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Healthcare
› Research Coordinators
Research Coordinators
1,040 open positions
Associate Project Manager - Labs
Thermofisher
Remote
$51k–$51k
1d
Liaise with operational departments, affiliates, and sponsors to support the identification, evaluation, and resolution of shipments for clinical trial protocols and study programs.
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Clinical Research Coordinator 1
Umiami
Miami, FL, US
1d
Senior Clinical Research Coordinator leading the planning, implementation, monitoring, and evaluation of multiple complex clinical research protocols at an academic medical center.
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Senior Clinical Trial Assistant
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Iqvia
40, TH
1d
Administrative support for clinical research teams ensuring accurate Trial Master File delivery, document management, and clinical data flow coordination.
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Clinical Research Coordinator 1
Umiami
Miami, FL, US
1d
Entry-level clinical research professional managing data and implementing simple clinical research protocols.
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Sr Site Activation Coordinator
Iqvia
Durham, North Carolina, United States of America
$36k–$36k
1d
Execute feasibility, site activation, and maintenance activities for investigative sites in clinical studies, ensuring regulatory compliance and document accuracy.
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Centralized Clinical Research Operations Analyst II
Utaustin
AUSTIN, TX, US
1d
Supports advanced operational activities, performance reporting, workflow optimization, and research systems coordination for the clinical trial lifecycle.
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Clinical Research Coordinator
Utaustin
AUSTIN, TX, US
$53k–$53k
1d
Coordinate and manage oncology clinical trials, ensuring regulatory compliance and data integrity for cancer research studies.
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Nurse Practitioner-Per Diem
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Albert Einstein College of Medicine
Bronx, NY, US
$122k–$122k
1d
Assess, plan, and implement observational and clinical research protocols for study subjects in therapeutic and non-therapeutic research studies.
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Study Nurse (m/w/d)
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Marienhaus Holding
Neustadt an der Weinstraße, RP, DE
1d
Clinical research coordination and participant management for oncology studies at an academic hospital.
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Study Nurse
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Praxis Dr. Heinrich
Fürstenwalde/Spree, BB, DE
$44k–$44k
1d
Care and monitoring of study participants and ensuring adherence to study protocols in clinical trials.
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Clinical Research Coordinator 2
Umiami
Miami, FL, US
1d
Mid-level clinical research professional assisting in planning, coordinating, implementing, monitoring, and evaluating specific clinical research studies from initiation to close-out.
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Co-op, Patient Communications & Innovation
Biibhr
Cambridge, MA, US
$0k–$0k
1d
Support innovative projects to improve the clarity, accessibility, and usability of patient-facing clinical research materials.
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Sr Site Activation Coordinator
Iqvia
Durham, North Carolina, United States of America
$41k–$41k
1d
Execute feasibility, site activation, and maintenance activities for investigative sites in clinical studies, ensuring document completeness and regulatory compliance.
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Contract Coordinator - FSP RSU Team
Iqvia
São Paulo, Brazil
1d
Perform site activation activities for clinical research studies, ensuring regulatory and contractual document compliance and accuracy.
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Sr CTA - Sponsor Dedicated - Israel
Iqvia
Netanya, Israel
1d
Administrative support for Clinical Research Associates and Regulatory teams to ensure accurate Trial Master File delivery and clinical documentation management.
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Lead Clinical Research Coordinator
Iqvia
Remote
$49k–$49k
1d
Coordinate and perform remote clinical activities to collect, record, report, and interpret patient data for clinical research studies in compliance with protocols and GCP.
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Intern - Country Site Activation
Iqvia
Madrid, Spain
1d
Support clinical trial start-up activities by assisting with regulatory, contractual, and document management processes for site activation.
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Senior Clinical Trial Coordinator
KG Talent
Sydney, New South Wales
1d
Senior Clinical Trial Coordinator responsible for end-to-end coordination, delivery, and compliance of multiple clinical trials within a medical centre's Clinical Research Unit.
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Studienassistenz (Study Nurse) (all genders) für die Klinik für Intensivmedizin
↗
Uke - Universitätsklinikum Hamburg-Eppendorf
Hamburg, HH, DE
$43k–$43k
2d
Central coordination and data management for clinical trials in the Intensive Care Unit, ensuring compliance with GCP and regulatory standards.
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Research Nurse Specialist 2 - Rheumatology
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Vanderbilt Health
Nashville, TN, US
2d
Ensures integrity and quality of clinical research trials in rheumatology/immunology, managing recruitment, enrollment, and protocol compliance.
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Clinical Specialist, Translational Medicine
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Neurona Therapeutics
South San Francisco, CA, US
2d
Guide administration of cellular therapeutics during patient procedure enrollment in operating rooms for a Pivotal Phase III Clinical Trial.
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Coordinator Research - Research Industry
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CHRISTUS Health
Tyler, TX, US
2d
Administrative and clinical support for research protocols in outpatient clinics and inpatient units, including patient screening, consent coordination, and biospecimen handling.
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Provisional Fellow
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NSW Health
Campbelltown, NSW, AU
$118k–$118k
2d
Sub-Principal Investigator overseeing gastroenterology clinical trials, managing patient enrollment, medical assessments, and trial documentation.
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Ethics Submission Specialist (Clinical Research)
Cancer Trials Australia
Remote
$80k–$80k
2d
Coordinate ethics and governance submissions for clinical trials to ensure effective and timely approval and implementation.
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Ethics Submission Specialist (Clinical Research) – Remote
Cancer Trials Australia
Remote
$80k–$80k
2d
Coordinate ethics and governance submissions for clinical trial study start-up to ensure timely approval and implementation.
