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Remote Senior Clinical Research Specialist Jobs

Search 23 active remote senior clinical research specialist jobs. No recruiters, no spam - just real jobs from real companies.

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Ergomed

Senior Benefit/Risk Associate

🕒 7 days ago
Ergomed👥 501 - 1000 employees🏢 Biotechnology

Perform and support pharmacovigilance signal management, from reviewing safety data and evaluating potential signals to drafting reports and supporting regulatory communications.

PharmacovigilanceSignal DetectionSignal ManagementSignal Detection Reporting

Manage clinical trial sites and protocol compliance across study phases, conducting monitoring visits, supporting site performance and recruitment, and partnering with investigators and internal teams.

📍 🇺🇸 New Jersey Rahway - Remote💰 $129k - $203.1k / year💼 Full-Time🎸 Senior🎲 Other📢 🇬🇧 English Required📢 🇪🇸 Spanish Required
Clinical ResearchClinical Trial MonitoringSite ManagementICH/GCP Compliance

Conducts clinical trial monitoring across Spain and Portugal, assessing investigator and site readiness, training site staff, and supporting regulatory submissions for Phase 2/3 studies.

📍 🇵🇹 Portugal - Remote💼 Full-Time🎸 Senior🧫 Clinical Research Specialist📢 🇪🇸 Spanish Required📢 🇧🇷🇵🇹 Portuguese Required
Clinical Trial MonitoringPhase 2/3 TrialsOncologyRare Disease

Conduct pre-study, initiation, interim, and close-out monitoring visits in Spain and Portugal, verifying site and investigator readiness, training staff, and supporting regulatory or ethics committee submissions.

📍 🇪🇸 Spain - Remote💼 Full-Time🎸 Senior🧫 Clinical Research Specialist📢 🇪🇸 Spanish Required📢 🇧🇷🇵🇹 Portuguese Required
Clinical Trial MonitoringPhase 2/3 TrialsOncologyRare Disease
Allucent

Sr Clinical Research Associate Contractor (Belarus)

🕒 10 days ago
Allucent👥 501 - 1000 employees🏢 Pharmaceuticals

Independently oversee clinical trial monitoring from site initiation through close-out, maintaining GCP and regulatory compliance, strong investigator relationships, data quality, and trial integrity.

Clinical Trial MonitoringClinical ResearchICH-GCPRegulatory Compliance
Ergomed

Senior Pharmacovigilance Associate

🕒 11 days ago
Ergomed👥 501 - 1000 employees🏢 Biotechnology

Manage individual case safety reports and related pharmacovigilance activities, ensuring regulatory and client-specific compliance while supporting patient safety, reporting, and local safety processes.

PharmacovigilanceIndividual Case Safety Report (icsr) ProcessingICSR Follow-upSAE/SUSAR Management
Ergomed

Clinical Research Associate II / Senior CRA (French Speaking)

🕒 14 days ago
Ergomed👥 501 - 1000 employees🏢 Biotechnology

Conducts clinical trial monitoring visits and supports investigational sites through study start-up, ongoing oversight, and close-out, helping maintain site readiness and study quality in complex trials.

📍 🇪🇸 Spain - Remote💼 Full-Time🎸 Senior🧫 Clinical Research Specialist📢 🇫🇷 French Required📢 🇬🇧 English Required
Clinical Trial MonitoringPhase 2/3 TrialsOncologyRare Disease
PSI CRO

Senior Clinical Research Associate

🕒 14 days ago
PSI CRO👥 1001 - 5000 employees🏢 Pharmaceuticals

Manage clinical trial activities across global studies, overseeing site monitoring, data quality, and stakeholder communication while mentoring junior CRAs and supporting investigators and study teams.

Clinical Trial MonitoringSite ManagementSource Document VerificationCRF Review
EVERSANA

Diagnostic Specialist - Appalachia

🕒 19 days ago
EVERSANA👥 1001 - 5000 employees🏢 Pharmaceuticals

Educate healthcare providers and diagnostic stakeholders on genetic testing programs, IRD gene panels, and testing best practices while contributing regional insights to diagnostic strategy.

Genetic TestingDiagnostic StrategyGenotypingIRD Gene Panels
Allucent

Clinical Research Associate

🕒 21 days ago
Allucent👥 501 - 1000 employees🏢 Pharmaceuticals

Independently lead clinical trial site monitoring from initiation through close-out, ensuring regulatory compliance, data quality, and patient safety while building investigator relationships and mentoring junior CRAs.

Clinical Trial MonitoringSite Initiation VisitsRoutine Monitoring VisitsClose-out Visits
PSI CRO

Senior Clinical Research Associate

🕒 23 days ago
PSI CRO👥 1001 - 5000 employees🏢 Pharmaceuticals

Conduct onsite clinical study monitoring and manage site relationships, timelines, and compliance across Phase II and/or III research, supporting study startup, data quality, and regulatory submissions.

