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
235 jobs
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Associate Director, GCP Compliance
Associate Director, GCP Compliance
7 day ago
BioMarin Pharmaceutical Inc.
- Remote: United States
- Full time
Regulatory ComplianceAuditingGeneral SurgeryClinical Trial Management SystemsICH GuidelinesFDA Regulations
Senior Manager, Medical Writing
Senior Manager, Medical Writing
30+ days ago
BeiGene
- Remote: United States
- Full time
- Senior (5-10 years)
- 138 - 183K
Project ManagementMedical WritingFDA RegulationsBiostatisticsICH GuidelinesRegulatory Compliance
Director, Training and Knowledge Management
Director, Training and Knowledge Management
10 day ago
BeiGene
- Remote: United States
- Full time
Clinical System OperationsTrain The TrainerLearning Management SystemsDeveloping Training MaterialsPresentation TrainingICH Guidelines
Senior Medical Science Liaison (Sr. MSL) – Southwest
Senior Medical Science Liaison (Sr. MSL) – Southwest
24 day ago
Bristol Myers Squibb
- Remote: United States
- Full time
Communication SciencesNuclear MedicineMedical ScienceRegulatory ComplianceClinical ConsultingClinical Research
Clinical Research Associate
Clinical Research Associate
30+ days ago
Crinetics Pharmaceuticals
- Remote: United States, Canada, California (USA)
- Full time
- Entry-level / graduate
- 84 - 105K
Data ManagementClinical Trial Management SystemsGood Clinical Practices (GCP)Professional WritingRisk AnalyticsICH Guidelines
Lead, Clinical Operations
Lead, Clinical Operations
30+ days ago
Lifelancer
- Remote: United States, Massachusetts (USA)
- Full time
- Senior (5-10 years)
Clinical System OperationsProject ManagementRisk ManagementVendor ManagementDocumentation GenerationClinical Trial Planning
Principal Biostatistician
Principal Biostatistician
30+ days ago
Apellis Pharmaceuticals
- Remote: United States
- Full time
Statistical MethodsBiostatisticsSAS (Software)R (Programming Language)Regulatory ComplianceSample Size Determination
Associate Director, Programming
Associate Director, Programming
30+ days ago
Takeda
- Remote: United States, New Jersey (USA)
- Full time
- Expert & Leadership (>10 years)
- 149 - 234K
ICH GuidelinesProcess ImprovementMachine LearningFDA RegulationsTechnical LeadershipCross-Functional Collaboration
Senior Manager, Clinical Data Management (Oncology)
Senior Manager, Clinical Data Management (Oncology)
30+ days ago
Biolife Plasma Service
- Remote: United States, Massachusetts (USA)
- Full time
- Senior (5-10 years)
Project ManagementVendor ManagementClinical Data ManagementEcoSys (Project Management Software)Data Transfer ObjectData Validation
CRA II- Southeast Region- Oncology- Sponsor Dedicated
CRA II- Southeast Region- Oncology- Sponsor Dedicated
30+ days ago
Lifelancer
- Remote: United States, Alabama (USA)
- Full time
- Mid-level (2-5 years)
- 70 - 126K
Clinical MonitoringICH GuidelinesGood Clinical Practices (GCP)Continuous MonitoringInformed ConsentQuery Planning
Sr. Manager/AD, Biostatistics
Sr. Manager/AD, Biostatistics
30+ days ago
Immunovant
- Remote: United States
- Senior (5-10 years)
- 190 - 200K
Statistical MethodsStatistical AnalysisBiostatisticsRegulatory ComplianceClinical TrialsClinical Study Design
Vice President, Late-Stage Clinical Development (Remote)
Vice President, Late-Stage Clinical Development (Remote)
30+ days ago
Lifelancer
- Remote: United States, California (USA)
- Internships
- Senior (5-10 years)
- 354 - 447K
Clinical Study DesignOphthalmologyPre-Clinical DevelopmentGene TherapyClinical MonitoringPharmacovigilance
Sr Medical Writer (Oncology regulatory)
Sr Medical Writer (Oncology regulatory)
10 day ago
Syneos Health
- Remote: United States
- Full time
Regulatory ComplianceOncologyClinical ResearchMedical WritingStatistical AnalysisPresentation Training
REMS Project Manager
REMS Project Manager
28 day ago
UBC
- Remote: United States
- Full time
Regulatory ComplianceRisk ManagementProject ManagementBudget ManagementStakeholder CommunicationsClinical Trial Planning
TMF Specialist
TMF Specialist
30+ days ago
Crinetics Pharmaceuticals
- Remote: United States, Canada, California (USA)
- Full time
- Entry-level / graduate
- 68 - 90K
Clinical ResearchRegulatory ComplianceICH GuidelinesCBASICClinical DocumentationProject Management
Biostatistician II
Biostatistician II
30+ days ago
Precision Medicine Group
- Remote: United States
- Mid-level (2-5 years)
- 80 - 120K
Statistical AnalysisSAS (Software)Clinical TrialsStatistical ModelingStatistical MethodsStatistical Theory
Associate Director, Clinical Trial Operations
Associate Director, Clinical Trial Operations
18 day ago
Crinetics Pharmaceuticals
- Remote: United States
- Full time
Regulatory ComplianceClinical Trial Management SystemsProject ManagementRisk ManagementData ManagementBudget Management
Manager, QMS Record Management (Contractor)
Manager, QMS Record Management (Contractor)
30+ days ago
Lifelancer
- Remote: United States
- Freelance
- Senior (5-10 years)
Regulatory ComplianceProject ManagementCross-Functional CollaborationICH GuidelinesISO 20022Access Controls
Associate Medical Writer
Associate Medical Writer
30+ days ago
PSI CRO AG
- Remote: United States
- Full time
- Mid-level (2-5 years)
Clinical DocumentationFDA RegulationsMedical WritingOutcome InterpretationICH Guidelines
In-House Clinical Research Associate
In-House Clinical Research Associate
30+ days ago
Alira Health
- Remote: United States
- Junior (1-2 years)
ICH GuidelinesFDA RegulationsClinical Assessments
Senior Manager, Clinical Data Management (Oncology)
Senior Manager, Clinical Data Management (Oncology)
30+ days ago
Takeda
- Remote: United States, Massachusetts (USA)
- Senior (5-10 years)
Clinical Data ManagementVendor ManagementProject ManagementData ManagementDrug DevelopmentEcoSys (Project Management Software)
Sr. Manager, Data Management
Sr. Manager, Data Management
30+ days ago
Taiho Oncology, Inc.
