B Pharmacy Resume Format for Freshers in Doc and PDf

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Anjali Kumari

DNO 15-12-13, RAM SHARMA STREET, HANUMANPET, VIJAYAWADA, PIN: 520124.

                  Ph.: (M) +91 9546258642 E-mail: anjali65214@gmail.com

 

   To explore the software industry and learn as much as I can, in the process would like to pursue a    carrier in the industry and grow along with the organization I work for.

 

 

Summary

 

·         Extensive knowledge on SAS/BASE, SAS/STAT, SAS/MACROS, SAS/SQL, SAS/ODS.

 

·         Extensive knowledge on REPORT generating procedures like PROC FREQ, PROC MEANS, PROC UNIVARIATE, PROC TRANSPOSE, PROC FORMAT, PROC REPORT  etc.

 

·         Knowledge on Generating Tables, Listings  as per company standards and in compliance with 21 CFR Part 11, FDA and other regulatory compliance.

 

·         Knowledge ON CDISC SDTM.

 

·         Knowledge on analysing the data, generating reports, tables, listings and graphs.

 

·         Knowledge on Phase-II & Phase-III Clinical Trials, performed clinical data analysis and generated SAS datasets in accordance with the SOPs and guidelines.

 

·         Exposure to clinical trial data such as demographic data, Adverse Events(AE), CM data, Laboratory data (Lab data)  and Vital Signs.

 

·         Knowledge in Generating Output files in RTF and PDF using SAS/ODSs.

 

·         Ability to work on multiple tasks and strong interpersonal, analytical and presentation skills.

·         Excellent in analytical, presentation, communication and work independently as well as in a team.

 

·         Educational Background in Clinical and pharmaceutical field with very good knowledge of Biostatistics.

SDTM

·         Knowledge about classifying  general observation class,special purpose domains etc.

·        Good understanding of CDISC SDTM models and  in converting legacy data to CDISC SDTM (Study Data Tabulation Model) Standards.

·         Having knowledge in Creating SDTM datasets as per CDISC SDTM Standards (3.1.2).

·         Performed CDISC mapping for current trials and classified data into domains such as                 Demographics (DM), Concomitant Medication(CM),Medical History (MH), Adverse Events (AE) ,Vital Signs(VS) ,Laboratory Tests Results(LB)..

·         Basic Knowledge  in Understanding CDISC Domain Specifications

·         Knowledge in validating CDISC SDTM Domains by using cdisc validator.

·         Basic knowledge  in understanding of Study Protocols, SAP (Statistical analysis plan), and CRF’s.

·         Knowledge in Creating SDTM datasets for safety and efficacy domains 

 

 

TECHNICAL PROFICIENCIES:

SAS Tools:                      V9.2, SAS /MACROS, SAS/SQL, SAS/STAT, SAS/ODS.

SAS Procedures:             Report, Print, Freq, Means, Summary, Univariate, Sql, Sort, Transpose

                                           Contents, Options, Import, Export, Format, GPLOT.

Operating System:          Windows,linux.

Office tools:                   MS-OFFICE,MS-ACCESS,MS-WORD,MS-EXCEL.

 

 

Strengths:

·     Ability to deal with people diplomatically

·     Highly motivated with a keen understanding of the latest technologies and an inherent passion for Learning.

·     Self-motivated and Self-managing. Results oriented.

·     Positive attitude and enthusiastic in teamwork.

·     Ability to handle crunch situations and adapt to any environment.

·     Quick adaptation to new ideas and methodology.

Academia:

·     b. Pharmacy from Nirmala College of Pharmacy affiliated to Acharya Nagarjuna University, Guntur  in 2013 with 72%.

·     IPE from Narayana Junior College, Vijayawada in 2009 with 88%.

·     SSC from Sri Kakatiya high school, Vijayawada in 2007 with 83.2%.

 

Extra curriculum activities:

·         A postal presentation given in IPA CONVENTION 2012  in manipal university. and also participated in various institutions.

·         Attented national seminar conferences.

·         Have participated in various Cultural activities and achieved awards.

·         Have participated in various Quiz competitions.

·         Participated in blood donations camps conducted by Red cross society.

·         Participated in NSS Camps conducted by our institution.

 

Key intreast:

·         To make carrier as a clinical sas programmer

          

 

Project done in my institute:

Therapeutic area: cardiology

Description:

A Double-Blind, Randomized, Placebo-Controlled ,multicentral, paralel assignment  Trial to  Evaluating The Safety And Efficacy Of the study drug . 

Responsibilities:

 

• Responsible for creating tables and listings as per the sap
• Analyzing the clinical trail data with the use of various sas products
• Responsible for report validation .
• Extensive usages of procedures like means,freq,contents,sort,transpose format,compare.
• Extensive use of function for clear the cosmetic errors
• Creating macros and usage of standard macros to optimize the code.
• Creating user define formats by using proc format
• Create the reports with the use o proc report and tabulate
• Exporting the analyzed data to client based on requirement with use of ods statement

 

Personal Dossier:

 

Linguistic Proficiency     :               English & Telugu

Location Preference       :               Anywhere in INDIA                           

                                                                                                                                                              

                 (Anjali kumari)

  

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