Research Coordinators
2,014 open positions
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Case Manager Schwerpunkt Participant Service / Studienteilnehmerservice in einer Clinical (m/w/d) Profil Institut für Stoffwechselforschung GmbHNeuss, NORDRHEIN_WESTFALEN 1mo Coordinate and support clinical trial participants in a Clinical Research Unit, ensuring their comfort and logistical needs during visits.
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Assistant CRA - FSO ThermoFisher ScientificRemote 1mo Support Clinical Research Associates with site preparedness, logistical monitoring, and administrative tasks across clinical trials.
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Clinical Project Coordinator (SEARCH-C Cambodia)- The Kirby Institute UnswSydney, New South Wales 1mo Coordinate the development, implementation, and monitoring of clinical research projects within the Viral Hepatitis Clinical Research Program, with a primary focus on SEARCH-C Cambodia.
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Clinical Project Administrator Linear Clinical ResearchNedlands, Western Australia 1mo Coordinate cancer clinical trials by managing projects, ensuring compliance, and liaising with sponsors, clinicians, and participants.
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Clinical Research Technician New Zealand Clinical ResearchSydenham, Christchurch 1mo Assist nursing staff with clinical procedures including vital signs, ECGs, and urinalysis per study protocols, while entering accurate real-time data into participant records.
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Programm Management / Studienkoordination (m/w/d) Universitätsklinikum Bonn'Bonn, NORDRHEIN_WESTFALEN 1mo Managing and coordinating large-scale scientific studies, including planning, initiation, execution, and network coordination within a university hospital setting.
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Clinical Research Trials Coordinator - Jreissati Pancreatic Centre EpworthRichmond, Victoria $16k1mo Coordinate clinical research activities across the trial lifecycle for pancreatic cancer studies, ensuring compliance with protocols and regulatory requirements.
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Senior Regulatory and Start Up Specialist (Argentina) PrecisionmedicinegroupRemote 1mo Senior Regulatory and Start Up Specialist responsible for clinical trial submission to Competent Authorities and IRB/Ethics Committees, Informed Consent Form review, Essential Document collection, and supporting site contract management in Argentina.
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Clinical Trial Associate PathAIRemote $64k1mo Monitor clinical trial lab services, engage with investigator sites, and support Clinical Trial Managers to ensure successful completion of clinical studies with a lab services component.
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Regulatory Officer Psi-CroMilan, Lombardy, it €36k1mo Facilitate the start of research projects for novel medicinal products by managing regulatory submissions and coordinating with authorities and project teams.
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Personen mit medizin. Berufsausbildung als Study Nurse / Studienassistenz (w/m/d) für die Onkologie Universitätsmedizin GöttingenGöttingen, NIEDERSACHSEN 1mo Support the preparation and execution of oncological clinical trials in collaboration with study physicians and study coordination.
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Manager, Clinical Research Financial Operations UtaustinAUSTIN, TX, US 1mo Manages day-to-day centralized clinical research operations, overseeing study start-up, trial coordination, regulatory workflows, and research coordinator pools to ensure efficient execution of clinical trials.
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FSP Clinical Trial Coordinator II ThermofisherMexico City, Mexico 1mo Coordinate and facilitate clinical trial activities, serving as a cross-functional liaison and study lead for assigned trials.
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Clinical Research Coordinator 1 - Cancer Survivorship, Lifestyle & Behavioral Research UmiamiMiami, FL, US 1mo Entry-level clinical research professional supporting oncology-focused lifestyle and behavioral research studies by managing participant screening, data collection, and protocol implementation.
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Study Nurse - Dr. Senckenbergischen Institut für Neuroonkologie Universitätsklinikum FrankfurtFrankfurt am Main, HESSEN 1mo Coordinate care and logistics for clinical trial patients in a neuro-oncology setting, including blood draws, therapy administration, and documentation.
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Clinical Project Coordinator/Clinical Trial Assistant Join The CTI TeamSydney, New South Wales 1mo Support Clinical Project Manager/Director in managing all phases of clinical projects, including site start-up, subject enrollment, document maintenance, and audit support.
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Legal Specialist (Argentina) InderoRemote 1mo Legal Specialist supporting clinical research operations with contract management, regulatory compliance, and legal documentation.
