Perform and support pharmacovigilance signal management, from reviewing safety data and evaluating potential signals to drafting reports and supporting regulatory communications.
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.
23 total jobs
1 new job this week
Senior Clinical Research Associate - Cardiovascular (Bilingual-English/Spanish) (Remote)
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.
Clinical Research Associate II / Senior CRA (Spanish, Portuguese & English fluency)
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.
Clinical Research Associate II / Senior CRA (Spanish, Portuguese & English fluency)
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.
Sr Clinical Research Associate Contractor (Belarus)
Independently oversee clinical trial monitoring from site initiation through close-out, maintaining GCP and regulatory compliance, strong investigator relationships, data quality, and trial integrity.
Manage individual case safety reports and related pharmacovigilance activities, ensuring regulatory and client-specific compliance while supporting patient safety, reporting, and local safety processes.
Clinical Research Associate II / Senior CRA (French Speaking)
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.
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.
Educate healthcare providers and diagnostic stakeholders on genetic testing programs, IRD gene panels, and testing best practices while contributing regional insights to diagnostic strategy.
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.
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.
Leads site monitoring and communication for clinical research projects, overseeing study timelines, data quality, compliance, and stakeholder relationships across therapeutic indications.
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 Research Associate II / Senior CRA
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.
Supports pharmacovigilance signal management by reviewing safety data, evaluating potential signals, drafting complex reports, and helping coordinate regulatory communications to protect patient safety.
Supports contracted pharmacovigilance work by detecting and evaluating potential safety signals, drafting complex reports, and coordinating regulatory communications to help protect patients.
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.
Physician Reviewer - Board Certified Behavioral Analyst (BCBA-D)
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.
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.
Orthopedic Spine Surgeon - Clinical Reviewer | Tennessee (Remote)
As a Board-Certified Orthopedic Spine Surgeon, you will conduct comprehensive reviews of clinical cases, providing objective, evidence-based medical advisory opinions remotely.
Senior Regional Clinical Research Associate
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.
Directeur de la Génération de Preuves
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.
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.
