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Summary

highly resourceful and personable medical professional with 4+ years of experience supervising and monitoring a large Phase III Clinical Trial, 2 years in managing epidemiological studies and 1.5 years as a clinician. currently a PhD Candidate with excellent Communication Skills, ability to work independently as well as in a team, and extensive project knowledge from concept to execution. trained in Good Clinical Practice, data collection, processing and Analysis; and, Bioinformatics computation. 

 

Experiences

Current Experience

  • Doctoral Research Assistant

    Toledo, OH, USA
    Since August 2013
    • used Perl to design and execute computer Algorithms and used ‘r’ for Data Analysis.
    • characterized and catalogued snp haplotypes to study human evolution from the 1000 genome data.
    • authored manuscripts and abstracts for scientific journals, prepared presentation materials (scientific poster, power-point).
    • Teaching assistant in graduate level course ‘introduction to Bioinformatics computation’ in spring - 2016 and 2017
    • Used Perl to design and execute computer algorithms and used ‘R’ for data analysis.
    • Characterized and catalogued SNP haplotypes to study Human evolution from the 1000 Genome data.
    • Authored manuscripts and abstracts for scientific journals, prepared presentation materials (scientific poster, power-point).
    • Teaching assistant in graduate level course ‘Introduction to Bioinformatics Computation’ in Spring - 2016 and 2017

Past Experience

  • Project Manager (SRF) Kolkata, West Bengal, India

    August 2011 --- June 2013
    • designed and managed ‘Health situation assessment’ project in sunderbans, india.
    • provided effective Leadership to project staff in the field level and organized the data-management process.
    • actively contributed in preparation and review of project report and ensured accuracy and timeliness to all collaborators.
    • developed project proposals and reports for studies of the division of Epidemiology, niced (icmr), kolkata, india.

  • Research Scientist Kolkata, West Bengal, India

    June 2010 --- December 2010
    • supervised the Phase III randomized controlled trial of bivalent killed whole-Cell oral cholera vaccine conducted in collaboration between niced (icmr), kolkata, india and international vaccine institute, seoul, south korea.
    • comprehensively managed 40+ medical personnel and 100+ non-medical personnel with superior conflict resolution.
    • coordinated regulatory activities, internal monitoring & quality reviews, and periodic internal self-audit of records.
    • contributed to Strategic Planning for effective disease surveillance which resulted in higher case detection.
    • overseen Data entry and Validation and ensured accuracy, integrity and Compliance of data collection process.
    • trained 40+ medical personnel and 100+ non-medical personnel on ich-gcp, project protocols and sops.
    • reviewed crfs and provided oversight and guidance as needed to Research staff.
    • evaluated and resolved study related issues and communicated periodically to investigators and sponsors.
    • served as the primary liaison between the pi and local physicians and government agencies.
    • ensured adherence to standard operating procedures (SOP), Good Clinical Practice (ich-gcp) and other project regulations.

  • Medical Supervisor Kolkata, West Bengal, India

    November 2006 --- May 2010
    • supervised the Phase III randomized controlled trial of bivalent killed whole-Cell oral cholera vaccine conducted in collaboration between niced (icmr), kolkata, india and international vaccine institute, seoul, south korea.
    • comprehensively managed 40+ medical personnel and 100+ non-medical personnel with superior conflict resolution.
    • coordinated regulatory activities, internal monitoring & quality reviews, and periodic internal self-audit of records.
    • contributed to Strategic Planning for effective disease surveillance which resulted in higher case detection.
    • overseen Data entry and Validation and ensured accuracy, integrity and Compliance of data collection process.
    • trained 40+ medical personnel and 100+ non-medical personnel on ich-gcp, project protocols and sops.
    • reviewed crfs and provided oversight and guidance as needed to Research staff.
    • evaluated and resolved study related issues and communicated periodically to investigators and sponsors.
    • served as the primary liaison between the pi and local physicians and government agencies.
    • ensured adherence to standard operating procedures (SOP), Good Clinical Practice (ich-gcp) and other project regulations.

