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* Manager, Global Medical Information and Scientific Affairs responsible for ensuring timely delivery of clinical trial disclosure documents and medical information responses for Global OTC products....
end to end deliverydevelopment of employeesrisk management frameworkstatistical analysis planskey performance indicatorsenvironmental impact assessmentdata sharingclinical datastatements of work sowWe are team of analysts, engineers, data scientists and designers building powerful intelligence tools for business users. Contify is a 360 degree market intelligence platform that enables businesses ...
life sciencesmarket researchcustomer servicebusiness researchclient managementpeople managementcorporate liaisonbusiness insightssecondary researchmarket intelligenceevidence collectionClarivate is a global leader in providing solutions to accelerate the lifecycle of innovation. Our bold mission is to help customers solve some of the world s most complex problems b...
clinical dataproject designsystematic approachresearch projectsheart failureprimary market researchtherapeutic areasecondary marketfinancial sectorstock exchangedata analyticsmarket researchClarivate is a global leader in providing solutions to accelerate the lifecycle of innovation. Our bold mission is to help customers solve some of the world s most complex problems b...
heart failureprimary researchmarket researchdata analyticsproject designmarket trendsexcelcommunication skillsprimary market researchstock exchangemicrosoft officesystematic approachclinical data
Position Responsibilities
Position Description Combine two of the fastest-growing fields on the planet with a culture of performance, collaboration and opportunity and this is what you get. Leading edge technology in an indus...
ushealthcare it medicalrecords reach compliance physiotherapy codes specialprojects planet cpt leap adr clinicaltrials managedcare claims mcProficiency in English with effective verbal written skills Candidates with experience will have preference Job Description Research Writing viz. protocol, case report form preparation etc Abstract,...
clinicaltrials safety protocols research literature adobecreativesuite medicomarketing researchwriting reportpreparation clinicaltrial medical writing english posters clinical protocol journals marketing egulator
This position will oversee all statistical aspects of assigned projects & be responsible for introducing and ing new methodology where appropriate. Statisticians serve as consultants to our ...
dataanalysis studyreports medicaldevices medicalwriting datamanagement datacollection problemsolving clinicaltrials sasprogramming projectmanagement strategicplanning clinicaloperations clientsatisfaction regulatoryagencies statisticalanalysClinical Research Associate Senior CRA with minimum 2 years in ICU. Must have references and latest ICH - GCP certificate,...
gcp clinicalresearch clinicaltrials documentation site cra ich research clinical MedicalEducation ClinicalMonitoring MedicalResearch ClinicalTrialManagementSystem ClinicalOperations InternalMedicine lectronReg Affairs & Reg Ops for pharma & vaccines: Lifecycle, Renewals, MRP, DCP Core packages Works effectively within a team environment but may work independently delivering services within their area o...
clinicaltrials documentation apac dcgi sop adobeacrobat microsoftoffice insightpublisher managementsystems digitalconversion documentmanagement softwarevalidation mrp dcp dobeYour responsibilities include, but are not limited to: In collaboration with Global Head of Data Operations, Data Operations Leadership Team and Leadership Teams of partner GDO functions, defining th...
problemsolving clinicaltrials timemanagement linemanagement computerscience strategicgrowth strategicvision drugdevelopment managementskills projectmanagement igitalinnovationoperationsleadershipMedical Writer Pharmacists , physicians , and life science graduates having medical writing experience,...
clinicaltrials safety protocols research literature medicalwriting writing science MedicalCommunications PublicationPlanning MedicalAffairs Abstracts ContinuingMedicalEducation MedDRA PSUR PSURs InvestigatorBrochures MedicalEducation IntRequired Clinical Researchers Experience: 0-1 years Qualification: BDS, Physiotherapy, Pharmacy, Nursing, Any Life Science graduates Post Graduates ,...
clinicaltrials businessdevelopment clinicaldatamanagement compliance crf nursing science clinical physiotherapy NursingEducation NursingProcess MedicationAdministration AcuteCare edicalSurgical NursingDocumenta
Essential Duties and Responsibilities:
As a Medical Reviewer
Essential Duties and Responsibilities: As a Medical Reviewer
Essential Duties and Responsibilities: As a Medical Reviewer
As part of the Data Monitoring and Management group, an integral delivery unit within the Global Biometrics and Data Management (GBDM) organization, the Data Manager is responsible for timely and high...
