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Perform QC checks of draft protocol, draft CRF, draft ICF and other study related requirements. Observing the pre-check-in, check-in, pre-dose, dosing, post-dose activity as per protocol, SOP/IOPs reg...
baggagehandlingsystems validationreports clinicaldevelopment regulatoryguidelines qc crf ria tmf visit labels checks clinical protocol equipment regulatory monitoring validation completion calibration cfPerform QC checks of draft protocol, draft CRF, draft ICF and other study related requirements. Observing the pre-check-in, check-in, pre-dose, dosing, post-dose activity as per protocol, SOP/IOPs reg...
baggagehandlingsystems validationreports clinicaldevelopment regulatoryguidelines qc crf ria tmf visit labels checks clinical protocol equipment regulatory monitoring validation completion calibration cfYour responsibilities include, but are not limited to: Responsibility for ensuring high quality clinical trial data review/insights and analysis as directed by the Integrated Clinical Trial Team (iCT...
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useracceptancetesting lifesciences useracceptance systemintegration functionalsupport acceptancetesting clinicaldevelopment regulatorycompliance email oracle testing folders clinical compliance regulatory integration pharmacovigilance ISEPerform QC checks of draft protocol, draft CRF, draft ICF and other study related requirements. Observing the pre-check-in, check-in, pre-dose, dosing, post-dose activity as per protocol, SOP/IOPs re...
validationreports equipment tmf ria baggagehandlingsystems crf visit clinical clinicaldevelopment labels regulatoryguidelines qc checks protocol cfPerform QC checks of draft protocol, draft CRF, draft ICF and other study related requirements. Observing the pre-check-in, check-in, pre-dose, dosing, post-dose activity as per protocol, SOP/IOPs re...
validationreports equipment tmf ria baggagehandlingsystems crf visit clinical clinicaldevelopment labels regulatoryguidelines qc checks protocol cfPerform QC checks of draft protocol, draft CRF, draft ICF and other study related requirements. Observing the pre-check-in, check-in, pre-dose, dosing, post-dose activity as per protocol, SOP/IOPs re...
validation calibration monitoring regulatory protocol regulatoryguidelines completion validationreports pharmacology clinicaldevelopment nicalAbout 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 soYour responsibilities include, but are not limited to: Provides expert safety input to the clinical development program for assigned projects/products and be an active member of the Global Program Te...
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278199BR
Associate QC SpecialistJob Description
Your responsibilities include, but are not limited to:
1.Responsible for providing source data verification and ...
276979BR
Narrative WriterJob Description
Your responsibilities include, but are not limited to:
1. Independently write and QC/review patient narratives.
Medical Officers, often know as Chief Medical Officers, are physicians who are typically in charge at hospitals. Medical Officers serve as advisors on health issues and disease control, provide medica...
medical control medicine clinical nursing recruiting trials insurance opd surgery lectronicdatacapture diseasecontrol clinicaldevelopment goodclinicalpractice clinicalmonitoring clinicaltrialmanagementsystem cromanagement clinicaltrialsMedical Officers, often know as Chief Medical Officers, are physicians who are typically in charge at hospitals. Medical Officers serve as advisors on health issues and disease control, provide medica...
medical control medicine clinical nursing recruiting trials insurance opd surgery lectronicdatacapture diseasecontrol clinicaldevelopment goodclinicalpractice clinicalmonitoring clinicaltrialmanagementsystem cromanagement clinicaltrialsMedical Officers, often know as Chief Medical Officers, are physicians who are typically in charge at hospitals. Medical Officers serve as advisors on health issues and disease control, provide medica...
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278199BR
Associate QC SpecialistJob Description
Your responsibilities include, but are not limited to:
1.Responsible for providing source data verification and ...
Clinical research associate Job Description 1. Act as monitor of specific sites on a clinical study, under supervision, as appropriate. 2. Facilitate preparation and collection of site level documen...
documentation qa dra cra linicalresearch studymonitoring clinicaldevelopment queryresolution constructionplanning computerliteracy clinicalstudy clinicaltrialsJob Title: Regulatory Affairs (Biologics) Company: Leading BioPharma Company in Bangalore Location (USFDA Approved) Designation: Associate Director Reporting to: Head of Regulatory ...
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276979BR
Narrative WriterJob Description
Your responsibilities include, but are not limited to:
1. Independently write and QC/review patient narratives.
1] Head - Medical affairs (MA):
1] Head - Medical affairs (MA):
1] Head - Medical affairs (MA):
1] Head - Medical affairs (MA):
1] Head - Medical affairs (MA):
1] Head - Medical affairs (MA):
1] Head - Medical affairs (MA):
1] Head - Medical affairs (MA):
For 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 luste272652BR Clinical Research Associate Job Description Perform assigned activities to support monitoring of investigator sites and trial execution within the CPO under the supervision of Manager Clin...
basicdradocumentationcaregcphousecraichsupplysitelinicalresearchclinicaltrialsclinicaldevelopmentclinicalstudyconstructionplanningqueryresolutioncomputerliteracystudymonitoringClinical Research Associate Job Description 1. Act as monitor of specific sites on a clinical study, under supervision, as appropriate. 2. Facilitate preparation and collection of site level documen...
cradocumentationdraichgcplinicalresearchstudymonitoringclinicaldevelopmentqueryresolutionconstructionplanningcomputerliteracyclinicalstudyclinicaltrials273733BR 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...
riskmanagementplanshealthcareprofessionalsmedicalreviewpatientsafetyriskmanagementdatamanagementmedicalaffairsdrugdevelopmentclinicaldevelopmentdataregulatyaffairsregulatyrequirementsClinical research associate Job Description 1. Act as monitor of specific sites on a clinical study, under supervision, as appropriate. 2. Facilitate preparation and collection of site level documen...
documentationdracralinicalresearchstudymonitoringclinicaldevelopmentqueryresolutionconstructionplanningcomputerliteracyclinicalstudyclinicaltrialsClinical Research Associate Job Description 1. Act as monitor of specific sites on a clinical study, under supervision, as appropriate. 2. Facilitate preparation and collection of site level documen...
cragcpdradocumentationlinicaltrialsclinicalresearchclinicalstudystudymonitoringcomputerliteracyqueryresolutionconstructionplanningclinicaldevelopment269949BR Lead Medical Advisor Job Description Drives Novartis Brand adoption through provision of key medical knowledge of the brand. Provide thorough up- to- date medical, clinical development and...
strategyriskresearchadvisorymarketingsalesedicomarketingpharmabrandmarketingresearchpharmaceuticalmedicinesharedservicesclinicaldevelopmentWe are looking for candidates having experience of minimum 1 year in Pharmaceutical Industry handling Diabetic Segment. Candidates job will be totally field work. Candidates looking for change for b...
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