🕒 4 days ago
Perform and support pharmacovigilance signal management, from reviewing safety data and evaluating potential signals to drafting reports and supporting regulatory communications.
Remote Clinical Research Specialist Jobs
Search 51 active remote clinical research specialist jobs. No recruiters, no spam - just real jobs from real companies.
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🕒 5 days ago
Conducts site monitoring across clinical studies, ensuring protocol and regulatory compliance while overseeing recruitment, data quality, site risks, trial documentation, and investigator collaboration.
Senior Clinical Research Associate - Cardiovascular (Bilingual-English/Spanish) (Remote)
🕒 5 days ago
Msd👥 51 - 200 employees🏢 Pharmaceuticals
🕒 5 days ago
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
Speech-Language Pathologist (SLP) - Clinical Reviewer (Pennsylvania)
🕒 5 days ago
Dane Street👥 201 - 500 employees🏢 Insurance🤝 B2B
🕒 5 days ago
Review speech-language pathology records, assessments, and treatment plans, preparing objective, evidence-based clinical summaries and advisory opinions on care, clinical standards, and medical necessity.
🕒 6 days ago
Manage and develop a team of 6–14 Clinical Research Associates, supporting consistent trial monitoring, site performance, regulatory compliance, and effective resource planning.
📍 🇺🇸 New Jersey Rahway - Remote💰 $142.4k - $224.1k / year💼 Full-Time🎙️ Leadership📋 Manager📢 🇬🇧 English Required
🕒 6 days ago
Leads and contributes to hematology and oncology clinical study design and execution, partnering across teams to author regulatory documents, interpret clinical data, monitor safety, and support study delivery and scientific communications.
📍 🇺🇸 United States - Remote💰 $192k - $239k / year💼 Full-Time🎙️ Leadership🧫 Clinical Research Specialist
Sample Collector / Phlebotomist (Ad Hoc)
🕒 6 days ago
Eurofins👥 5001 - 10,000 employees🏢 Biotechnology
🕒 6 days ago
Collect hair, nail, blood and DNA samples at pre-booked appointments, using safe procedures and maintaining quality standards, client relationships and documentation that may support legal proceedings.
Clinical Research Associate II / Senior CRA (Spanish, Portuguese & English fluency)
🕒 6 days ago
Ergomed👥 501 - 1000 employees🏢 Biotechnology
🕒 6 days ago
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 Research Associate II / Senior CRA (Spanish, Portuguese & English fluency)
🕒 6 days ago
Ergomed👥 501 - 1000 employees🏢 Biotechnology
🕒 6 days ago
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
Sr Clinical Research Associate Contractor (Belarus)
🕒 8 days ago
Allucent👥 501 - 1000 employees🏢 Pharmaceuticals
🕒 8 days ago
Independently oversee clinical trial monitoring from site initiation through close-out, maintaining GCP and regulatory compliance, strong investigator relationships, data quality, and trial integrity.
🕒 9 days ago
Manage individual case safety reports and related pharmacovigilance activities, ensuring regulatory and client-specific compliance while supporting patient safety, reporting, and local safety processes.
Site Manager (clinical research, local site coordinator role)
🕒 11 days ago
Ergomed👥 501 - 1000 employees🏢 Biotechnology
🕒 11 days ago
The Site Manager facilitates clinical studies by providing patient-related site support, ensuring compliance with protocols, and optimizing site staff performance.
Site Manager (clinical research, local site coordinator role)
🕒 11 days ago
Ergomed👥 501 - 1000 employees🏢 Biotechnology
🕒 11 days ago
The Site Manager facilitates clinical studies by providing patient-related site support and ensuring compliance with protocols and regulatory requirements.
📍 🇩🇪 Frankfurt am Main - Remote💼 Full-Time🎹 Mid-level📋 Manager📢 🇬🇧 English Required📢 🇩🇪 German Required
Clinical Research Associate II / Senior CRA (French Speaking)
🕒 11 days ago
Ergomed👥 501 - 1000 employees🏢 Biotechnology
🕒 11 days ago
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
Business Development Director (Clinical Research), UK and Nordics
🕒 11 days ago
Ergomed👥 501 - 1000 employees🏢 Biotechnology
🕒 11 days ago
The Business Development Director will lead strategic sales initiatives, develop account strategies, and identify new business opportunities within the clinical research sector.
🕒 12 days ago
Manage clinical trial activities across global projects, conducting site monitoring and supporting study startup while maintaining site relationships, patient safety, data quality, and compliance with study standards.
🕒 12 days ago
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.
🕒 12 days ago
The Director, Clinical Development Research Scientist will lead clinical trials and provide strategic leadership in advancing Avalyn's IPF/ILD clinical development programs.
🕒 14 days ago
Conduct site monitoring across clinical studies, serving as the link between project teams, sponsors, and sites while protecting data integrity, protocol compliance, and study timelines.
📍 🇺🇸 United States - Remote💼 Full-Time🎹 Mid-level🧫 Clinical Research Specialist📢 🇬🇧 English Required
🕒 16 days ago
Educate healthcare providers and diagnostic stakeholders on genetic testing programs, IRD gene panels, and testing best practices while contributing regional insights to diagnostic strategy.
Sr. Clinical Research Associate/Clinical trial Manager
🕒 18 days ago
BridgeBio Pharma👥 501 - 1000 employees🏢 Biotechnology
🕒 18 days ago
As a Sr. Clinical Research Associate/Clinical Trial Manager, you will lead the operational management of clinical studies, ensuring compliance with protocols and regulations while collaborating with cross-functional teams.
🕒 18 days ago
Conduct onsite monitoring across clinical studies, oversee site communication and study progress, review clinical data, support study startup and regulatory submissions, and contribute to audits and inspections.
🕒 18 days ago
Conduct onsite monitoring visits across clinical studies, manage site communications and study documentation, and support study startup, feasibility, audits, and inspections while maintaining high quality standards.
🕒 19 days ago
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.
