Remote ICH Guidelines Jobs
Remote from:
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
Sort by:
Sr. Medical Director, Drug Safety & Pharmacovigilance
Sr. Medical Director, Drug Safety & Pharmacovigilance
5 day ago
BridgeBio
- Remote: United States
- Full time
Risk ManagementSafety Instrumented SystemsDrug AdministrationPharmacovigilanceRegulatory ComplianceMedical Writing
Senior Clinical Research Associate - Northern England - FSP
Senior Clinical Research Associate - Northern England - FSP
11 day ago
Parexel
- Remote: United Kingdom
- Full time
HematologyClinical MonitoringOncologyICH GuidelinesgRPCClinical Trials
Senior Project Manager (US)
Senior Project Manager (US)
18 day ago
Innovaderm Research Inc.
- Remote: Maine (USA)
- Full time
Risk ManagementVendor ManagementProject ManagementBudget ManagementEducational PlanninggRPC
Clinical Operations Lead
Clinical Operations Lead
30+ days ago
Alimentiv
- Remote: Romania
- Full time
- Senior (5-10 years)
Oracle CRMgRPCICH GuidelinesProject ManagementVendor ManagementTask Management
Regulatory Affairs - Publishing
Regulatory Affairs - Publishing
26 day ago
Parexel
- Remote: Brazil
- Full time
ICH GuidelinesRegulatory ComplianceDigital File ManagementDigital MediaPerformance ImprovementClient Services
Medical Physician Specialist I
Medical Physician Specialist I
30+ days ago
Fortrea
- Remote: India
- Full time
- Junior (1-2 years)
- 38 - 38K
Adverse Event MonitoringRegulatory ComplianceCase AssessmentMedical DiagnosisMedical ScienceTherapeutic Modalities
Associé Bilingue de la Pharmacovigilance, Bilingue- Opportunité Future /Bilingual Drug Safety Associate- Future Opportunity
Associé Bilingue de la Pharmacovigilance, Bilingue- Opportunité Future /Bilingual Drug Safety Associate- Future Opportunity
30+ days ago
SmartSource
- Remote: Canada
- Full time
- Mid-level (2-5 years)
Clinical ResearchPharmacovigilanceData EntryQuality AssessmentFDA RegulationsICH Guidelines
Director Clinical Development, Solid Tumors
Director Clinical Development, Solid Tumors
6 day ago
BeiGene
- Remote: United States
- Full time
OncologyClinical Study DesignPre-Clinical DevelopmentClinical Trial Management SystemsRegulatory ComplianceClinical Data Management
CRA I/II临床监察员-肿瘤
CRA I/II临床监察员-肿瘤
30+ days ago
赛纽仕医药咨询(上海)有限公司
- Remote: China
- Full time
Web AdministrationRegulatory ComplianceClinical MonitoringInformed ConsentICH GuidelinesData Integrity
Senior Clinical Research Associate
Senior Clinical Research Associate
11 day ago
Parexel
- Remote: United Kingdom
- Full time
HematologyClinical MonitoringOncologyICH GuidelinesFDA RegulationsBuilding Inspections
Clinical Payments Specialist - Georgia/Brazil - Home-based
Clinical Payments Specialist - Georgia/Brazil - Home-based
30+ days ago
Worldwide Clinical Trials
- Remote: Brazil
- Full time
AnalyticsRegulatory ComplianceBudget ManagementCash ManagementData EntryData Validation
CRA II/Senior CRA
CRA II/Senior CRA
12 day ago
ICON plc
- Remote: Georgia (country)
- Full time
Clinical Trial PlanningICH GuidelinesPatient SafetyData IntegrityProtocol Implementation Conformance StatementClinical Research
