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Clinical Manager Job Title: Clinical Manager Qualification: Bachelors degree or equivalent qualification in Healthcare Experience: 3 years of experience is must. Skills Required: Fluent English ...
marketing accounts businessdevelopment insurance sales casestudies drugdevelopment clinicalpractices clinicaltrial apt basic design resume english training clinical management communication uccessSt ies WhiteP272560BR Medical Safety Writer- Aggregate Reporting Job Description 1. Lead preparation of global periodic safety reports for newly launched products. 2. Lead coordination with GLFs to ensure infor...
standardoperatingprocedures dataanalysis drugdevelopment projectmanagement qualityimprovement medicalterminology qc ar ars gcp sound medical writing english strategy analysis egulat ywriting rep ting templat
Lead the team of subject matter expert from GDD QMS who advise on training and process documents standards throughout the document and training lifecycle management process. Oversee the design, im...
globaldrugdevelopment standardoperatingprocedures environmentalimpactassessment qualitymanagementsystem qualitysystems changerequests processtraining drugdevelopment impactassessment ualitymanagementsystems
277055BR
Lead Consultant BPRJob Description
improved overall business and technology performance, Lead cross-divisional transformative projects as assigned, lea...
sap environment delivery customerrelations sales leansixsigma globaldrugdevelopment sixsigma processmapping designthinking computerscience specialprojects drugdevelopment dataarchitecture ateliais
276979BR
Narrative WriterJob Description
Your responsibilities include, but are not limited to:
1. Independently write and QC/review patient narratives.
277064BR
Principal Clinical Data ManagerJob Description
Your responsibilities:
Your responsibilities include, but are not limited to:
1. Provides Data Mana...
Familiarity with drug development life cycle and excellent skills with the manipulation, analysis and reporting of clinical trials data Ability to effectively perform complex statistical programming...
lifecycle clinicaltrials workeffectively drugdevelopment communicationskills statisticalprogramming sdtm adam trials english analysis clinical reporting communication ClinicalTrialManagementSystem lectronicDa1. Provides expert safety input to the clinical development program for assigned projects/ products and be an active member of the Global Program Team (GPT), Global Clinical Team (GCT) and Clinical Tr...
rec sharedservices issuemanagement drugdevelopment tatementsofw ksow globaldrugdevelopment healthcareprofessionals edata lifecycle dkeeping patientsafety graduatelevel englishlanguage safetServes as the Clinical Pharmacology representative on assigned studies. Provides Clinical Pharmacology support for product defense and maintenance activities for addressing regulatory queries and lab...
modeling simulation drugdevelopment commercialmodels clinicalpharmacology legislativerelations maintenanceactivities pharmaceuticalsciences qualemploymentopp tunityClinical Manager Job Title: Clinical Manager Qualification: Bachelors degree or equivalent qualification in Healthcare Experience: 3 years of experience is must. Skills Required: Fluent English ...
marketing accounts businessdevelopment insurance sales casestudies drugdevelopment clinicalpractices clinicaltrial apt basic design resume english training clinical management communication uccessSt ies WhitePDefine, design, and implement network communications and solutions within a fast-paced, leading edge database/applications company. Perform performance trend analysis and manage the server/network cap...
unixshellscripting softwaredevelopmenttools applicationmanagementservices lifecycle webservices itoperations systemdesign Windows Linux UNIXshellscripting computerscience drugdevelopment iebelDevOpsAdministrat
Lead the team of subject matter expert from GDD QMS who advise on training and process documents standards throughout the document and training lifecycle management process. Oversee the design, im...
globaldrugdevelopment standardoperatingprocedures environmentalimpactassessment qualitymanagementsystem qualitysystems changerequests processtraining drugdevelopment impactassessment ualitymanagementsystems
273493BR
Principal BiostatisticianJob Description
The Principal Biostatistician is responsible for all statistical work, scientific and operational, for one or more ...
statisticalanalysisplans drugdevelopment softwarepackages presentationskills bayesianstatistics statisticalanalysis protocoldevelopment statisticalsoftware statisticalconcepts tatementsofw ksow effectiv
276978BR
Global Program Regulatory Manager-LCMJob Description
Your responsibilities include, but are not limited to:
Responsible for implementing regulator...