  • House Physician Kolkata, West Bengal, India

    April 2006 --- October 2006
    • provided comprehensive medical care to in-patients and outpatients.
    • orchestrated Operations of osteo-arthritis clinic.

Personality

Self Assessment :
AdaptabilityAnalytical thinkingApproachabilityAttention to detailAuthenticityCollaborationCommunicativeCoordinationCreative thinkingCritical thinkingDependabilityDiligenceEfficiencyFlexibilityIndependenceInnovative thinkingInterest in knowledgeOrganizationProactivityProblem solvingResiliencyResponsibilityResult OrientedSelf-confidenceSelf-disciplineSociabilityTrustStrategic thinking

Knowledge

Self Assessment :
Diabetes Phase I R&D Scientific writingAnalysisBioinformaticsBiomedical SciencesBiological Drug DevelopmentCardiovascular diseasesClinical researchClinical Study DesignClinical trial designClinical trial management Lab scale batches Cell biologyCRFCRF designData AnalysisData ManagementDatabasesDrug DevelopmentEndocrinology and metabolismEpidemiologyGood Clinical Practice (GCP)HealthcareHospitalsHuman AnatomyInformed Consent ProcessInformed Consent DocumentsLife SciencesmanagementMedicineMicrosoft OfficeMicrosoft PowerpointMicrosoft ExcelMicrosoft WordMolecular & Cellular Biologypeople managementPerlPhase IIIPhases of clinical development (phase I to IV)Problem SolvingProject ManagementProtocolReport WritingResearchScientific Writing

Skills and Expertise

Self Assessment :
Analyze data Develop clinical trial protocols Design case record forms Interact with physicians Monitor a clinical study Search literature on clinical trialsAnalyze data/information to determine potential relationships.Approve consent documentsApprove patient informationAssist with site trainingAttend seminarsAttend seminars, courses and meetings within and outside the companyBiomarker ResearchCoach staffCollaborate with project teamCollect dataCollect financial data from hospitalsCollect patient forms and questionnairesCommunicate effectively on different company levelsCollaborate with medical teamCommunicate with investigatorCoordinationData validationData miningDesign case record form (CRF)Design clinical presentationDesign scientific experimentsDesign scientific projects (in biology)Design studiesDetermine potential relationshipsDevelop training materialsExecute scientific projectsInformed consent processInteract with KOLInteract with physiciansInterpret scientific dataInterpret research resultsLiaise with doctorsLiaise with doctors and other professionals throughout the studyLiaise with research teamLiaise with research team in order to accurately collect and record dataMaintain strong relationshipsManage research projectsNetworkProvide medical insightsProvide trainingPublication of articlesRead medical literature to maintain current awareness and knowledgeResearch at universitiesReview informed consent processReview study protocolsSupervise data processingTeach university studentsTrain on site staffUnderstand protocolsVerify dataWork collaboratively with the other members of the clinical research team Work cross-functionallyWrite documentsWrite papers

Education

  • Ph.D. in Biomedical Sciences from University of Toledo in 2017
  • Bachelor in Medicine from NRS Medical College in 2006

Training and Certification

  • Advance Vaccinology Course in 2010 Training
  • Good Clinical Practice in 2016 Certification
  • Good Clinical Practice in 2009 Certification

Languages

BrightOwl Assessment:
Self Assessment:
English
Full Proficiency
BENGALI
Native
Hindi
Full Proficiency

Work Preferences

  • Notice Period:
    9 weeks
  • Positions I am interested in:
    Medical Science Liaison (MSL) Clinical Research Associate (CRA) Clinical Project Manager (CPM) Scientist Assistant Professor Medical Writer associate Clinical Project Manager Post-doctoral Fellow
  • Work From Home:
    Yes, 0 to 1 days per week
  • Work Regime:
    Permanent position
  • International:
    Yes

Publications

    Expert has 4 publications (Will be avalible with full profile)

Area / Region

United States

Others

Driving License
  • Yes

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