M&S-QC Physico Chemistry Technician-Hangzhou
M&S-QC Physico Chemistry Technician-Hangzhou
30+ days ago
Sanofi
- Remote: China
- Full time
Analytical ChemistryAnalytical ProceduresEquipment Specification DevelopmentLaboratory EquipmentEquipment Specification DevelopmentStability Testing
Exec Dir, Project Delivery
Exec Dir, Project Delivery
19 day ago
Syneos Health
- Remote: California (USA)
- Full time
FDA RegulationsClinical ResearchProject ManagementCustomer Relationship ManagementICH GuidelinesRisk Management
Medical Director, Global Clinical Development, Inborn Errors of Metabolism
Medical Director, Global Clinical Development, Inborn Errors of Metabolism
2 day ago
Ultragenyx
- Remote: United States
- Full time
Regulatory ComplianceClinical MonitoringClinical Study DesignPre-Clinical DevelopmentHepatologyGastroenterology
Clinical Trial Associate, Clinical Operations
Clinical Trial Associate, Clinical Operations
30+ days ago
Lifelancer
- Remote: United States
- Full time
- Mid-level (2-5 years)
- 65 - 75K
Clinical Trial Management SystemsClinical ResearchGood Clinical Practices (GCP)ICH GuidelinesFDA Regulations
Associate Director, R&D Quality Systems
Associate Director, R&D Quality Systems
30+ days ago
Lifelancer
- Remote: United Kingdom
- Full time
- Senior (5-10 years)
Production PlanningGood Clinical Practices (GCP)PharmacovigilanceProject ManagementFDA RegulationsICH Guidelines
PV specialist
PV specialist
30+ days ago
Luminary Group
- Remote: United Kingdom
PharmacovigilanceAdverse Event MonitoringRegulatory CompliancePharmacovigilanceRisk ManagementSignal Handling
Medical Coding Specialist II
Medical Coding Specialist II
30+ days ago
Lifelancer
- Remote: United Kingdom
- Full time
- Mid-level (2-5 years)
Medical CodingMedDRAgRPCData ManagementWHO Drug Dictionary (WHO-DD)ICH Guidelines
Senior Data Manager
Senior Data Manager
30+ days ago
Alira Health
- Remote: Italy
- Full time
- Senior (5-10 years)
OncologySAS (Software)Medidata RaveData ManagementData CollectionData Validation
Director Clinical Development, Solid Tumors
Director Clinical Development, Solid Tumors
8 day ago
BeiGene
- Remote: United States
- Full time
OncologyClinical Study DesignPre-Clinical DevelopmentClinical TrialsRegulatory ComplianceClinical Data Management
Principal/Sr Medical Writer
Principal/Sr Medical Writer
30+ days ago
Lifelancer
- Remote: United Kingdom
- Full time
- Senior (5-10 years)
Statistical AnalysisClinical ResearchMedical WritingICH GuidelinesFDA RegulationsPresentation Training
Associate Director, Biostatistics
Associate Director, Biostatistics
30+ days ago
Lifelancer
- Remote: United States, New York (USA)
- Full time
- Senior (5-10 years)
- 185 - 235K
R (Programming Language)SAS (Software)BiostatisticsStatisticsStatistical AnalysisClinical Trials
Associate Director, Clinical Quality
Associate Director, Clinical Quality
2 day ago
Revolution Medicines
- Remote: United States
- Full time
Regulatory ComplianceAuditingRisk ManagementCritical AppraisalDOT (Department Of Transportation) InspectionsProcess Analysis
Sr. Medical Director
Sr. Medical Director
30+ days ago
Pacira BioSciences, Inc.