267808BR Associate Director Clinical Data Management Job Description Your responsibilities: Your responsibilities include, but are not limited to: 1. Selects, recruits, develops, manages, motivat...
advisory finance compliance reporting training pecialprojects teamspirit clinicaldatamanagement customerrelations linemanagement computerscience stafftraining clinicaldata datamanagement drugdevelopmentYour responsibilities: Your responsibilities include, but are not limited to: 1. Study level: a. Responsible for all statistical tasks on assigned trials, and perform these tasks independently s...
globaldrugdevelopment statisticalanalysisplans sharedservices therapeuticarea drugdevelopment softwarepackages bayesianstatistics statisticalanalysis protocoldevelopment tatementsofw ksow statisticals
277055BR
Lead Consultant BPRJob Description
improved overall business and technology performance, Lead cross-divisional transformative projects as assigned, lea...
sap environment delivery customerrelations sales leansixsigma globaldrugdevelopment sixsigma processmapping designthinking computerscience specialprojects drugdevelopment dataarchitecture ateliais
276979BR
Narrative WriterJob Description
Your responsibilities include, but are not limited to:
1. Independently write and QC/review patient narratives.
Job Description 1. Support/ lead end- to- end preparation of aggregate safety reports. 2. Support coordination with GLFs to ensure information received, analyzed and incorporated into ARs as per the ...
drugsafety drugdevelopment managementskills projectmanagement medicalterminology communicationskills operationalexcellence documentationpractices it qc ar pv ars gcp risk testing egulat ywritingFor Business / Trade Enquiries : 1800 4191 417 We at Mendine inspire you to take your ideas and talent to its outmost potential. Realizing the seriousness of our field, we believe that whatever comes...
pharmaceuticalindustry asm business enquiries compromise MarketAccess Pharmaceutics HospitalSales PharmaceuticalSales SalesEffectiveness ClinicalDevelopment MedicalAffairs DrugDevelopment Pharmacovigilance luste252975BR Senior Clinical Programmer Job Description Position Purpose The Senior Clinical Programmer is responsible for all statistical programming aspects of assigned studies or project- level a...
lifesciences qualitycontrol datastructures sharedservices clinicaltrials computerscience drugdevelopment statisticalanalysis tatementsofw ksow globaldrugdevelopment phasei negotiationskills projJob Description 1. Serves as senior medical adviser to the SDC Head, and as point contact for any medically related matters impacting local SDC product development. Draws upon the full resource of th...
finance sales accountancy mis ltd eg medicalaffairs sharedservices localdevelopment therapeuticarea keyperformanceindicators drugdevelopment clinicaloutcomes clinicaltrials issueresolution medicalofficeBioinformatician Level 1: Bachelors in Biotechnology or Bioinformatics, with an outstanding academic record. ,...
biotechnology Biopharmaceuticals DrugDevelopment DrugDiscovery MonoclonalAntibodies Genomics AssayDevelopment IND Biomarkers Immunoassays ioinf maticsJob Title: Team Lead- Drug safety Location: Mysore, India Years of Experience: 4 to 5 Years of industry related experience Education: BPharm / Mpharm / Any equivalent degree Essential Duties and R...
msofficetoolsmsofficedrugsafetylifesciencesdrugdevelopmentinterpersonalskillsoliciesproceduressubjectmatterexpertisestronginterpersonalskillsfollowingupalcommunicationpresentationskillsCandidate should have minimum of 3 to 6 years of experience in SAS programming with relevant experience in managing EDC ( RAVE / Inform ) trials. Has good knowledge of the clinical drug development pr...
analyticsinformintellectualoffersportfolioharnessclinicalplsqlsciencehealthcareatasciencescientificdatamanagementadvancedanalyticssasprogrammingdrugdevelopment"
272560BR Medical Safety Writer- Aggregate Reporting Job Description 1. Lead preparation of global periodic safety reports for newly launched products. 2. Lead coordination with GLFs to ensure infor...