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Entry Clinical Trials Feasibility Specialist MedpaceCincinnati, Ohio 1mo Coordinate feasibility assessments and deliver accurate data to support country selection and enrollment planning for global clinical trials.
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Research Nurse Coordinator II - Center for Clinical Studies WustlWashington University Medical Campus, US $65k1mo Lead person on clinical research projects, coordinating subject enrollment, ensuring protocol adherence, and providing direct patient care.
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Clinical Research Coordinator - Full Time - Day Shift - West Penn HighmarkhealthPittsburgh PA, 15224, West Penn 4800 Friendship Ave, US 1mo Plans, coordinates, and manages clinical trial activities from initiation to completion, ensuring patient safety and regulatory compliance.
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Human Subject Research Spec I Pediatric Allergy RochesterSchool of Medicine and Dentistry, US 1mo Coordinates administrative and logistical details for pediatric allergy and immunology human subject research, including recruitment, sample processing, and study visits.
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Study Nurse in der Diabetologie (m/w/d)↗ Lmu Klinikum MünchenMünchen, BY, DE 1mo Conducting prospective clinical and drug studies in the field of diabetes mellitus for early detection, prevention, and treatment.
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IRB Analyst II SluSLU Saint Louis, MO, US 1mo Coordinates daily activities for processing research protocols and managing the Institutional Review Board (IRB) and Human Research Protection Program (HRPP) to ensure compliance with federal regulations and protect human subjects.
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Study Nurse / Studienassistenz (d/w/m) Pneumologie (Emphysem / COPD) Charité Universitätsmedizin Berlin KdöRBerlin, BERLIN 1mo Support clinical trials for patients with chronic respiratory diseases (emphysema/COPD) in an outpatient, inpatient, and intensive care setting at a university hospital.
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Controller (m/w/d) acromion GmbH AuftragsforschungsinstitutFrechen, NORDRHEIN_WESTFALEN 1mo Implementing and managing a new controlling software system (Trialytix) for clinical research projects, including data mapping, user administration, reporting, and project forecasting.
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Associate Director, Patient Engagement CslEMEA, GB, Berkshire, Maidenhead, CSL Behring 1mo Partner with patient organizations and advocacy groups to embed patient perspectives into clinical trial design, protocol development, and recruitment strategies.
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Site Activation Coordinator, import/export IqviaBuenos Aires, Argentina 1mo Support Argentina in import/export activities for clinical trial site activation, ensuring regulatory compliance and document accuracy.
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Studienassistenz (M/W/D) für den Lehrstuhl für Frauenheilkunde... Universitätsklinikum RegensburgRegensburg, BAYERN 1mo Support clinical trials for the Department of Gynecology and Obstetrics by conducting studies, coordinating logistics, and managing patient data.
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Research Assistant - Clinical ArchildrensLittle Rock, US 1mo Support clinical trials, federal/nonfederal grants, and community-based projects by managing data collection, participant recruitment, and regulatory compliance.
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Clinical Research Coordinator AoncologyUS-FL-Naples 1mo Coordinate care for patients on clinical research protocols and manage the implementation of Phase 4 and observational/registry trials under medical supervision.
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?Clinical Research Coordinator↗ Katy, TX, US 1mo Coordinate and support all aspects of clinical trials and research studies, including subject recruitment, data collection, regulatory compliance, and specimen handling.
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Research Scientist (Grade 2) Department of Nephrology St Vincent’s Health AustraliaMelbourne, Victoria $94k1mo Provides research coordination and administrative support for clinical research within the Nephrology Research Unit, supporting participant recruitment, study coordination, and regulatory compliance.
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Nurse Practitioner or Physician Assistant (Sub Investigator) - Part-time M3usaLos Angeles, CA, us $104k1mo Ensures compliance with clinical trial regulations and protocols while conducting patient visits and collecting data for research studies.
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Study Support Specialist (GLP studies – Product Safety Labs) EurofinsBengaluru, KA, in 1mo Support Study Directors in managing GLP-compliant pre-clinical studies, ensuring data quality, regulatory compliance, and on-time delivery of study documentation and results.
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