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
241 jobs
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Director, Pharmaceutical Quality Systems
Director, Pharmaceutical Quality Systems
Today
Telix Pharmaceuticals Limited
- Remote: Japan, Australia, Switzerland, Belgium
- Full time
Digital File ManagementRegulatory ComplianceContinuous Improvement ProcessData IntegrityAuditingICH Guidelines
Senior Manager, Case Management
Senior Manager, Case Management
Today
Otsuka Pharmaceutical Companies (U.S.)
- Remote: United States
- Full time
Oracle ArgusPharmacovigilanceRegulatory ComplianceStrategic Decision MakingVendor ManagementCase Management Systems
Site Activation Partner I - FSP
Site Activation Partner I - FSP
1 day ago
Parexel
- Remote: Argentina, Mexico
- Full time
Clinical Trial Management SystemsRegulatory ComplianceDigital File ManagementClinical Trial PlanningFDA RegulationsICH Guidelines
Medical Information & Pharmacovigilance Specialist Nordics
Medical Information & Pharmacovigilance Specialist Nordics
1 day ago
Biomapas
- Remote: Finland, Denmark, Iceland, Norway
- Full time
Accident ReportingPharmacovigilanceRegulatory ComplianceMedical Record ManagementComputer ScienceLife Sciences
Senior Clinical Research Associate
Senior Clinical Research Associate
2 day ago
Parexel
- Remote: United Kingdom
- Full time
HematologyClinical MonitoringOncologyICH GuidelinesFDA RegulationsBuilding Inspections
Senior Clinical Research Associate - Northern England - FSP
Senior Clinical Research Associate - Northern England - FSP
2 day ago
Parexel
- Remote: United Kingdom
- Full time
HematologyClinical MonitoringOncologyICH GuidelinesgRPCClinical Trials
Director, Clinical Operations
Director, Clinical Operations
3 day ago
Immunovant
- Remote: New York (USA)
- Full time
General SurgeryRegulatory ComplianceProject ManagementGood Clinical Practices (GCP)Trial PreparationBudget Management
Site Care Partner I (Lead CRA), Oncology Experience Required - France - FSP
Site Care Partner I (Lead CRA), Oncology Experience Required - France - FSP
3 day ago
Parexel
- Remote: France
- Full time
Web AdministrationRegulatory ComplianceOncologyICH GuidelinesRecruitment StrategiesData Management
Regulatory Affairs - Publishing
Regulatory Affairs - Publishing
6 day ago
Parexel
- Remote: Argentina
- Full time
ICH GuidelinesRegulatory ComplianceDigital File ManagementDigital MediaClient ServicesProject Management
Senior Clinical Research Associate - Northern England - FSP
Senior Clinical Research Associate - Northern England - FSP
2 day ago
Parexel
- Remote: United Kingdom
- Full time
HematologyClinical MonitoringOncologyICH GuidelinesgRPCClinical Trials
Senior Clinical Research Associate - Oncology - Spain - FSP
Senior Clinical Research Associate - Oncology - Spain - FSP
2 day ago
Parexel
- Remote: Spain
- Full time
Clinical Trial PlanningWeb AdministrationClinical TrialsICH GuidelinesPhases Of Clinical ResearchClinical Research
Contract Senior Clinical Research Associate
Contract Senior Clinical Research Associate
9 day ago
Caidya
- Remote: United Kingdom
- Full time
Clinical MonitoringICH GuidelinesInternal DocumentationMedical AbbreviationsRemote Administration
Senior Clinical Research Associate
Senior Clinical Research Associate
2 day ago
Parexel
- Remote: United Kingdom
- Full time
HematologyClinical MonitoringOncologyICH GuidelinesFDA RegulationsBuilding Inspections