dataentry datamanagement research datacollection programming equalemploymentopportunity clinicaldata datacleaning clinicaltrials databasedesign datamonitoring tatementsofworksowSALARY: 3 Lakhs VACANCIES: 1 QUALIFICATION: Any Graduate MALE/FEMALE: Male/Female EXPERIENCE: 1 Year to 5 Years JO...
gcp clinicalresearch clinicaltrials documentation site datacollection communicationskills verbalcommunication tamil forms research clinical briefing materials numerical healthcare recruitment instructions communication edicalPharma Professional who has sound knowledge of Clinical Trial Site Monitoring Creation & Development of Essential Clinical Trial Documents, Clinical Trial Site Selection, Monitoring.,...
gcp clinicalresearch clinicaltrials documentation site siteselection clinicaltrial sound pharma clinical monit TenantRepresentation RetailSiteSelection InvestmentSales CCIM itemonit ing ing ShoppingCenter1. Provide input as required at all meetings, discussions and activities covering aspects of Statistical Reporting on trial level activities. 2. As required, make certain that documents and specifica...
sas sasprogramming sdtm datamanagement reporting phasei clinicaltrials computerscience statisticalreporting summarizinginformation clinicaltrial tatementsofworksowThe position as Senior Group Head, Data Management is an influential leader within Data Operations in ensuring that device and drug-development plans in Novartis are executed efficiently with timely a...
clinicaldatamanagement teamspirit clinicaldata timetracking datacleaning stafftraining datamanagement clinicaltrials linemanagement teamleadership computerscience tatementsofworksowClinical Research Associate Senior CRA with minimum 2 years in ICU. Must have references and latest ICH - GCP certificate,...
gcp clinicalresearch clinicaltrials documentation site cra ich research clinical MedicalEducation ClinicalMonitoring MedicalResearch ClinicalTrialManagementSystem ClinicalOperations InternalMedicine lectronClinical Study Director (CSD) Job Details: This role is key for medical supervision and medical management of clinical trials proposed or to be performed by the Clinical Science Operations Platform (...
csd science management operations supervision clinicaltrials rials medical business clinical medicalmanagement clinicalstudy
Job Description Review of study Protocol, CRF, ICF, Subject questionnaire and its compliance with regulatory Cross checking of IEC summary reports, Investigators brochures and clinical reports a...
Job Description Understanding SDTM models and mapping different clinical data to suitable SDTM domains based on the latest implementation guidelines Working in SAS Base and SAS MACRO, Pharma dom...
Job Description Review of study Protocol, CRF, ICF, Subject questionnaire and its compliance with regulatory. Cross checking of IEC summary reports, Investigators brochures and clinical reports ...
Job Description Medical Reviewer Job Responsibilities Keeping track of updates of the drug and cascade to drug safety, pharmacovigilance into clinical trials. Communication and discussion with t...
CDR - L9 & L10 - Bengaluru 4.0 Year(s) - 9.0 Year(s) CDR L9 L10 Bengaluru Bengaluru/Bangalore :Stalwart Management Consulting CDR - L9 & L10 - Bengaluru Job Openings Details Stalwart Management Cons...
dataquality lifesciences datacleaning clinicaltrials impactanalysis managementconsulting cdm education management linicaldata cdr acle trials streams analysis database clinical openings protocol rep tingRare Conditions is part of the PI portfolio, and the new Infinity model for RC is spearheading the overall transformation within PI. The transformation aims to create a more innovative organization th...
integrateddevelopmentenvironments marketaccess clinicaltrials medicalaffairs drugdevelopment financialplanning clinicaloperations competitivelandscape pi eco map fit sma ateliaison teamcollab ationMedical review of the ICSRs (clinical, spontaneous, Drug surveillance, literature and spontaneous) adhering to SOP designed by client. Keeping track of updates of the drug and cascade to drug safety, ...
filing programming quality sla sop drugsafety medicalreview clinicaltrials it bpo dra ites ecrf pharma design trials cascade training drafting edicalMedical review of the ICSRs (clinical, spontaneous, Drug surveillance, literature and spontaneous) adhering to SOP designed by client. Keeping track of updates of the drug and cascade to drug safety, ...
