Remote ICH Guidelines Jobs
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Software Development 17838B2B Sales & Account Management 10968CRM & Direct Marketing 10917Product 9303Back-End Development 9223Management and Leadership 8423Data and Analytics 8147finance 8094IT & Engineering 6553Enterprise Sales 6500Project & Program Management 5958Customer Support & Service 5958Sustainability & CSR 5474Sales Leadership & Strategy 5011DevOps & Infrastructure 4737Growth & Performance 3338Front-End Development 2857
223 jobs
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Sr Medical Writer (Medical Device)
Sr Medical Writer (Medical Device)
30+ days ago
Lifelancer
- Remote: United Kingdom
- Full time
- Senior (5-10 years)
- 60 - 115K
Clinical ResearchMedical WritingICH GuidelinesFDA RegulationsPresentation TrainingDigital File Management
Clinical Trial Specialist
Clinical Trial Specialist
19 day ago
Alnylam Pharmaceuticals
- Remote: Massachusetts (USA)
- Full time
ICH GuidelinesClinical Trial Management SystemsGood Clinical Practices (GCP)System MonitoringWeb AdministrationRegulatory Compliance
Director, Pharmaceutical Quality Systems
Director, Pharmaceutical Quality Systems
9 day ago
Telix Pharmaceuticals Limited
- Remote: Japan, Australia, Switzerland, Belgium
- Full time
Digital File ManagementRegulatory ComplianceContinuous Improvement ProcessData IntegrityAuditingICH Guidelines
Senior Project Manager / Gestionnaire de projets (Canada)
Senior Project Manager / Gestionnaire de projets (Canada)
30+ days ago
Innovaderm Research Inc.
- Remote: Canada
- Full time
- Expert & Leadership (>10 years)
- 13 - 28K
Clinical Trial Management SystemsProject ManagementBudget ManagementBusiness CommunicationRisk ManagementgRPC
Site Start-up Specialist
Site Start-up Specialist
30+ days ago
Fortrea
- Remote: Estonia, Republic of Lithuania
- Full time
ICH GuidelinesClinical ResearchRegulatory ComplianceDigital File ManagementRegulatory ComplianceInformed Consent
Senior Auditor, Clinical Quality and Compliance, Poland
Senior Auditor, Clinical Quality and Compliance, Poland
30+ days ago
Innovaderm Research Inc.
- Remote: Poland
- Full time
- Senior (5-10 years)
Risk AnalysisClinical Quality ManagementHealth LawsFDA RegulationsICH GuidelinesLanguage Education
Sr Medical Writer - UK
Sr Medical Writer - UK
30+ days ago
Stemline Therapeutics
- Remote: United Kingdom
- Full time
- Expert & Leadership (>10 years)
Project CollaborationDrug DevelopmentICH GuidelinesPharmaceutical SciencesStatisticsMedical Writing
Site Care Partner - FSP
Site Care Partner - FSP
17 day ago
Parexel
- Remote: Netherlands
- Full time
Web AdministrationRegulatory CompliancePatient SafetyData ManagementGood Clinical Practices (GCP)Clinical Trials
Pharmacovigilance Associate
Pharmacovigilance Associate
9 day ago
SmartSource
- Remote: Canada
- Full time
Adverse Event MonitoringClinical AssessmentsPharmacovigilanceMedical GuidelineMedical AbbreviationsPaintShop Pro
Clinical Trial Associate
Clinical Trial Associate
30+ days ago
Lifelancer
- Remote: United Kingdom
- Full time
Clinical Trial Management SystemsProtocol AnalysisICH GuidelinesContinuous MonitoringTrial PreparationProject Management
Medical Writer II (Lay Summaries/Plain Language Summaries)
Medical Writer II (Lay Summaries/Plain Language Summaries)