Senior Clinical Research Associate - Oncology - Spain - FSP
Senior Clinical Research Associate - Oncology - Spain - FSP
2 day ago
Parexel
- Remote: Spain
- Full time
Clinical Trial PlanningWeb AdministrationClinical TrialsICH GuidelinesPhases Of Clinical ResearchClinical Research
Clinical Trial Coordinator - FSP Dedicated - UK
Clinical Trial Coordinator - FSP Dedicated - UK
9 day ago
Thermo Fisher Scientific
- Remote: United Kingdom
- Full time
Clinical Research CoordinationRegulatory ComplianceAnalyticsProject ManagementDigital File ManagementCustomer Centricity
Program Manager, Clinical Research Operations - Remote - Nationwide
Program Manager, Clinical Research Operations - Remote - Nationwide
10 day ago
Vituity
- Remote: California (USA)
- Full time
Clinical System OperationsProject ManagementData EntryDatabase ManagementContract ManagementElectronic Data Capture (EDC)
Medical Writing Lead, Director F/M
Medical Writing Lead, Director F/M
30+ days ago
Lifelancer
- Remote: United Kingdom
- Full time
- Senior (5-10 years)
- 13 - 13K
Good Clinical Practices (GCP)Medical WritingFDA RegulationsProject ManagementICH GuidelinesProcess Improvement
Executive Director Clinical Scientist
Executive Director Clinical Scientist
7 day ago
Kura Oncology, Inc.
- Remote: California (USA)
- Full time
Clinical Trial PlanningAnalyticsLanguage InterpretationDrug DevelopmentBiostatisticsRegulatory Compliance
Senior Project Manager (Spain)
Senior Project Manager (Spain)
9 day ago
Innovaderm Research Inc.
- Remote: Spain
- Full time
Project Cost ManagementVendor ManagementProject ManagementRisk ManagementData ManagementMedical Writing
Clinical Study Builder (Poland)
Clinical Study Builder (Poland)
30+ days ago
Innovaderm Research Inc.
- Remote: Poland
- Full time
- Mid-level (2-5 years)
Case Report FormsVeevaDatabase ProgrammingSystems IntegrationEnd-User Training And SupportMedidata Rave
Principal Medical Writer (Portugal/Spain/France/Belgium/Germany/Hungary
Principal Medical Writer (Portugal/Spain/France/Belgium/Germany/Hungary
30+ days ago
Syneos Health
- Remote: Hungary, Portugal, Spain, United Kingdom, Belgium, Germany, France
Clinical ResearchMedical WritingRegulatory ComplianceData PresentationICH GuidelinesFDA Regulations
Clinical Study Builder (India)
Clinical Study Builder (India)
30+ days ago
Innovaderm Research Inc.
- Remote: India
- Full time
- Mid-level (2-5 years)
Good Clinical Practices (GCP)VeevaEnd-User Training And SupportCase Report FormsMedidata RaveDatabase Programming
Clinical Operations Leader (LSAD) - Oncology Experience Required - UK - FSP
Clinical Operations Leader (LSAD) - Oncology Experience Required - UK - FSP
30+ days ago
Parexel
- Remote: United Kingdom
- Full time
- Mid-level (2-5 years)
OncologyClinical Trial Management SystemsBudget ManagementCross-Functional CollaborationClinical ResearchRegulatory Compliance
Senior Study Start-Up Lead (SSUL)
Senior Study Start-Up Lead (SSUL)
30+ days ago
Caidya
- Remote: United Kingdom
- Full time
- Mid-level (2-5 years)
Clinical TrialsICH GuidelinesFinancial ManagementRegulatory Compliance
Syneos FSP CRA (I/II)临床监查员
Syneos FSP CRA (I/II)临床监查员
30 day ago
赛纽仕医药咨询(上海)有限公司
- Remote: China
- Full time
Web AdministrationGood Clinical Practices (GCP)Clinical Data ManagementPatient SafetyPharmacovigilanceRegulatory Compliance
Senior Project Manager (Argentina)
Senior Project Manager (Argentina)
30+ days ago
Innovaderm Research Inc.