- Remote: United States
- Full time
Data ManagementClinical Data ManagementMedical OncologyMedidata RaveData ValidationRegulatory Compliance
Clinical Research Associate II
Clinical Research Associate II
30+ days ago
Caidya
- Remote: United States
- Full time
Internal DocumentationMatrix ManagementContinuous MonitoringICH GuidelinesMedical Abbreviations
Sr. Clinical Studies Analyst (Pediatric Clinical Studies)
Sr. Clinical Studies Analyst (Pediatric Clinical Studies)
30+ days ago
Lifelancer
- Remote: United States, Illinois (USA), Pennsylvania (USA)
- Full time
- Expert & Leadership (>10 years)
Pre-Clinical DevelopmentProject ManagementTherapeutic ModalitiesVaccine DevelopmentRisk AnalysisClinical Trials
Clinical Research Associate II
Clinical Research Associate II
30+ days ago
Caidya
- Remote: United States
- Full time
- Entry-level / graduate
Website MonitoringRegulatory ComplianceICH GuidelinesInternal DocumentationHighway DrivingData Validation
Scientific Consultant - Statistics
Scientific Consultant - Statistics
30+ days ago
BryceTech
- Remote: United States, District of Columbia (USA)
- Full time
- Senior (5-10 years)
Meeting FacilitationTabular DataMilitary ServiceData IntegrationSAS (Software)ICH Guidelines
Sr. Manager, Data Management
Sr. Manager, Data Management
30+ days ago
Taiho Oncology, Inc.
- Remote: United States
- Full time
Data ManagementOncologyClinical Data ManagementMedidata RaveData ValidationProject Management
Sr. Oversight Clinical Research Associate
Sr. Oversight Clinical Research Associate
30+ days ago
Apogee Therapeutics
- Remote: United States
- Full time
Data IntegrityClinical ResearchWebsite MonitoringVendor ManagementGood Clinical Practices (GCP)Protocol Analysis
Clinical Study Builder (Spain)
Clinical Study Builder (Spain)
30+ days ago
Innovaderm Research Inc.
- Remote: United States, Spain, Maryland (USA)
- Full time
- Mid-level (2-5 years)
Medidata RaveVeevaDatabase ProgrammingCase Report FormsICH GuidelinesGood Clinical Practices (GCP)
Specialist I, Process & Quality, Project Delivery Office
Specialist I, Process & Quality, Project Delivery Office
17 day ago
Fortrea
- Remote: India
- Full time
Clinical ResearchChange ManagementProject ManagementQuality AssessmentDrug DevelopmentPharmaceutical Sciences
Clinical Team Lead
Clinical Team Lead
17 day ago
Fortrea
- Remote: Brazil
- Full time
Budget ManagementProject ManagementRisk ManagementMicrosoft AccessgRPCProject Management
Associate Director, Drug Safety & Pharmacovigilance Operations
Associate Director, Drug Safety & Pharmacovigilance Operations
17 day ago
Sage Therapeutics
- Remote: United States
- Full time
Regulatory ComplianceDrug AdministrationPharmacovigilanceCross-Functional CollaborationProcess ImprovementVendor Management
CRA II and Senior CRA
CRA II and Senior CRA
17 day ago
ICON plc
- Remote: Illinois (USA), Oregon (USA)
- Full time
Clinical Trial PlanningOncologyData IntegrityICH GuidelinesPatient SafetyDocumentation Generation
(Senior) Regulatory and Start Up Specialist 
(Senior) Regulatory and Start Up Specialist
18 day ago
PRECISIONeffect
- Remote: France
- Full time
Regulatory ComplianceBudget AnalysisContract ManagementBioethicsProject ManagementGood Clinical Practices (GCP)
(Senior) Regulatory and Start Up Specialist 
(Senior) Regulatory and Start Up Specialist
18 day ago
Precision For Medicine
- Remote: France
- Full time
Regulatory ComplianceBudget AnalysisContract ManagementGood Clinical Practices (GCP)Project ManagementBioethics