11 day ago
Syneos Health
- Remote: Spain
- Full time
Clinical Study DesignRegulatory ComplianceDrug DevelopmentMedical WritingRegulatory ComplianceLanguage Education
Senior Medical Writer (Remote)
Senior Medical Writer (Remote)
30+ days ago
MMS
- Remote: United Kingdom
- Full time
- Mid-level (2-5 years)
Medical WritingCreative WritingPharmacy ExperienceGood Clinical Practices (GCP)ICH GuidelinesPip (Software)
Regional Clinical Trial Management (Senior) Associate
Regional Clinical Trial Management (Senior) Associate
30+ days ago
BeiGene
- Remote: Malaysia
- Full time
- Mid-level (2-5 years)
- 10 - 10K
ICH GuidelinesClinical ResearchBudget ManagementVendor ManagementProject ManagementBiotechnology
CRA II
CRA II
4 day ago
ICON plc
- Remote: Australia
- Full time
Clinical Data AnalysisICH GuidelinesClinical Trial Management SystemsFeasibility StudiesDocumentation GenerationStakeholder Communications
Sr Medical Writer (FSP)
Sr Medical Writer (FSP)
30+ days ago
Lifelancer
- Remote: United Kingdom
- Full time
- Senior (5-10 years)
Project ManagementClinical ResearchMedical WritingFDA RegulationsStatistical AnalysisPresentation Training
Senior Director, Clinical Operations
Senior Director, Clinical Operations
8 day ago
tactical.
- Remote: United Arab Emirates
- Full time
Clinical System OperationsProject ManagementCancer ImmunologyRegulatory ComplianceClinical MonitoringStatistical Analysis
Line Manager, Regulatory Documents Assistant
Line Manager, Regulatory Documents Assistant
30+ days ago
Innovaderm Research Inc.
- Remote: India
- Full time
Regulatory ComplianceClinical ResearchPerformance ManagementClinical Trial PlanningICH GuidelinesProcess Improvement
Senior Clinical Research Associate
Senior Clinical Research Associate
30+ days ago
BeiGene
- Remote: Poland
- Full time
- Mid-level (2-5 years)
ICH GuidelinesClinical MonitoringgRPCClinical TrialsSite AnalysisRegulatory Compliance
Director, GCP Process Excellence
Director, GCP Process Excellence
17 day ago
Takeda
- Remote: Massachusetts (USA)
- Full time
Clinical Trial PlanninggRPCStandard Operating ProcedureRegulatory ComplianceChange ManagementPharmaceutical Sciences
Site Activation Partner I - FSP
Site Activation Partner I - FSP
10 day ago
Parexel
- Remote: Argentina, Mexico
- Full time
Clinical Trial Management SystemsRegulatory ComplianceDigital File ManagementClinical Trial PlanningFDA RegulationsICH Guidelines
Contractual Clinical Research Associate (experience in Dermatology) - Slovakia
Contractual Clinical Research Associate (experience in Dermatology) - Slovakia
30 day ago
Innovaderm Research Inc.
- Remote: Slovakia
- Freelance
ICH GuidelinesClinical MonitoringDermatologyWebsite MonitoringData ValidationRegulatory Compliance
Senior Central Risk Manager (India)
Senior Central Risk Manager (India)
30+ days ago
Innovaderm Research Inc.
- Remote: India
- Full time
- Expert & Leadership (>10 years)
Clinical ResearchRisk ManagementRisk AnalyticsData QualityGood Clinical Practices (GCP)Data Visualization
Clinical Research Associate
Clinical Research Associate
30+ days ago
BeiGene
- Remote: Netherlands, Belgium
- Full time
Clinical MonitoringgRPCICH GuidelinesClinical TrialsRegulatory ComplianceWeb Administration
Clinical Study Builder (Germany)
Clinical Study Builder (Germany)
30+ days ago
Innovaderm Research Inc.