standardoperatingproceduresdataanalysisdrugdevelopmentprojectmanagementqualityimprovementmedicalterminologyarsgcpsoundmedicalwritingenglishstrategyanalysisegulatywritingreptingtemplatSenior Statistical programmer Job Description Your responsibilities: Your responsibilities include, but are not limited to: 1.Lead statistical programming activities as Trial Programmer for phase ...
programmingcompliancetatisticalanalysisplansdrugdevelopmentdatastructuresqualitycontrolstatementsofworksownegotiationskillsprocessimprovement267808BR Associate Director Clinical Data Management Job Description Your responsibilities: Your responsibilities include, but are not limited to: 1. Selects, recruits, develops, manages, motivat...
advisoryfinancecompliancereportingtrainingpecialprojectsteamspiritclinicaldatamanagementcustomerrelationslinemanagementcomputersciencestafftrainingclinicaldatadatamanagementdrugdevelopment273733BR Medical Safety Lead Job Description 1. Monitors the clinical safety of projects/ products including activities such as literature review, evaluation of individual cases or signal detection...
riskmanagementplanshealthcareprofessionalsmedicalreviewpatientsafetyriskmanagementdatamanagementmedicalaffairsdrugdevelopmentclinicaldevelopmentdataregulatyaffairsregulatyrequirementsServes as the Clinical Pharmacology representative on assigned studies. Provides Clinical Pharmacology support for product defense and maintenance activities for addressing regulatory queries and lab...
modelingsimulationdrugdevelopmentcommercialmodelsclinicalpharmacologylegislativerelationsmaintenanceactivitiespharmaceuticalsciencesqualemploymentopptunityJob Title : Associate Team Lead- Drug safety Location: Mysore , India Years of Experience: 3 to 4Years of industry related experience in Pharmacovigilance / Pharmaceutical Education: BPharm / Mphar...
msofficetoolsmsofficedataentrydrugsafetylifesciencesdrugdevelopmentoliciesproceduressubjectmatterexpertisestronginterpersonalskillsfollowingupalcommunicationpresentationskillsinterp250232BR Senior Analyst - Database Operation Job Description 1.Entry Level knowledge in Oracle Clinical and EDC systems like INFORM, RAVE etc. and also carries basic understanding of SDTM. 2.Work w...
basisaccountsresearchdatamanagementproblemsolvingclinicaltrialsdrugdevelopmentprojectmanagementcommunicationskillsustomerrelationsreptingthirdpartyvendacleclinicalmedicalterminologyExperience: 5 - 7 Years of Indistry expereience (3 years experience in Pharcovigilance) Qualification: MBBS/ MD Essential Duties and Responsibilities: As an Associate Project Manager Supervision...
documentationustomerrelationsdrugdevelopmentmsofficeprojectmanagementstronginterpersonalskillsfollowingupsubjectmatterexpertiseJob Description 1. Serves as senior medical adviser to the SDC Head, and as point contact for any medically related matters impacting local SDC product development. Draws upon the full resource of th...
financesalesaccountancymisltdmedicalaffairssharedserviceslocaldevelopmenttherapeuticareakeyperformanceindicatorsdrugdevelopmentclinicaloutcomesclinicaltrialsissueresolutionmedicalofficeThe incumbent shall liaise with stakeholders in Sandoz Development Centre PD project team for Root Cause Analysis, conduct review and facilitate on time closure of Non - conformances, Change requests,...
testcasesregressiontestingautomationrootcauseanalysissharedservicesdrugdevelopmentqualityunctionalrequirementscontinuousimprovementfacilitationrootcausewatertestingbatchrecchangerequests1. Provides expert safety input to the clinical development program for assigned projects/ products and be an active member of the Global Program Team (GPT), Global Clinical Team (GCT) and Clinical Tr...
recsharedservicesissuemanagementdrugdevelopmenttatementsofwksowglobaldrugdevelopmenthealthcareprofessionalsedatalifecycledkeepingpatientsafetygraduatelevelenglishlanguagesafet270806BR Solution Design Exp Advanced Analytics Job Description Novartis is actively seeking a Solution Design Expert , Big Data and Advanced Analytics to join our analytics team focusing in the ar...
