NewRN, Clinical Research Nurse Coordinator Trinity Health CorporationRN, Clinical Research Nurse CoordinatorSilver Spring, MD$77,334–$116,000 / yearGeneral Summary: The Clinical Research Nurse Coordinator leads, manages and coordinates research programs and studies for the Clinical Research Program and physician Principal Investigators. Holy Cross Health has earned numerous national awards, clinical designations, and accreditations across a wide range of specialties for providing innovative, high-quality health care services.
Clinical Research Coordinator I CBH Health LLCClinical Research Coordinator IGaithersburg, MD$26.90–$34.35 / hourPart timeRecently acquired by BayPine Capital Partners, our research sites provide unparalleled medical and scientific support in the design and execution of clinical trials. Responsible for assisting with coordinating clinical trials with the strictest adherence to ICH (International Conference on Harmonization), GCP (Good Clinical Practices), protocol, and company guidelines, regulations, and policies.
Clinical Research Coordinator II - Annapolis/Columbia Maryland OncologyClinical Research Coordinator II - Annapolis/ColumbiaAnnapolis, Maryland$51,545–$88,987 / yearIn collaboration with the physician, reviews patients for changes in condition, adverse events, concomitant medication use, protocol compliance, response to study drug and thoroughly documents all findings and participates in data collection of all subjects. Duties include but not limited to assuring protocol compliance for all patients enrolled in the trial, participation in the informed consent process, perform ongoing assessments and documentation in collaboration with physicians and other providers.
Clinical Research Coordinator II-Rockville/Bethesda Maryland OncologyClinical Research Coordinator II-Rockville/BethesdaRockville, Maryland$58,798–$77,435 / yearPrepares study‑related documentation, including protocol worksheets, adverse event reports, institutional review board (IRB) documents, and annual continuing review reports. Duties include but not limited to assuring protocol compliance for all patients enrolled in the trial, participation in the informed consent process, perform ongoing assessments and documentation in collaboration with physicians and other providers.
NewClinical Research Coordinator Virginia Cancer SpecialistsClinical Research CoordinatorFairfax, VirginiaWorks with team to determine effective strategies for promoting/recruiting research participants and retaining participants in long-term clinical trials. In collaboration with the physician and other providers, reviews patients for changes in condition, adverse events, concomitant medication use, protocol compliance, response to study drug and thoroughly documents all findings.
NewResearch Assistant (Job ID: 2026-3891) The Brookings InstitutionResearch Assistant (Job ID: 2026-3891)Washington, DCThe allocation of duties below describes the average division between tasks; the actual work will vary depending on the project needs of the scholars or centers to whom the Research Assistant is assigned and some assignments emphasize policy research and communications more than quantitative analysis. The Urban-Brookings Tax Policy Center (TPC) aims to provide independent analyses of current and longer-term tax issues and to communicate its analyses to the public and to policymakers in a timely and accessible manner.
NewSenior Research Coordinator - Clinical Trials Unit Kennedy Krieger InstituteSenior Research Coordinator - Clinical Trials UnitBaltimore, MarylandIn addition to operational management of multiple research studies, the Senior Research Coordinator will see patients participating in ongoing clinical trials, and will be responsible for specimen collection, processing, and DOT/ IATA compliant handling and shipment. Such activities include: (1) participant recruitment and scheduling, (2) study procedure scheduling and coordination, (3) conducting patient visits and executing study procedures, (4) managing specimen collection and processing, (5) obtaining results and ensuring clinician review, (6) documentation completion, and (7) reporting.
Research Technician II - Social Science Washington University in St LouisResearch Technician II - Social ScienceWashingtonCommunicate daily with the other members of the lab (graduate students, post-docs, and undergraduate research assistants) to coordinate scheduling and train and work with undergraduates on various aspects of the project. The screenings will include criminal background check and, as applicable for the position, other background checks, drug screen, an employment and education or licensure/certification verification, physical examination, certain vaccinations and/or governmental registry checks.
Research Assistant DetailsResearch AssistantWashington DC, WashingtonThe current focuses in lab include the following directions: 1) Developing computational methods for integrating multi-modal data, such as scRNA-seq, scATAC-seq, spatial transcriptomics, ChIP-seq, and CRISPR screening. The university has a significant presence across Virginia, including the Innovation Campus in Northern Virginia; the Health Sciences and Technology Campus in Roanoke; sites in Newport News and Richmond; and numerous Extension offices and research centers .
Part Time Research Assistant DetailsPart Time Research AssistantWashington DC, WashingtonCurrent projects include functional regulation of chromatin modifying enzymes by novel protein-RNA and protein-protein interactions, how disruption of balancing between heterochromatin and euchromatin contributes to early oncogenesis in pediatric brain cancers, and non-histone targets of histone-modifying enzymes. The university has a significant presence across Virginia, including the Innovation Campus in Northern Virginia; the Health Sciences and Technology Campus in Roanoke; sites in Newport News and Richmond; and numerous Extension offices and research centers .