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Clinical Research Associate - Freshers
ClinoGenesis Research Institute
Remote
3d
Assist with on-site coordination of clinical trial activities under supervision, maintain essential documents and site files, and support investigators in protocol compliance.
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Senior Clinical Trial Associate
Jobgether
Remote
$85k–$85k
3d
Supports the planning, execution, and closeout of clinical studies in a regulated environment, ensuring compliance with protocols and GCP.
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Studienassistenz (Study Nurse) (all genders) - Multiple Sklerose Ambulanz und Tagesklinik - Klinik für Neurologie
Universitätsklinikum Hamburg-Eppendorf
Hamburg, Deutschland
$45k–$45k
3d
Clinical study support for Multiple Sclerosis, Neuromyelitis optica, and Myasthenia gravis patients in an outpatient and day clinic setting.
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Clinical Trial Assistant - Based in Spain
Iqvia
España
3d
Administrative support for Clinical Research Associates and Regulatory teams to ensure accurate Trial Master File delivery and site compliance tracking.
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CTMS Operations Analyst
Jobgether
Remote
3d
Support clinical research operations through CTMS configuration, quality control, operational reporting, and user support to ensure study readiness and compliance.
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Clinical Research Medical Assistant
Delricht Research
Atlanta, GA
3d
Deliver excellent patient experience and drive accurate, efficient study execution across clinics for clinical trials.
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Research Regulatory Coordinator
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Palm Medical Group
Las Vegas, NV, US
$0k–$0k
3d
Primary liaison between clinical research sites and study sponsors, ensuring trial compliance and managing regulatory documentation.
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Study Nurse; Studienassistentin/Studienassistent
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Lungenfachpraxis Liefring/Teber
Berlin, BE, DE
3d
Temporary maternity cover for a study nurse role supporting clinical trials in outpatient pulmonology (asthma and COPD).
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Clinical Research Coordinator II : Research Cancer
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Hoag Health System
Irvine, CA, US
3d
Manage FDA-regulated clinical research trials for cancer studies, including patient recruitment, data collection, and regulatory compliance.
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Clinical Research Coordinator - II
↗
Concord Retreat
Burke, VA, US
$52k–$52k
3d
Coordinate study-related activities for patients enrolled in internal medicine research studies including hypertension, diabetes, and obesity.
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Clinical Research Associate
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Charak Hospital & Research Centre
UP, IN
$180k–$180k
3d
Coordinate and manage all phases of clinical trials at a hospital, ensuring compliance with ICH-GCP and ethical guidelines while managing documentation and patient recruitment.
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Clinical Trial Associate I
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Ora
Remote, US
3d
Supports Project Managers and study teams in conducting clinical ophthalmic studies, ensuring protocol adherence and regulatory compliance across study phases.
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Sr. Clinical Research Project Coordinator (Clinical Research Coordinator Experienced)
Medpace
Denver, Colorado
$75k–$75k
4d
Full-time Project Coordinator supporting clinical trial management for biotech and pharmaceutical clients across multiple therapeutic areas.
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Entry-Level Research Project Coordinator
Medpace
Cincinnati, Ohio
4d
Support Clinical Trial Management teams in executing day-to-day operational tasks for biotech and pharmaceutical clinical trials.
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Clinical Research Project Coordinator - Ophthalmology
Medpace
Cincinnati, Ohio
4d
Full-time Project Coordinator supporting clinical trial management for biotech and pharmaceutical clients, focusing on tasks like status reporting, regulatory filing oversight, and supply management.
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Clinical Research Project Coordinator - Oncology
Medpace
Cincinnati, Ohio
4d
Support clinical trial management for Oncology/Hematology studies by coordinating tasks, managing supplies, and maintaining project timelines.
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Clinical Research Project Coordinator - Immunology
Medpace
Cincinnati, Ohio
4d
Support clinical trial management by coordinating tasks, maintaining timelines, and ensuring quality control of regulatory filings for biotech and pharmaceutical clients.
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Clinical Research Project Coordinator - Infectious Disease
Medpace
Cincinnati, Ohio
4d
Full-time office-based Project Coordinator supporting Clinical Trial Management teams in managing day-to-day trial operations, timelines, and regulatory filings.
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Clinical Research Project Coordinator - Cardiovascular, Renal, Metabolic
Medpace
Cincinnati, Ohio
4d
Full-time Project Coordinator supporting clinical trial management for Cardiovascular, Renal, and Metabolic therapeutic areas.
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Study Start-Up Coordinator- PharmD
Medpace
Cincinnati, Ohio
4d
Coordinate regulatory submissions and site activation for clinical trials by communicating with research sites and managing trial documentation.
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Study Start-Up Coordinator (CRC Experience)
Medpace
Cincinnati, Ohio
4d
Coordinate study start-up activities by communicating with research sites to collect essential documents and assemble regulatory submissions for clinical trials.
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Experienced Study Start-Up Research Coordinator
Medpace
Denver, Colorado
$40k–$40k
4d
Coordinate regulatory submissions and site activation for clinical trials by managing documentation, timelines, and communications with research sites.
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Study Start-Up Coordinator – Clinical Research Coordinator Experience
Medpace
Irving (Dallas), Texas
4d
Coordinate regulatory submissions and site activation for clinical trials by managing documentation and timelines with research sites.
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Entry-Level TMF Operations Associate
Medpace
Cincinnati, Ohio
4d
Manage electronic filing systems for clinical trial documentation, ensuring documents meet quality standards and preparing them for shipment.
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Entry-Level Trial Master File (TMF) Specialist
Medpace
Cincinnati, Ohio
4d
Manage the Trial Master File (TMF) to ensure data integrity and support the successful execution of clinical trials for drug and device development.
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