- Remote: United States
- Full time
- Mid-level (2-5 years)
- 3 - 3K
Best ExecutionClinical DocumentationPhysician CredentialingClinical ResearchDrug DevelopmentICH Guidelines
Senior Clinical Research Associate - Oncology Experience Required - UK (North/Midlands) - FSP
Senior Clinical Research Associate - Oncology Experience Required - UK (North/Midlands) - FSP
30+ days ago
Parexel
- Remote: United Kingdom
- Full time
Clinical Trial PlanningWeb AdministrationOncologyContinuous MonitoringICH GuidelinesClinical Research
Project Manager, Laboratory Services - Level Dependent on Experience
Project Manager, Laboratory Services - Level Dependent on Experience
30+ days ago
CTI Clinical Trial and Consulting Services
- Remote: United States, Kentucky (USA), Ohio (USA)
- 36 - 182K
Clinical Trial Management SystemsProject ManagementBudget ManagementLaboratory Information Management SystemsClinical Research CoordinationDrug Development
Clinical Scientist
Clinical Scientist
30+ days ago
Crinetics Pharmaceuticals
- Remote: California (USA)
- Full time
AnalyticsClinical ResearchRegulatory ComplianceClinical MonitoringGood Clinical Practices (GCP)ICH Guidelines
Clinical Research Associate II
Clinical Research Associate II
30+ days ago
Caidya
- Remote: United Kingdom
- Entry-level / graduate
Documentation GenerationICH GuidelinesWebsite MonitoringRegulatory ComplianceAdverse Event MonitoringProject Management
Senior Specialist, GMP Quality Assurance
Senior Specialist, GMP Quality Assurance
30+ days ago
Crinetics Pharmaceuticals
- Remote: United States, Canada, California (USA)
- Full time
- Senior (5-10 years)
- 83 - 110K
ICH GuidelinesProject CollaborationFDA RegulationsDosage FormMicrobiological TestingERP Systems Knowledge
Clinical Data Manager II (India)
Clinical Data Manager II (India)
30+ days ago
Lifelancer
- Remote: India
- Full time
- Expert & Leadership (>10 years)
Clinical Data ManagementClinical Database DevelopmentgRPCMedDRAWHO Drug Dictionary (WHO-DD)ICH Guidelines
Sr. Principal Scientist, Bioanalytical
Sr. Principal Scientist, Bioanalytical
30+ days ago
Glaukos Corporation
- Remote: California (USA)
- Full time
Pharmacokinetic DosingBiochemical TechniquesAbsorption Distribution Metabolism And Excretion (ADME)FDA RegulationsRegulatory ComplianceICH Guidelines
Pharmacovigilance Associate
Pharmacovigilance Associate
30+ days ago
SmartSource
- Remote: Canada
- Full time
- Junior (1-2 years)
Adverse Event MonitoringPharmacovigilanceClinical AssessmentsMedical AbbreviationsGood Documentation PracticesPresentation Training
Senior Data Manager
Senior Data Manager
30+ days ago
Alira Health
- Remote: Spain, United Kingdom, Germany, France, Italy
- Full time
- Mid-level (2-5 years)
ReconciliationDatabase ManagementData IntegrationUser Acceptance Testing (UAT)SAS (Software)MedDRA
Sr. Director/Executive Director, Analytical Development
Sr. Director/Executive Director, Analytical Development
3 day ago
BridgeBio
- Remote: United States
- Full time
Analytical ProceduresRegulatory ComplianceUV MappingRegulatory CompliancegRPCIRIX
senior Medical Director, Medical Affairs - Hematology - Europe - Remote
senior Medical Director, Medical Affairs - Hematology - Europe - Remote
30+ days ago
Lifelancer
- Remote: United Kingdom
- Full time
- Mid-level (2-5 years)
Medical JurisprudenceICH GuidelinesClinical ResearchFDA RegulationsTechnical TrainingHospital Experience
Senior Clinical Research Associate - West Coast
Senior Clinical Research Associate - West Coast
30+ days ago
BeiGene
- Remote: United States
- Full time
- Senior (5-10 years)
- 105 - 140K
General SurgeryClinical MonitoringApplication MonitoringICH GuidelinesDocumentation GenerationData Management
Manager, Clinical Operations Excellence
Manager, Clinical Operations Excellence
30+ days ago
Lifelancer
- Remote: United States, United Kingdom, Massachusetts (USA)