- Remote: Argentina
- Full time
- Expert & Leadership (>10 years)
- 13 - 13K
Project ManagementProject Cost ManagementRisk ManagementVendor ManagementData ManagementMedical Writing
Principal Biostatistical Programmer
Principal Biostatistical Programmer
30+ days ago
Premier Research
- Remote: India
- Full time
- Senior (5-10 years)
Clinical TrialsComputational BiologyData ManagementICH GuidelinesSAS (Software)SAS (Software)
Principal Medical Writer - Remote
Principal Medical Writer - Remote
30+ days ago
MMS
- Remote: United Kingdom
- Full time
- Senior (5-10 years)
Clinical DocumentationGood Clinical Practices (GCP)Project ManagementScientific ReasoningStatistical Hypothesis TestingCode Of Federal Regulations
Senior Medical Science Liaison (Sr. MSL) – South Central
Senior Medical Science Liaison (Sr. MSL) – South Central
16 day ago
Bristol Myers Squibb
- Remote: Texas (USA)
- Full time
Clinical ResearchCommunication SciencesNuclear MedicineMedical OncologyDisease SurveillanceAcademic Writing
Medical Science Liaison, Medical Affairs – Southwest
Medical Science Liaison, Medical Affairs – Southwest
30+ days ago
ADC Therapeutics
- Remote: Cameroon
- 36 - 36K
HematologyPre-Clinical DevelopmentOncologyMedical GuidelineKey Opinion Leader DevelopmentReaction Mechanism
CRA Nederland - single sponsor
CRA Nederland - single sponsor
30+ days ago
Syneos Health
- Remote: Netherlands
- Full time
- Entry-level / graduate
Good Clinical Practices (GCP)ICH GuidelinesOncology
Pharmacovigilance Associate
Pharmacovigilance Associate
Today
SmartSource
- Remote: Canada
- Full time
Adverse Event MonitoringClinical AssessmentsPharmacovigilanceMedical GuidelineMedical AbbreviationsPaintShop Pro
Senior Statistical Programmer
Senior Statistical Programmer
30+ days ago
IQVIA
- Remote: Poland, South Africa, United Kingdom, Ireland
- Full time
SAS (Software)Statistical PackagesGood Clinical Practices (GCP)Data ValidationStatistical AnalysisProgram Standards
Freelance CRA II - Serbia (6 month contract)
Freelance CRA II - Serbia (6 month contract)
30+ days ago
Syneos Health
- Remote: Serbia
- Freelance
- Mid-level (2-5 years)
Web AdministrationGood Clinical Practices (GCP)ICH GuidelinesClinical Data ManagementPharmacovigilanceRegulatory Compliance
Director, Clinical Monitoring
Director, Clinical Monitoring
30+ days ago
Crinetics Pharmaceuticals
- Remote: California (USA), Texas (USA)
- Full time
- Senior (5-10 years)
- 163 - 204K
Good Clinical Practices (GCP)ICH GuidelinesRisk AnalyticsBiotechnologyElectronic EngineeringPharmaceutical Sciences
Clinical Trial Specialist
Clinical Trial Specialist
10 day ago
Alnylam Pharmaceuticals
- Remote: Massachusetts (USA)
- Full time
ICH GuidelinesClinical Trial Management SystemsGood Clinical Practices (GCP)System MonitoringWeb AdministrationRegulatory Compliance
Clinical Operations Lead
Clinical Operations Lead
30+ days ago
Alimentiv
- Remote: Poland
- Full time
- Senior (5-10 years)
Oracle CRMgRPCICH GuidelinesClinical DocumentationProject ManagementVendor Management
Clinical Research Associate (all levels), FSP, home based, client dedicated
Clinical Research Associate (all levels), FSP, home based, client dedicated
30+ days ago
Syneos Health
- Remote: Germany
- Full time
- Entry-level / graduate
