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1] Head - Medical affairs (MA):
" Q2 Solutions is a leading clinical trial laboratory services organization with end-to-end laboratory services and secure, enterprise-wide biospecimen and consent management solutions. With a relent...
clinicaltrials clinicaltrial lab trials medical science clinical management innovation milestones diagnostics ClinicalTrialManagementSystem yservices272510BR Statistical Programmer Job Description Your responsibilities: Your responsibilities include, but are not limited to: 1. Provide input as required at all meetings, discussions and activit...
sassasprogrammingsdtmdatamanagementphaseiclinicaltrialscomputerscienceinterpersonalskillsclinicaltrialtrialstingstatementsofwksowstatisticalreptingsummarizinginfmationSenior Scientific Writer I Job Description 1. Prepares manuscripts, literature review, abstracts, posters, and slide sets working from various data sources including clinical study reports, patient ...
sopagileadvisorycompliancemedicaltudyreportsclinicaltrialclinicalresearchcommunicationskillsproofreadingcustomermanagementprojectmanagementqualitycontrolclinicalstudycopyeditingScientific Writer 2 Job Description 1. Prepares literature review, abstracts, posters, and slide sets working from various data sources including clinical study reports, patient profiles etc. 2. Per...
sopagileadvisorycompliancemedicalprooftudyreportsclinicaltrialclinicalresearchcommunicationskillsproofreadingprojectmanagementqualitycontrolclinicalstudycopyeditingExpert Scientific Writer Job Description 1. Prepares literature review, abstracts, posters, and slide sets, Manuscripts (complex) working from various data sources including clinical study reports, ...
complianceagileadvisoryrocessimprovementqualitycontrolclinicalresearchprojectmanagementcopyeditingclinicaltrialclinicalstudystudyreportsproofreadingcustomermanagementcommunicationskills274292BR Manager - Regulatory Affairs Job Description To ensure product (Drug / Device) registration with the Drug Regulatory Agencies and maintenance of the license to operate . Responsibility in...
continuousimprovementfacilitationglobalteamsdrugtestinglifesciencesclinicaltrialsclinicaltrialnocpsurimpegulatyaffairsinfmationsystemregulatyagenciesregulatyrequirementsexpRecruitment,coordination & follow up of trial subjects, covering informed consent, adhering to safety and compliance issues sample collection & shipment Administer study drug Coordination & management...
clinicalresearchsitedocumentationsafetymedconsentclinicaltrialRecruitment,coordination & follow up of trial subjects, covering informed consent, adhering to safety and compliance issues sample collection & shipment Administer study drug Coordination & management...
clinicalresearchsitedocumentationsafetymedconsentclinicaltrialRecruitment,coordination & follow up of trial subjects, covering informed consent, adhering to safety and compliance issues sample collection & shipment Administer study drug Coordination & management...
clinicalresearchsitedocumentationsafetymedconsentclinicaltrialAct as the core project team lead to coordinate and manage all statistical programming activities Serve as the lead programmer to design and specify the overall approach to a project s programming ta...
sassasprogrammingsdtmdatamanagementstatisticalanalysisinterpersonalskillsstatisticalprogrammingclinicaltrialdesignoutputgraphsanalysisclinicaltingateliaisonregulatyguidelinesinfJob Description Global Pharmacovigilance and Risk Management Pharmacovigilance Specialist/Sr. Specialist Description: The Pharmacovigilance (PV) Specialist/Sr. Specialist will be responsible for ...
pharmacovigilancesafetycasecompliancequalityassurancedrugsafetyadverseeventsdataprocessingcaseprocessingclinicaltrialriskmeddramedicalmetricsclarifyclinicalendinfvendJob Description Global Pharmacovigilance and Risk Management Pharmacovigilance Specialist/Sr. Specialist Description: The Pharmacovigilance (PV) Specialist/Sr. Specialist will be responsible for ...
pharmacovigilancesafetycasecompliancequalityassurancedrugsafetyadverseeventsdataprocessingcaseprocessingclinicaltrialriskmeddramedicalmetricsclarifyclinicalendinfvendStatistical Programming Thorough understanding of clinical trial processes, from data collection to analysis reporting Prior experience and ability to lead and manage programmers in successful and t...
sassasprogrammingsdtmdatamanagementdatacollectionmanagementskillsprojectmanagementcommunicationskillsprojectadministrationclinicaltrialadamenglishanalysisclinicaltingkeffectivelymanagStatistical Programming 5-12 yrs. (Min 3 years study lead experience) Thorough understanding of clinical trial processes, from data collection to analysis reporting Prior experience and ability to ...
sassasprogrammingsdtmdatamanagementdatacollectionmanagementskillsprojectmanagementcommunicationskillsprojectadministrationclinicaltrialcvsenglishanalysisclinicaltingkeffectivelymanage268421BR Senior Scientific Writer II Job Description Prepares , literature review , abstracts , posters , and slide sets , and Manuscripts (complex) working from various data sources including clin...
agilecomplianceadvisoryustomermanagementcopyeditingstudyreportsqualitycontrolcommunicationskillsproofreadingprojectmanagementclinicalstudyclinicaltrialsharedservicesstatementsofworksow255992BR 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...
sharedservicesclinicaltrialsissuemanagementdrugdevelopmentlobaldrugdevelopmenthealthcareprofessionalsmedicalreviewpatientsafetyresearchmanagementregulatyrequirementsclinicaltrialsignaldeteResponsibilties You will be working in working in analytics and consulting specifically in the Pharmaceutical and Life sciences industry in areas like Market Intelligence , Technology scouting , Comp...
customerrelationsbasisaccountsresearchlifesciencessciencedirectpatentresearchmarketintelligencetechnologyscoutingcompetitiveintelligenceclinicaltrialimsdashexcelmidasusptopubmedtingscieThe objective of this project is to develop an application which uses R and allows researchers to access/analyze data. The application needs to perform end to end Network Meta-Analysis (NMA). It requi...
clinicaltrialsstatisticalmodelingjavapythonjavascriptstatisticsommercialmodelsclinicaltrialplotplotsesttrialscontextclinicalbayesianmetaphreptingmetaanalysis
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