- Remote: Germany
- Full time
- Mid-level (2-5 years)
Medidata RaveVeevaCase Report FormsSystems IntegrationData Quality AssessmentEnd-User Training And Support
Associate Director, Biostatistics
Associate Director, Biostatistics
5 day ago
Genmab
- Remote: Netherlands
- Full time
Adaptive Clinical TrialsBiostatisticsStatistical ModelingStatistical AnalysisRegulatory ComplianceICH Guidelines
Medical Editor II (Early Phase - Canada Based)
Medical Editor II (Early Phase - Canada Based)
27 day ago
Syneos Health
- Remote: Canada
- Full time
Data IntegrityProject ManagementMedical WritingCopy EditingISO 13485 StandardICH Guidelines
Medical Information & Pharmacovigilance Specialist Nordics
Medical Information & Pharmacovigilance Specialist Nordics
10 day ago
Biomapas
- Remote: Finland, Denmark, Iceland, Norway
- Full time
Accident ReportingPharmacovigilanceRegulatory ComplianceMedical Record ManagementComputer ScienceLife Sciences
Quality Systems Specialist/ Spécialiste des Systèmes de Qualité
Quality Systems Specialist/ Spécialiste des Systèmes de Qualité
30+ days ago
Innovaderm Research Inc.
- Remote: Canada
- Full time
- Mid-level (2-5 years)
AuditingArtificial IntelligenceVendor ManagementClinical Quality ManagementICH GuidelinesCosmetic Dermatology
Principal Medical Writer
Principal Medical Writer
30+ days ago
Lifelancer
- Remote: United Kingdom
- Full time
Data PresentationClinical ResearchMedical WritingFDA RegulationsStatistical AnalysisICH Guidelines
Clinical Research Associate
Clinical Research Associate
30+ days ago
BeiGene
- Remote: France
- Full time
- Mid-level (2-5 years)
Clinical MonitoringMedical OncologygRPCICH GuidelinesData CollectionProject Management
Medical Writer, Non-Clinical H/F
Medical Writer, Non-Clinical H/F
30+ days ago
Lifelancer
- Remote: United Kingdom
- Full time
- Mid-level (2-5 years)
Pharmaceutical MarketingProject ManagementMedical WritingICH GuidelinesDrug DevelopmentPharmacology
Senior Project Manager (Poland)
Senior Project Manager (Poland)
18 day ago
Innovaderm Research Inc.
- Remote: Poland
- Full time
Project Cost ManagementVendor ManagementProject ManagementRisk ManagementData ManagementMedical Writing
Senior Medical Manager Skeletal Conditions Germany
Senior Medical Manager Skeletal Conditions Germany
15 day ago
BioMarin Pharmaceutical Inc.
- Remote: Germany
- Full time
Stakeholder CommunicationsHospital ExperienceScientific StudiesCross-Functional CollaborationBudget ManagementRegulatory Compliance
Local Study Associate Director - Remote - FSP
Local Study Associate Director - Remote - FSP
30+ days ago
Lifelancer
- Remote: United Kingdom
- Full time
- Mid-level (2-5 years)
ICH GuidelinesClinical ResearchClinical TrialsClinical Trial Management SystemsBudget ManagementRegulatory Compliance
Medical Editor II (Early Phase - Canada Based)
Medical Editor II (Early Phase - Canada Based)
24 day ago
Syneos Health
- Remote: Canada
- Full time
Data IntegrityProject ManagementMedical WritingCopy EditingISO 13485 StandardICH Guidelines
Clinical Payments Specialist - Turkish speaker - Home-based
Clinical Payments Specialist - Turkish speaker - Home-based
21 day ago
Worldwide Clinical Trials
- Remote: Czechia
- Full time
Project ManagementBudget ManagementData ValidationFDA RegulationsICH Guidelines
Experienced Study Start up Submissions Coordinator
Experienced Study Start up Submissions Coordinator
30+ days ago
Medpace
- Remote: India
- Mid-level (2-5 years)
Regulatory ComplianceRisk AnalysisICH GuidelinesRegulatory ComplianceClinical TrialsOrganizational Structure
Exec Dir, Project Delivery
