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PRIMARY PURPOSE : The Director, Biostatistics (India) provides statistical support for clinical research projects including developing and overseeing statistical deliverables, providing guidanc...
corporate quality assurancestandard operating procedureslead changework processesdata managementproblem solvingsas programmingexternal clientsquality assuranceclinical researchstatements of work sow
Any Graduate/ Post Graduate with 1- 2 years of IT experience in Java and related areas with SQL knowlegde in any of the databases We prefer enthusiastic learners willing to adapt to new and demanding...
fdaedctroubleshootingcdmsqljavadata managementsql servermanagement servicesmanagement systemclinical triallaboratory information management systeminformation managementIgnore Email If do not suits your requirenment Client: One of the Pharma Company Designation :Sr. Officer – DRA DCGI Location : Mumbai Candidates who is willing to relocate to Mumbai Can als...
web browsingweb chatmobile switching centre serverplanningdiameterdcgipharmachatdesignationprotocolshsspgwsgsnvoltedeep packet inspectiononline supportdradibelsemailpolicy charging rules functionPRIMARY PURPOSE : The Director, Biostatistics (India) provides statistical support for clinical research projects including developing and overseeing statistical deliverables, providing guidanc...
corporate quality assurancestandard operating procedureslead changework processesdata managementproblem solvingsas programmingexternal clientsquality assuranceclinical researchstatements of work sowGood understanding of regulatory framework, including regional trends, for various types of applications and procedures for small and large molecules across all regions as well as knowledge of global ...
clinical trialsdocumentationapacdcgisopmanagement systemmanagement systemsworking experiencelegislative relationsinformation managementichveevavaultsciencecmcPRIMARY PURPOSE : The Director, Biostatistics (India) provides statistical support for clinical research projects including developing and overseeing statistical deliverables, providing guidanc...
corporate quality assurancestandard operating procedureslead changework processesdata managementproblem solvingsas programmingexternal clientsquality assurancestatements of work sowGood understanding of regulatory framework, including regional trends, for various types of applications and procedures for small and large molecules across all regions as well as knowledge of global ...
clinical trialsdocumentationapacdcgisoplife sciencesmanagement systemmanagement systemsworking experiencelegislative relationsinformation managementichveevacmcRoles and Responsibilities You will be based at a Corporate office at Mumbai. You will be responsible for, 1. Candidate will be responsible for Prepare registration dossier for pro...
artworkstatutoryabbreviated new drug applicationdraftingdcgielectronic common technical documentbranch officesregulatory affairsregulatoryregistrationregulatory submissionsgeneric programmingpackagingcolordocumentationclarifycosmeticsWorks effectively within a team environment but may work independently delivering services within their area of competence Works within broad project guidelines as directed by the project lead and/or ...
soprisk identificationdocumentationproject planningtrainingapacclient contactinvoicingalignmentclinical trialscontroldcgiprovisionplanningfinancialscompliancesite initiationlife sciencesriskproject setupIt is planned to select 3 awarded AZ projects that serves as Pilot projects with different filing requirements (PMED, Veeva-Vault) or were submission has been done via VHP. After completion of the pil...
clinical trialsdocumentationapacdcgisoppilot projectsfilingcompletionPilot PlantProof of ConceptMembrane SeparationsInstrument Rated PilotMembraneDesalinationReverse Osmosis
Good understanding of regulatory framework, including regional trends, for various types of applications and procedures for small and large molecules across all regions as well as knowledge of global ...
clinical trialsdocumentationapacdcgisopmanagement systemmanagement systemsworking experiencelegislative relationsinformation managementichveevavaultplanningauthoringmanagementregulatorymaintenancecmc -
Any Graduate/ Post Graduate with 1- 2 years of IT experience in Java and related areas with SQL knowlegde in any of the databases We prefer enthusiastic learners willing to adapt to new and demanding...
fdaedctroubleshootingcdmsqljavadata managementsql servermanagement servicesmanagement systemclinical triallaboratory information management systeminformation managementLocation: Gurgaon State: Haryana PostalCode: 122002 Recruiter: nidhi Chakhaiyar - +91 92657 23772 Qualifications: documentationclarifycolorcosmeticsdraftingsenior managementartdcgieasepharmaimportbusinessplanninganalysismanagementregulatoryaffiliatesformulationpreparationmedical
Roles and Responsibilities You will be based at a Corporate office at Mumbai. You will be responsible for: Product Launch
Any Graduate/ Post Graduate with 1- 2 years of IT experience in Java and related areas with SQL knowlegde in any of the databases We prefer enthusiastic learners willing to adapt to new and demanding...
fdaedctroubleshootingcdmsqljavadata managementsql servermanagement servicesmanagement systemclinical triallaboratory information management systeminformation management -
Regulatory Affairs- Job description: Regulatory Affairs Specialists assist in obtaining and maintaining government approval for drugs, medical devices, nutritional products, and related materials. T...