Clinical Research MonitoringOnsite Monitoring VisitsStudy StartupCRF Review
PSI CRO

Senior Clinical Research Associate

🕒 25 days ago
PSI CRO👥 1001 - 5000 employees🏢 Pharmaceuticals

Leads site monitoring and communication for clinical research projects, overseeing study timelines, data quality, compliance, and stakeholder relationships across therapeutic indications.

Clinical Research MonitoringOnsite Monitoring VisitsClinical Trial Site ManagementCRF Review
PSI CRO

Senior Clinical Research Associate

🕒 25 days ago
PSI CRO👥 1001 - 5000 employees🏢 Pharmaceuticals

Conducts and reports clinical study monitoring visits, manages site communications and study documentation, and supports feasibility research, regulatory submissions, audits, and inspections across therapeutic indications.

Clinical ResearchClinical Study MonitoringSite ManagementCRF Review
Ergomed

Clinical Research Associate II / Senior CRA

🕒 28 days ago
Ergomed👥 501 - 1000 employees🏢 Biotechnology

Conducts on-site and remote monitoring visits for clinical trials, verifies investigator and site readiness, trains site staff, and supports regulatory submissions to help maintain study quality and progress.

Clinical Trial MonitoringPhase 2/3 TrialsOncologyRare Disease
Ergomed

Senior Benefit/Risk Associate

🕒 29 days ago
Ergomed👥 501 - 1000 employees🏢 Biotechnology

Supports pharmacovigilance signal management by reviewing safety data, evaluating potential signals, drafting complex reports, and helping coordinate regulatory communications to protect patient safety.

PharmacovigilanceSignal DetectionSignal ManagementSafety Data Review
Ergomed

Senior Benefit/Risk Associate

📅 Sep 23
Ergomed👥 501 - 1000 employees🏢 Biotechnology

Supports contracted pharmacovigilance work by detecting and evaluating potential safety signals, drafting complex reports, and coordinating regulatory communications to help protect patients.

PharmacovigilanceSignal DetectionSignal ManagementSignal Detection Reporting

Leads monitoring and site management for complex clinical studies, ensuring protocol compliance, data quality, and participant safety while identifying risks, recommending corrective actions, and mentoring junior clinical operations staff.

Clinical Site MonitoringRisk-based MonitoringSource Data VerificationSource Data Review
Dane Street

Physician Reviewer - Board Certified Behavioral Analyst (BCBA-D)

📅 Sep 18
Dane Street👥 201 - 500 employees🏢 Insurance🤝 B2B

As a Board Certified Behavioral Analyst (BCBA-D), you will conduct thorough reviews of clinical cases, evaluate medical records, and provide clinical summaries as an independent contractor.

Behavioral AnalysisClinical ReviewMedical Record EvaluationPeer Communication
PSI CRO

Senior Clinical Research Associate

📅 Sep 15
PSI CRO👥 1001 - 5000 employees🏢 Pharmaceuticals

Leads clinical site monitoring for Phase II and III studies, managing site relationships, monitoring visits, study timelines, and quality oversight while protecting participant safety and ensuring reliable data.

Clinical Research MonitoringOn-site Monitoring VisitsCRF ReviewSource Document Verification
Dane Street

Orthopedic Spine Surgeon - Clinical Reviewer | Tennessee (Remote)

📅 Sep 14
Dane Street👥 201 - 500 employees🏢 Insurance🤝 B2B

As a Board-Certified Orthopedic Spine Surgeon, you will conduct comprehensive reviews of clinical cases, providing objective, evidence-based medical advisory opinions remotely.

Orthopedic SurgerySpine SurgerySpinal ConditionsOrthopedic Procedures
Corcept Therapeutics

Senior Regional Clinical Research Associate

📅 Aug 6
Corcept Therapeutics👥 501 - 1000 employees🏢 Biotechnology

Oversees clinical trial sites from qualification through close-out, serving as the primary liaison and ensuring recruitment, documentation, safety reporting, and study conduct meet GCP, ICH, and company requirements.

Clinical Trial MonitoringClinical Site ManagementGCPICH Guidelines
Mediantechnologies

Directeur de la Génération de Preuves

📅 Jun 29
Mediantechnologies👥 51 - 200 employees🏢 Computer Software

Le Directeur de la Génération de Preuves conçoit et supervise des études cliniques et du monde réel pour soutenir l’approbation réglementaire, le remboursement et l’adoption de logiciels en tant que dispositifs médicaux.

Épidémiologie CliniqueBiostatistiquePreuves Du Monde Réel (rwe)HEOR
Allucent

Clinical Research Associate (Germany)

📅 May 4
Allucent👥 501 - 1000 employees🏢 Pharmaceuticals

Independently oversee clinical trial monitoring across study phases, manage investigator-site relationships, and support regulatory and site-startup activities while protecting trial integrity and patient safety.

📍 🇩🇪 Germany - Remote💼 Full-Time🎸 Senior🧫 Clinical Research Specialist📢 🇬🇧 English Required📢 🇩🇪 German Required
Clinical Trial MonitoringSite InitiationRoutine MonitoringClose-out Visits

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