Internal DocumentationSpeech FluencyICH GuidelinesPhases Of Clinical ResearchClinical InformaticsWeb Administration
Associate Medical Writer
Associate Medical Writer
30+ days ago
PSI CRO AG
- Remote: Canada
- Full time
- Mid-level (2-5 years)
Clinical DocumentationTracking Systems (Geolocation)FDA RegulationsMedical WritingOutcome InterpretationICH Guidelines
Medical Monitor (Oncology experience)
Medical Monitor (Oncology experience)
30+ days ago
ERGOMED
- Remote: Canada
Clinical MonitoringOncologyClinical ResearchMedical ManagementProblem ManagementDrug Administration
CMC Quality – Qualified Person (Contractor)
CMC Quality – Qualified Person (Contractor)
30+ days ago
Lifelancer
- Remote: United Kingdom
- Freelance
- Senior (5-10 years)
Clinical TrialsPharmaceutical EngineeringFDA RegulationsUSP StandardsICH GuidelinesStrategic Positioning
CRA II/Senior CRA
CRA II/Senior CRA
3 day ago
ICON plc
- Remote: Georgia (country)
- Full time
Clinical Trial PlanningICH GuidelinesPatient SafetyData IntegrityProtocol Implementation Conformance StatementClinical Research
Medical Writer I (Min 1yr experience)
Medical Writer I (Min 1yr experience)
30+ days ago
Lifelancer
- Remote: India
- Full time
- Junior (1-2 years)
Speech FluencyFreelance WritingClinical ResearchFDA RegulationsMedical WritingPresentation Training
Site Care Partner - FSP
Site Care Partner - FSP
8 day ago
Parexel
- Remote: Netherlands
- Full time
Web AdministrationRegulatory CompliancePatient SafetyData ManagementGood Clinical Practices (GCP)Clinical Trials
Director of Clinical Operations (global)
Director of Clinical Operations (global)
30+ days ago
OPIS
- Remote: Italy
- Full time
- Expert & Leadership (>10 years)
Clinical Trial Management SystemsBudget ManagementStakeholder CommunicationsRisk ManagementResource AllocationProject Management
FSP Ancillary Supplies CTC(Beijing)
FSP Ancillary Supplies CTC(Beijing)
25 day ago
Fortrea
- Remote: China
- Full time
Clinical Trial PlanningRegulatory ComplianceDigital File ManagementRegulatory ComplianceIEC 61508 StandardQuality Assessment
Clinical Study Builder (Contract - 1 year) / Concepteur d'Études Cliniques ( Contrat - 1 an)
Clinical Study Builder (Contract - 1 year) / Concepteur d'Études Cliniques ( Contrat - 1 an)
30+ days ago
Innovaderm Research Inc.
- Remote: Canada
- Fixed term
- Mid-level (2-5 years)
Database ProgrammingVeevaMedidata RaveData Quality AssessmentGood Clinical Practices (GCP)End-User Training And Support
Senior Statistical Programmer (m/w/d)
Senior Statistical Programmer (m/w/d)
7 day ago
IQVIA Italia
- Remote: Kenya, Estonia, Finland, Hungary, Poland, Romania, South Africa, United Kingdom, Sweden, Germany, Ireland, Serbia
- Full time
SAS (Software)Statistical PackagesGood Clinical Practices (GCP)Data ValidationStatistical AnalysisProgram Standards
Associate Manager, PSS
Associate Manager, PSS
30+ days ago
Lifelancer
- Remote: India
- Full time
- Senior (5-10 years)
- 38 - 38K
PharmacovigilanceProject ManagementRegulatory CompliancePatient SafetyPerformance ReviewData Entry
(Senior) Clinical Research Associate (New Zealand Wide & home-based)
(Senior) Clinical Research Associate (New Zealand Wide & home-based)
30+ days ago
BeiGene
- Remote: New Zealand
- Full time
- Mid-level (2-5 years)
Clinical MonitoringOncologygRPCICH GuidelinesData CollectionRegulatory Compliance