filing programming quality sla sop drugsafety medicalreview clinicaltrials it bpo dra ites ecrf pharma design trials cascade training drafting edical
Execute and manage ad-hoc research requests (Disease burden analysis, Market Assessment/landscape, Competitive Analysis, Product and Company Profiling, Industry Analysis, KOL Mapping, Clinical tri...
socialmedia dataanalysis clinicaltrials companyprofiling industryanalysis competitiveanalysis compatibilitytesting databaseadministration it sas kol ims oracle design trials research analysis database clinical dobe
Execute and manage ad-hoc research requests (Disease burden analysis, Market Assessment/landscape, Competitive Analysis, Product and Company Profiling, Industry Analysis, KOL Mapping, Clinical tri...
socialmedia dataanalysis clinicaltrials companyprofiling industryanalysis competitiveanalysis compatibilitytesting databaseadministration it sas kol ims oracle design trials research analysis database clinical dobe Pulmonologist Level : Jr
Qualification : DNB Pulmonology Experience : 2 to 6 Yrs
Type : Clinical Number of Openings: 1 ,...
Job Description Medical review of the ICSRs (clinical, spontaneous, Drug surveillance, literature and spontaneous) adhering to SOP designed by client. Keeping track of updates of the drug and ca...
Required Clinical Researchers Experience: 0-1 years Qualification: BDS, Physiotherapy, Pharmacy, Nursing, Any Life Science graduates Post Graduates ,...
clinicaltrials businessdevelopment clinicaldatamanagement compliance crf nursing science clinical physiotherapy NursingEducation NursingProcess MedicationAdministration AcuteCare edicalSurgical NursingDocumentaProvide Clinical data management support to Clinical Operations team and/or study project, Clinical Data Management team and Biostatistics team. Participates in the review of Clinical research docume...
clinicaltrials clinicaldatamanagement case research management operations statisticalanalysis design protocols clinicalresearch datamanagement ms suppAbout Novotech: Novotech is internationally recognised as the leading independent and full-service contract research organisation (CRO) in the Asia Pacific region. We provide a wide range clinical de...
operationteam clinicaltrial bonus pharmaceuticalindustry contractreview phasei iv cro businessdevelopment microsoftoffice excel clinicaltrials analyticalresearch processimprovement set clinicaldevelopment therapeuticareas lifesciences soLooking for SDTM Programmer in Mumbai #Jobs Job Description We are looking for an associate with at least 8+ years of experience for SDTM position at mumbai, having strong understanding and experien...
basesas sasbase clinicaldata clinicaltrials cdiscstandards statisticalanalysis sas sdtm turn macro pharma trials analysis clinical management communication implementation PWS Deliverables tatementsofworksowJob Description We are looking for an associate with at least 8+ years of experience for SDTM position at mumbai, having strong understanding and experience of SDTM creation as per CDISC standards an...
basesas sasbase clinicaldata clinicaltrials cdiscstandards statisticalanalysis sas sdtm macro pharma trials analysis clinical management communication implementation PWS Deliverables SourceSelection tatementsofworksowEssential Duties and Responsibilities: As a Medical Reviewer
Essential Duties and Responsibilities: As a Medical Reviewer Conduct review and assessment of individual case safety reports obtained from clinical trials, spontaneous and solicited reports Dete...
drugsafety safety case compliance gvp stronginterpersonalskills lifecycle lifesciences globalhealth medicalreview adverseevents teammanagement clinicaltrials peoplemanagement oliciesprocedures prod
Essential Duties and Responsibilities:
As a Medical Reviewer
Essential Duties and Responsibilities:
As a Medical Reviewer
Location:Bengaluru Area, India Qualification: B. Pharma / M. Pharmacy / M.Sc., 4 - 10 years of Experience in CRO (BA BE centre Clinical Trials/ pharma is preferred. Responsible Promoting ICBios cli...
milestones iii marketing cro business pharma proposals pipelines research management trials clinical linicaltrial paymentcollection competitiveintelligence clinicaltrials clinicalresearch businessdevelopmentEssential Duties and Responsibilities: As a Medical Reviewer Conduct review and assessment of individual case safety reports obtained from clinical trials, spontaneous and solicited reports Dete...
safety case drugsafety gvp lifesciences teammanagement clinicaltrials ep ting policiesprocedures peoplemanagementskills stronginterpersonalskills lifecycle globalhealth medicalreview adverseevents© 2019 Hireejobs All Rights Reserved