Exec Dir, Project Delivery
24 day ago
Syneos Health
- Remote: Canada
- Full time
ICH GuidelinesFDA RegulationsClinical ResearchProject ManagementDrug DevelopmentClinical Monitoring
Local Study Manager
Local Study Manager
3 day ago
AstraZeneca
- Remote: United States
- Full time
Operational PlanningClinical Study DesignCell TherapyICH GuidelinesData IntegrationProject Management
Clinical Trial Specialist
Clinical Trial Specialist
19 day ago
Alnylam Pharmaceuticals
- Remote: Massachusetts (USA)
- Full time
ICH GuidelinesClinical Trial Management SystemsGood Clinical Practices (GCP)System MonitoringWeb AdministrationRegulatory Compliance
Clinical Data Management Systems Specialist Contractor (RAVE Admin) (Office OR Remote)
Clinical Data Management Systems Specialist Contractor (RAVE Admin) (Office OR Remote)
30+ days ago
Lifelancer
- Remote: United Kingdom
- Freelance
- Mid-level (2-5 years)
Clinical Data ManagementPrivileged Access ManagementCodesmithCBASICMedDRALaboratory Management System
Sr Medical Writer (Spain/Portugal/Poland and Romania)
Sr Medical Writer (Spain/Portugal/Poland and Romania)
30+ days ago
Lifelancer
- Remote: Portugal, Spain, United Kingdom
- Full time
- Senior (5-10 years)
Clinical ResearchMedical WritingFDA RegulationsStatistical AnalysisPresentation TrainingICH Guidelines
QA Manager, External Quality Vaccines - Asia
QA Manager, External Quality Vaccines - Asia
8 day ago
Takeda
- Remote: India
- Full time
Regulatory ComplianceChange ManagementLifecycle ManagementProject ManagementVerification And ValidationRisk Management
Associate Global Biometrics Delivery Lead - select EMEA locations
Associate Global Biometrics Delivery Lead - select EMEA locations
16 day ago
Parexel
- Remote: Poland, Romania, South Africa, United Kingdom
- Full time
Data ManagementStatistical ThinkingProject ManagementDatabase ProgrammingCross-Functional CollaborationHealth Data Standards
Principal Medical Writer
Principal Medical Writer
30+ days ago
Lifelancer
- Remote: United Kingdom
- Full time
- Senior (5-10 years)
Pre-Clinical DevelopmentMedical WritingProject ManagementOnline CommunicationICH GuidelinesPharmacy Experience
Experienced Study Start up Submissions Coordinator
Experienced Study Start up Submissions Coordinator
30+ days ago
Medpace
- Remote: India
- Mid-level (2-5 years)
Risk AnalysisICH GuidelinesOrganizational StructureRegulatory ComplianceRegulatory ComplianceRegulatory Compliance
Clinical Study Builder / Concepteur d'Études Cliniques
Clinical Study Builder / Concepteur d'Études Cliniques
30+ days ago
Innovaderm Research Inc.
- Remote: Canada
- Full time
- Mid-level (2-5 years)
Regulatory ComplianceVeevaData ManagementGood Clinical Practices (GCP)Medidata RaveDatabase Programming
Director, Internal and Contracted Audits Program - UK - Home-based
Director, Internal and Contracted Audits Program - UK - Home-based
30+ days ago
Worldwide Clinical Trials
- Remote: United Kingdom
- Full time
- Expert & Leadership (>10 years)
- 5 - 5K
ICH GuidelinesSocial InfluencesProcess ImprovementPresentation TrainingAuditingFDA Regulations
Syneos CRA(I/II)临床监查员
Syneos CRA(I/II)临床监查员
30+ days ago
赛纽仕医药咨询(上海)有限公司
- Remote: China
- Full time
Web AdministrationGood Clinical Practices (GCP)Data CollectionClinical MonitoringPharmacovigilanceProspect Meetings
Project Manager (Cold Form Structural Engineering)- Milwaukee, WI, (REMOTE)
Project Manager (Cold Form Structural Engineering)- Milwaukee, WI, (REMOTE)
30+ days ago
Futurerecruit.net
- Remote: Wisconsin (USA)
- Full time
Steel DesignEngineering EthicsICH GuidelinesRisa (Structural Engineering Software)
