PROFILE :
Date of Birth : 5th June, 1988
Nationality : Indian
Marital Status : Unmarried
Languages Known : English, Hindi and Gujarati

ACADEMIC QUALIFICATIONS :
Examination Year of Passing Board/University CGPA*/Percentage
MPharm
(Q.A.) 2012 Charotar University of Science and Technology,
Ramanbhai Patel College of Pharmacy 7.31/10
B. Pharm 2009 Gujarat University, L. J Institute of Pharmacy 57.50 %
H. S. C. 2005 GSHSEB 63.33%
S. S. C. 2003 GSEB 84.86 %
*CGPA : Cumulative Grade per Annum

TECHNICAL SKILLS :
Handling of Analytical Instruments : HPLC, UVVIS Spectrophotometer, HPTLC
Computer knowledge : Basic, Internet surfing, Patent Search, Scientific Information retrieval, MS Office.

RESEARCH CAREER/ DISSERTATION :
My dissertation titles are
1. Simultaneous estimation of Telmisartan and Indapamide by U.V. Visible spectrophotometry in combination dosage form.
2. Development of Analytical Method for estimation of Ketoconazole in Pharmaceutical Dosagforms using High Performance Thin Layer Chromatography.
Guide : Mr. Manan Raval, Assistant Professor.
College : Department of Quality Assurance, Ramanbhai Patel College Of Pharmacy, Changa.

EXPERIENCE :
Worked as 1 month trainee at P&B pharmaceutical at Khambhat.

JOB EXPERIENCE :
Current Job at : Precise Formulation,
Prop.Precise Helth Care Pvt.Ltd.
Designation : Product Management Executive
Duration : Joining Date1st January 2013 to Till Date

SEMINARS/CONFERENCES ATTENDED :
Workshop on Intellectual Property Rights And Patent System (Sep2011) & (March2012).
Attended Workshop on Intellectual Property Rights with Special Emphasis on Biotechnololgy & Pharmacy2011, at P.D.Patel Institute of Applied Sciences, CHARUSAT, Changa (Anand) (March 2011).
Attended National Seminar on Recent Advances in Analytical Techniques For Pharmaceuticals2011, at Sardar Patel University, Vallabh Vidyanagar (March2011).
Attended refresher course of Pharmacy sponsored by state pharmacy council, at Ramanbhai Patel College of Pharmacy, CHARUSAT, Changa (Jan2011).
International Confference On Molecular Medicine (MOLMED Jan2011).
GUJCOST sponsered One Day National Seminar On “Application OF STATISTICAL ANALYSIS AND COMPUTER GRAPHICS IN PHARMACEUTICAL RESEARCH”(Sep.2011).
Attened workshop on DRUG REGULATORY AFFAIRS held at Ramanbhai patel college of Pharmacy (April2012).

HONORS & AWARDS :
Qualified GPAT 2010, condudcted under the aegis of AICTE, New Delhi, Organized by The M.S. University of Baroda.
Have published Paper in AJRC (Asian Journal Of Resaerch in Chemistry) of Tital Simultaneous estimation of Telmisartan and Indapamide by U.V. Visible spectrophotometry in combination dosage form.
Participate in poster presentation entitled “Modern analytical techniques use in herbal drug with special reference to High Performance Thin Layer Chromatography” in “PHARMAESCAPADE 2011”, organized by Sigma institute of Pharmacy, at Bakrol, Vadodara.(Oct 2011)

AREA OF INTEREST :
Quality AssuranceQuality Control
Regulatory Affairs,
Product Management Team

STRENGTH :
Communication Skill, Presentation Skill,Positive Attitude, Selfconfidence & Enthusiastic to learn new things.

DECLARATION :
I, Jagruti M Chavda , hereby affirm that all the details furnished above are true and correct to the best of my knowledge and belief.

Date :
Place :
Name : Jagruti M. Chavda

[Unregistered]

CURRICULUM VITAE
Venkatarao Vankadari
Email Id : venkatmmth267 AT gmail.com

Objective :
To achieve a responsible and challenging position as research and development, work individual Strength, creative, and experience is utilized to endorse the organization in the best possible way.

FIELD OF INTEREST :
Clinical Research Associate
C.R KNOWLEDGE
Drug Discovery & Devolopment
Ethics in Clinical Research
Regulatory Guidelines
Audits & Inspections
Clinical Trial Management
Clinical Data Management
Pharmacovigilance
Medical Writing & Bio Statistics

EDUCATION QUALIFICATIONS :
DEGREE INSTITUTE BOARD/UNIVERSITY YEAR OF PASSING OBT MARKS% :
P.G.Diploma in clinical research Focus institute of clinical research Focus edu care 2012 50.33
B.Sc (Biotech) S.S.N.Degree college Acharya nagarjuna university 2010 60.00
Intermediate Jawar Bharathi jr college Board of intermediate 2006 52.00
S.S.C A.P.R.School Board secondary education 2003 73.66

COMPUTER KNOWLEDGE :
Operating systems : Windows95/98/2000/XP, VISTA, Windows7.
Language known : Oracle clinica, SQL Server2008, MS Office.
PERSONAL STRENGTH AND ABILITIES
Hard working is one of my primary assets,
Positive Outlook, Quick Lerner

HOBBIES :
Writing short stories in Telugu,
Making new friends,
Surfing Internet.

ACHIEVEMENTS :
Awarded first prize in technical quiz competition the occasion of college
Day celebrations.
Awarded Best student in my school days.

PERSONAL PROFILE :
Father’s name : Mr. Ramulu
Date of birth : 10071986
Gender : Male
Marital status : Married
Nationality : Indian
Languages known : Telugu, English and Hindi.

DECLARATION :
I hereby assure that information I furnished above is true to the best Knowledge and belief.

Place :
Date :
VENKATARAO.V