sopapacclinical trialsdocumentationdcgiRegulatory Affairs- Job description: Regulatory Affairs Specialists assist in obtaining and maintaining government approval for drugs, medical devices, nutritional products, and related materials. T...
sopapacclinical trialsdocumentationdcgiRegulatory Affairs- Job description: Regulatory Affairs Specialists assist in obtaining and maintaining government approval for drugs, medical devices, nutritional products, and related materials. T...
sopapacclinical trialsdocumentationdcgiRegulatory Affairs- Job description: Regulatory Affairs Specialists assist in obtaining and maintaining government approval for drugs, medical devices, nutritional products, and related materials. T...
sopapacclinical trialsdocumentationdcgiDesignation: Clinical Research Manager Reports to: Director Industry: Medical Devices (Class II & Class III Orthopedic Implants) Place of Posting: Sonepat 2 KM from NCR Del...
adverse eventsbudgetingacer hardwaresafetymedical writingclinical research associatesiso 14971protocol designingclinical researchcroexternal auditmedical device directiveclinical trialsqualityindividual developmentmedical devicesclinical p1. Work experience - Need 2-4 years of end to end publishing experience in US/EU and ROW countries. eCTD Submission Publishing with Canadian submissions will be added advantage. 2. Shift time - West c...
clinical trialsdocumentationapacdcgisopdigital conversionpharmaePubEbooksDigital PublishingContent ManagementPublishingDigital MediaEditingHTMLAdobe PhotoshopHealth Information ExchangeAny Graduate/ Post Graduate with 1- 2 years of IT experience in Java and related areas with SQL knowlegde in any of the databases We prefer enthusiastic learners willing to adapt to new and demanding...
fdaedctroubleshootingcdmsqljavadata managementsql servermanagement servicesmanagement systemclinical triallaboratory information management systeminformation management
-- Contributes to process improvements -- Typically resolves problems using existing solutions -- Provides informal guidance to junior staff -- Works with minimal guidance -- Requires in-depth knowled...
clinical trialsdocumentationapacdcgisopregulatory affairsinvestment researchlesspharmaresearchnetworkinginvestmentregulatoryretirementElectronic Common Technical DocumentRegulatory SubmissionsJob Details
Works effectively within a team environment but may work independently delivering services within their area of competence Must be able to work independently on submissions, mentor publishers and pro...
clinical trialsdocumentationapacdcgisopadobe acrobatmicrosoft officemanagement systemsdigital conversiondocument managementsoftware validationneeswindowsdesktopsoftwareadobeWorks effectively within a team environment but may work independently delivering services within their area of competence Must be able to work independently on submissions, mentor publishers and pro...
clinical trialsdocumentationapacdcgisopadobe acrobatmicrosoft officemanagement systemsdigital conversiondocument managementsoftware validationneeswindowsdesktopsoftwareadobeWorks effectively within a team environment but may work independently delivering services within their area of competence Must be able to work independently on submissions, mentor publishers and pro...
clinical trialsdocumentationapacdcgisopadobe acrobatmicrosoft officemanagement systemsdigital conversiondocument managementsoftware validationneeswindowsdesktopsoftwareadobeWorks effectively within a team environment but may work independently delivering services within their area of competence Must be able to work independently on submissions, mentor publishers and pro...
clinical trialsdocumentationapacdcgisopadobe acrobatmicrosoft officemanagement systemsdigital conversiondocument managementsoftware validationneeswindowsdesktopsoftwareadobe
Centre Head:
Work on post approval CMC activities. Licence Renewals, CMC and safety variations, MAA submissions, withdrawals etcQualificationsExperienced in CMC post approval submissions for EU, A...
soprenewalsmanagementinformation managementdcgidocument managementwithdrawalsclinical trialsapacdocumentationedrmsdocument captureliasingiprodocument imagingregulatorycmc
Location: Gurgaon State: Haryana PostalCode: 122002 Recruiter: nidhi Chakhaiyar - +91 92657 23772 Qualifications: documentationclarifycolorcosmeticsdraftingsenior managementartdcgieasepharmaimportbusinessplanninganalysismanagementregulatoryaffiliatesformulationpreparationmedical
A Graduate degree in a relevant educational field - Life Science, Pharmacy, Scientific or Technical Discipline. 0 to 6 months experience with Pharmaceutical industry or CRO with general understanding...
clinical trialsdocumentationapacdcgisopcommunication skillspharmaceutical industrycroctrsfilingscienceeducationregulatoryregulationscompilationcommunicationMarket AccessPharmaceuticsHospital SalesRegulatory Affairs- Job description: Regulatory Affairs Specialists assist in obtaining and maintaining government approval for drugs, medical devices, nutritional products, and related materials. T...
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