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my past experiences and skills focused on Biochemistry, molecular biology, Signal Transduction and Cancer biology involved in Medicine usages and its Applications. i have experience in various biochemical techniques e.g. Cell Culture, western blots, reporter Gene Assays etc. i also have experience on DNA-RNA work, co-Immunoprecipitation, Western blot ,Cell Culture ,ELISA and have theoretical background on facs, Immunofluorescence, fret,frap ,immunological methods and Microarray processes. i am a sincere and hard working person. this is reflected from my good academic record. i qualified net (national eligibility test), which is the entrance exam to pursue phd studies in india with all indiarank of 48. i have also done a specialized course in the field of Clinical trials which gave me an exposure to the following: terminology and common trial designs Randomization – what is it and how do we do it blinding Treatment – why and how we keep everyone in the dark about the Treatment selecting outcome – good and bad ones analyzing the data – principle of intention-to-treat, why it’s not crazy reporting the results – consort guidelines, a good road map for readers and writers ethical issues – why they are important and what they are currently i am looking for a job/internship as a biochemist


Current Experience

  • Technical Support in Clinical Trials & TMF archiving

    Since April 2015

    preparation for submission packages for submissions to the authorities for Clinical trials. preparations for submission of amendments, dsurs and keeping a track of the submissions.also uploading the packages in tmf, qc checks and updating the duties include:


    • track, distribute and file documents as they are returned
    • maintain the electronic/paper trial master file (tmf)
    • prepare and send study materials to Investigator sites
    • attend study meetings and arrange Investigator meeting Logistics
    • prepare essential Clinical Trial documents
    • archive documents

    Preparation for submission packages for submissions to the Authorities for Clinical Trials. Preparations for submission of Amendments, DSURs and keeping a track of the submissions.Also uploading the packages in TMF, QC checks and updating the trackers.My duties include:


    • Track, distribute and file documents as they are returned
    • Maintain the electronic/paper Trial Master File (TMF)
    • Prepare and send study materials to investigator sites
    • Attend study meetings and arrange investigator meeting logistics
    • Prepare essential clinical trial documents
    • Archive documents

  • Pharmacovigilance & Clinical Data Management

    Since August 2014

Past Experience

  • Data Management Specialist EVMPD

    October 2014 --- March 2015

  • Research Assistant

    April 2013 --- November 2013
    my project dealt with a post translational modification Enzyme, artd10, which is the 1st discovered monoadp ribosylating Enzyme and has diverse effects in cell proliferation, differentiation, cell cycle and even cell death. during this project i got an experience of various techniques like Cell Culture, western blots, reporter Gene Assays, cloning, and transformation and plasmid isolation.

  • Project Intern

    January 2012 --- March 2012
    the project“dependence of poor people on ganga, in varanasi, as the only source of water and its consequences”. the topic was related to epidemic study of water borne Infectious diseases and gave an insight of Epidemiology studies.

  • Project Intern

    May 2010 --- July 2010
    the project i was involved in, was related to expression and Purification of a membrane Protein. a bacterial outer membrane Protein was expressed and purified using various Purification steps (urea lysis method, affinity Chromatography, dialysis, Western Blotting, and bradford method for estimation of Protein).this Protein was fused with lipid to form liposomes which will be developed into Vaccines against the Pathogenesis of the Bacteria.


LinkedIn Assessment :
Biochemistrymolecular biologyWestern BlottingPCRCell CultureOperations ManagementMicrobiologyClinical trialsImmunofluorescenceImmunologyPurificationImmunoprecipitationLife SciencesELISACellRegulatory affairsTMFClinical DevelopmentRegulatory submissionsRegulatory RequirementsRegulatory Compliance

Skills and Expertise

Self Assessment :
Build and manage the Trial Master File (TMF) Analyze data Monitor a clinical studyAssist study siteBuild trial master file (TMF)Clinical data collectionArchive documentationManage clinical trial files/documentsMonitor clinical trials Organise meetingsRegulatory documentationRegulatory submissions


  • MSc in Biochemistry from University of Calcutta in 2011
  • Class 12 in Science from Better High School in 2006

Training and Certification

  • National Eligibility Test in 2011 Certification


BrightOwl Assessment:
Self Assessment:
Professional Proficiency

Area / Region

Aachen, Germany


Driving License
  • No

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