Research Coordinators
979 open positions
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Clinical Research Data Specialist I UscLos Angeles, CA - Health Sciences Campus, US $0k–$0k1mo Manage high-quality clinical research data for urologic oncology studies, including patient screening, data collection, and database maintenance.
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Research Technician (Phlebotomist) - Per Diem ThermofisherLas Vegas, Nevada, USA $35k–$35k1mo Support Phase I and IB clinical trials by performing phlebotomy, vital signs monitoring, ECGs, and other technical procedures on study subjects.
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Senior Associate I, TMF Operations - UK - Remote↗ Worldwide Clinical TrialsRemote 1mo Manage Trial Master File (TMF) operations including setup, maintenance, archiving, and quality control for clinical studies to ensure regulatory compliance.
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Clinical Trial Liaison Psi-CroBudapest, hu 1mo Act as a specialized liaison to assist clinical trial sites with protocol-tailored approaches to increase efficiency in patient identification, recruitment, and retention.
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Clinical Site Associate↗ ICON PlcSão Paulo, São Paulo, Brazil 1mo Assist with the design and analysis of clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments.
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Clinical Research Coordinator EcpcareersOphthalmology Associates 1mo Manage daily operations of clinical trials involving human subjects, ensuring quality data collection, participant recruitment, and adherence to study protocols.
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Specialist, Human Genetic Resources (HGR) Management AbbVieShanghai, Shanghai, cn 1mo Execute Human Genetic Resources (HGR) application activities, prepare and submit regulatory dossiers, and ensure compliance with local regulations and ICH GCP standards for clinical studies in China.
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Clinical Research Coordinator, Autism Research Simonsfoundation160 Fifth Avenue, New York, NY $72k–$72k1mo Support data activities for clinical cohorts and biorepositories in autism research, ensuring quality assurance, standardization, and release of datasets.
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Regulatory and Site Start Up Specialist Precision Medicine GroupRemote, Taiwan 1mo Ensure site activation readiness and manage regulatory submissions for clinical trials in oncology and rare diseases.
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CPQuali - Técnico de Enfermagem QimaSão Paulo, SP, br $0k–$0k1mo Support clinical studies by performing blood draws and providing care to study participants.
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Técnico determinación Protección Solar EurofinsBarcelona, CT, es 1mo Conduct and coordinate clinical studies for sunscreen protection factors, including inter-laboratory studies, in compliance with ISO regulations.
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Research Pharmacy Technician (CPhT) - IDS OsuJames Cancer Hospital and Solove Research Institute 1mo Manage investigational products and provide technical assistance for clinical trial protocols under a licensed pharmacist.
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Clinical Research Associate I AbbottUnited States - California - Alameda $74k–$74k1mo Ensure quality, accuracy, and integrity of clinical trial data throughout the full lifecycle of internal medical device and in-vitro diagnostics studies.
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Manager, Clinical Research-Immunology Early MsdCHN - Shanghai - Shanghai (Tower A), CN 1mo Conduct early clinical studies in the Immunology field.
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Clinical Research Project Manager UchicagoChicago, IL 1mo Independently manages the collection, documentation, analysis of clinical trial data, and reporting of clinical research data for high-complexity studies.
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Gestionnaire de cas bilingue/ Bilingual Caseworker MyhrabcRemote 1mo Bilingual caseworker supporting patient access, clinical monitoring, and data collection for pharmaceutical programs in Canada.
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Clinical Trial Associate (Associate, Rater Services) CogstateincRemote $65k–$65k1mo Support the timely delivery of the Cogstate Rater Training Program and oversee quality management for clinical trial programs.
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Clinical Research Coordinator I, Oncology RchMain Campus - Orange $0k–$0k1mo Manage pediatric clinical research studies by coordinating protocols, recruiting participants, collecting data/specimens, and maintaining regulatory compliance.
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Program Manager MassgeneralbrighamBoston-MA 1mo Manages the day-to-day operational implementation of a clinical research portfolio, supervising research staff and ensuring adherence to study protocols and timelines.
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Sample Management Coordinator 1 IconUS, Farmingdale, NY $39k–$39k2mo Coordinating the receipt, tracking, storage, and distribution of clinical trial biological samples to ensure accurate and timely management for research studies.
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Sample Coordinator (Sample Management) LabcorpSingapore 2mo Coordinate the receipt, tracking, processing, shipment, and documentation of clinical trial samples to ensure compliance with study protocols and quality standards.
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Research Compliance Specialist II HuronRemote $72k–$72k2mo Reviews and processes Institutional Review Board (IRB) submissions and Conflict of Interest (COI) disclosures for academic medical centers, hospitals, and research universities.
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Clinical Trial Associate GeneratebiomedicinesSomerville, MA $79k–$79k2mo Support execution of Phase 1-3 clinical trials, ensuring compliance with GCP standards and maintaining inspection-readiness for regulatory submissions.
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RN Clinical Research Structural Heart SpectrumhealthGrand Rapids, MI 2mo Coordinates and implements clinical research studies for structural heart and vascular procedures, managing patient enrollment, data collection, and regulatory compliance.
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Manager, Clinical Research RochesterJames P. Wilmot Cancer Center $71k–$71k2mo Manage the daily operations of a Clinical Trials Office, oversee study personnel, and ensure compliance with Good Clinical Practices and regulatory standards for radiation oncology research.
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Program Manager, HRPP Regulatory Operations SluFloor 02-Schwitalla Hall 2mo Execute education programs, conduct pre-submission intake reviews, and provide IRB review and quality assurance support for the Human Research Protection Program (HRPP).
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Clinical Research Manager (SOM Pediatric Endocrinology) JhuBaltimore, MD, United States $56k–$56k2mo Manage administrative and scientific implementation of complex clinical protocols and multi-center studies in pediatric endocrinology, focusing on obesity, insulin resistance, and type 2 diabetes.
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Clinical Writer I SgsRichardson, TX, us 2mo Drafts and reviews clinical study protocols and reports for cosmetics and other claims, adhering to ICH and GCP guidelines.
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Heart Institute - Clinical Research Assoc I/CPT, Susan Cheng Team↗ Cedars-SinaiLos Angeles, CA 2mo Supports the coordination and implementation of noncomplex clinical research studies by collecting data, managing patient scheduling, and ensuring regulatory compliance.
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