- Full time
- Senior (5-10 years)
- 112 - 140K
Process ImprovementGood Clinical Practices (GCP)Corrective And Preventive Action (CAPA)Clinical Trial Management SystemsICH GuidelinesPharmacy Experience
Clinical and Nonclinical Regulatory Writer (US or Canada)
Clinical and Nonclinical Regulatory Writer (US or Canada)
30+ days ago
Lifelancer
- Remote: United States, Minnesota (USA), North Carolina (USA)
- Full time
- Mid-level (2-5 years)
ICH GuidelinesFDA RegulationsPre-Clinical DevelopmentClinical DocumentationTechnical WritingProduct Knowledge
Sr Medical Writer (Clinical and Device Experience)
Sr Medical Writer (Clinical and Device Experience)
13 day ago
Syneos Health
- Remote: United States
- Full time
Clinical ResearchMedical WritingRegulatory ComplianceDigital File ManagementStatistical AnalysisPresentation Training
Manager, Study Start-up & Site Contracts
Manager, Study Start-up & Site Contracts
30+ days ago
MENARINI Group
- Remote: United States
- Full time
- Mid-level (2-5 years)
- 1 - 1K
Regulatory ComplianceClinical Trial Management SystemsContract ManagementICH GuidelinesContract Management
Director, CMC Biologics
Director, CMC Biologics
30+ days ago
Mirador Therapeutics
- Remote: United States, California (USA)
- Expert & Leadership (>10 years)
- 185 - 225K
Technological ChangeAssay DevelopmentManufacturing EngineeringProject ManagementICH GuidelinesFDA Regulations
Study Start-Up Country Specialist II
Study Start-Up Country Specialist II
30+ days ago
Caidya
- Remote: United States
- Full time
- Mid-level (2-5 years)
ICH GuidelinesGood Clinical Practices (GCP)Matrix ManagementMedical AbbreviationsMotivational LeadershipDigital File Management
Director, Clinical Development, Solid Tumor
Director, Clinical Development, Solid Tumor
30+ days ago
BeiGene
- Remote: United States
- Full time
- Senior (5-10 years)
- 232 - 292K
Clinical Trial Management SystemsOncologyPre-Clinical DevelopmentClinical Study DesignDrug DevelopmentICH Guidelines
Clinical Research Associate - Oncology - Michigan
Clinical Research Associate - Oncology - Michigan
30+ days ago
Lifelancer
- Remote: United States, New York (USA)
- Full time
- Mid-level (2-5 years)
Good Clinical Practices (GCP)Corporate Travel ManagementClinical ResearchProject CollaborationRecruitment StrategiesDatabase Management
Clinical Trial Manager II (CTM II)
Clinical Trial Manager II (CTM II)
30+ days ago
Caidya
- Remote: United States
- Full time
- Mid-level (2-5 years)
Recreational TherapyDocumentation GenerationICH GuidelinesClinical ResearchEstablishment LicensingClinical Trial Management Systems
Clinical Scientist, Associate Director/Director, Breast Cancer
Clinical Scientist, Associate Director/Director, Breast Cancer
30+ days ago
MENARINI Group
- Remote: United States
- Full time
- Senior (5-10 years)
- 175 - 230K
Drug DevelopmentClinical Study DesignPharmacovigilancegRPCBiostatisticsICH Guidelines
Senior Manager, GMP Vendor Quality
Senior Manager, GMP Vendor Quality
30+ days ago
Crinetics Pharmaceuticals
- Remote: United States, Canada, California (USA)
- Full time
- Senior (5-10 years)
- 114 - 152K
Risk ManagementSubstance DependenceContinuous Improvement ProcessProject ManagementFDA RegulationsVendor Management
Director, LATAM Clinical Operations
Director, LATAM Clinical Operations
30+ days ago
Alimentiv
- Remote: Latin America, Spain
- Full time
- Expert & Leadership (>10 years)
Clinical Trial Management SystemsRegulatory ComplianceProject ManagementClinical ResearchgRPCPerformance Metric
QA Manager, External Quality Vaccines - Asia
QA Manager, External Quality Vaccines - Asia
30+ days ago
Biolife Plasma Service
- Remote: United States
- Full time
- Senior (5-10 years)
Regulatory ComplianceHealth Risk AssessmentsTechnological ChangeChange ManagementDocument Development Life Cycle (DDLC)Validation Controls