lifesciencescustomerfocusdatamanagementsharedservicessolutiondesigndrugdevelopmentdataarchitecturehirdpartyvendbigdataitservicesitdeliveryitprojectsfocalpointprojectteamssoluThe incumbent will be the lead development QA representative in the SDC (Sandoz Development Centre) PD project team. Provide guidance, quality compliance support, performs document approval, support t...
testcasestestscenariostestcasedesigntestexecutionenvironmentduediligenceproductlaunchsharedservicesdrugdevelopmentontinuousimprovementfacilitationwatertestingbatchrecleaddevelopment270812BR Solution Design Expert - Real World Evidence Job Description Novartis is actively seeking a Solution Design Expert , Real World Evidence RWE to join our analytics team focusing in the area...
lifesciencescustomerfocusdatamanagementsharedservicessolutiondesigndrugdevelopmentdataarchitecturehirdpartyvendsubjectmatterexpertisebigdataitservicesitprojectsfocalpointsolution252975BR Senior Clinical Programmer Job Description Position Purpose The Senior Clinical Programmer is responsible for all statistical programming aspects of assigned studies or project- level a...
lifesciencesqualitycontroldatastructuressharedservicesclinicaltrialscomputersciencedrugdevelopmentstatisticalanalysistatementsofwksowglobaldrugdevelopmentphaseinegotiationskillsproj255992BR Pharmacovigilance Leader Job Description 1.Acts as the primary contact point with PVE in HYD , CSS and co-ordinates product-specific activities. 2.Performs medical review of individual SAE...
sharedservicesclinicaltrialsissuemanagementdrugdevelopmentlobaldrugdevelopmenthealthcareprofessionalsmedicalreviewpatientsafetyresearchmanagementregulatyrequirementsclinicaltrialsignaldeteAssociate Director Innovative Technologies & Products with Minimum 10 -12 years of experience in developing products on NDDS platform for local & global markets Ferring India is looking for a ...
techprojectmanagementsalesgmpbasismanufacturingmanagementindustryhealthresearchbusinessdevelopmentprogrammanagementsopsdrugdevelopmentrepYour responsibilities: Your responsibilities include, but are not limited to: 1.Support development of early and late phase NCE development for solid dosage forms (including poorly soluble compoun...
validationhplcsopdocumentationprotocolssharedservicesdrugdevelopmentransfertoproductionglobaldrugdevelopmentinfmationsecuritystandardscontinuousimprovementfacilitationprocesstransfersecurityresear268162BR Associate Director PPM Governance - Ops Job Description Design and apply quality checks ensuring Drug Development process and project plans are done according to approved processes. Intera...
complianceadvisoryfinancereportingrojectplansdataflowcustomerrelationssharedservicesrecordofsuccessdataqualitylifesciencestimemanagementprojectmanagersglobaldrugdevelopmentdrugdevelopment267808BR Associate Director Clinical Data Management Job Description Your responsibilities: Your responsibilities include, but are not limited to: 1. Selects, recruits, develops, manages, motivat...
advisoryfinancecompliancereportingtrainingpecialprojectsteamspiritclinicaldatamanagementcustomerrelationslinemanagementcomputersciencestafftrainingclinicaldatadatamanagementdrugdevelopment256009BR Expert , Systems Operations - Reporting Job Description 1. Act as deputy for Head Systems Operation Reporting and Submissions 2. Manage / supervise / coach / train / assist and mentor: - (...
drugsafetydatamanagementsharedservicescaseprocessingdrugdevelopmentdatabaseadministrationlobaldrugdevelopmenteuropeanwkscouncilssassqlpatientsafetytherapeuticareassystemoperations263811BR Head Clinical Analytics Job Description The Global Head , Clinical Analytics is responsible for defining and executing data and analytics strategies in a dynamic environment and in support...
dataanalyticssharedservicescomputersciencedrugdevelopmentmanagementdhocreptingglobaldrugdevelopmentpeoplemanagementskillspowerbiqliksensemusicmakingdatareptingcustomercentricvend© 2019 Hireejobs All Rights Reserved