Lead Research Associate - Clinical Data Manager (REDCap) WestatLead Research Associate - Clinical Data Manager (REDCap)Bethesda, MD$82,000–$109,000 / yearA strong understanding of electronic Case Report Forms (eCRFs), surveys, and clinical databases (EDC, ePRO, eConsent) for clinical trial and clinical intervention study protocols and the ability to work with scientific protocol lead staff and systems developers is required. Any offer of employment may be contingent upon receipt of acceptable results from a post-offer background screening, if required for the specific position, which may include, for example, identity verification, employment history, motor vehicle driving record history, and criminal or sexual offender records history.
Clinical Research Coordinator No-Resistance Consulting GroupClinical Research CoordinatorGreenbelt, MD$22.50–$25 / hourFull timeJob Location:PM Pediatric Urgent Care, Greenbelt Maryland Expected Start Date: OctoberCompany Description:Headquartered in Birmingham, No Resistance is a clinical trial site management organization that performs clinical trials in urgent care centers throughout the north and southeast. Assuring protocol compliance and efficient workflow including organizing clinical work areas, tracking and ordering study supplies and shipping materials, checking and replacing expired items, etc.
Research Assistant: Foreign and Defense Policy; Demographics and Political Economy AEIResearch Assistant: Foreign and Defense Policy; Demographics and Political EconomyWashington, DC$50,000–$54,000 / yearHelp plan, organize, and coordinate major public events and private meetings by inviting speakers, drafting public invitations, preparing materials, and coordinating all logistics with AEI’s Events department and media team. Qualified candidates will have a demonstrated interest in topics pertaining to demographics and international political economy and be well organized, intellectually curious, and strong writers.
Senior Clinical Research Associate IRESenior Clinical Research AssociateWashington DC, District of ColumbiaPerform remote and on-site monitoring/co-monitoring visits (Site Qualification Visits, Site Initiation Visits, Interim Monitoring Visits and Close-Out Visits) to ensure data integrity and subject safety in the client's trials. CRA role will support the client's Oncology clinical trials to ensure data integrity, subject safety, and inspection readiness at the clinical investigative sites.
Part-Time Or Full-Time Physician - Clinical Research Headlands ResearchPart-Time Or Full-Time Physician - Clinical ResearchBaltimore, MDPharmasite Research, located in the greater Baltimore area, is a dedicated clinical research site with over twenty years of experience across multiple therapeutic areas, with a particular focus on mental health and central nervous system (CNS) conditions. With an experienced team serving a diverse population, Pharmasite Research partners with sponsors and CROs to advance innovative therapies and improve health outcomes.
Part-time or Full-time Physician - Clinical Research Headlands ResearchPart-time or Full-time Physician - Clinical ResearchBaltimore, MarylandPharmasite Research, located in the greater Baltimore area, is a dedicated clinical research site with over twenty years of experience across multiple therapeutic areas, with a particular focus on mental health and central nervous system (CNS) conditions. With an experienced team serving a diverse population, Pharmasite Research partners with sponsors and CROs to advance innovative therapies and improve health outcomes.
Clinical Research Coordinator (Prn) Trinity Health CorporationClinical Research Coordinator (Prn)Silver Spring, MD$27.75–$44 / hourHoly Cross Hospital, in Silver Spring, is one of the largest hospitals in Maryland, and Holy Cross Germantown Hospital is the first hospital in the nation built on a community college campus, enhanced by an educational partnership. Position Purpose: The Clinical Research Coordinator coordinates pharmaceutical company, National Cancer Institute (NCI), multisite and in-house protocol activities for the Cancer Program and principal investigators.
Clinical Research Coordinator George Mason UniversityClinical Research CoordinatorFairfax, VirginiaCMI faculty have active collaborations with healthcare institutions including the Walter Reed National Military Medical Center, INOVA, Children's National Medical Center, National Rehabilitation Hospital, government agencies such as the FDA, as well as federal laboratories such as the Naval Research Laboratory, NIH Clinical Center, and a number of academic medical centers in the National Capital Region. Contribute to research with high public health significance, including chronic pain and disability; Work closely with researchers using cutting edge technology, such as ecological momentary assessment, biomechanical assessments, AI and natural language processing, 3D motion capture, and advanced medical imaging; and.
NewClinical Research Coordinator CENTER FOR DERMATOLOGYClinical Research CoordinatorWashington, DCThis paid position offers comprehensive training opportunities and the chance to develop your expertise in clinical research while supporting groundbreaking medical advancements. Oversee clinical laboratory procedures and collaborate with laboratory personnel to ensure accurate sample handling and analysis skills are maintained.
Clinical Research Coordinator III - Cardiology MedStar HealthClinical Research Coordinator III - CardiologyWashington, DC$65,062–$117,291 / yearFull timeSupports an investigator-initiated IND or IDE study; prepares for internal or external audits and/or FDA inspections; assists and facilitates research and/or project team meetings; coordinates multi-center studies as applicable; acts as a liaison for research participants investigators sponsors and healthcare professionals and compose clear precise and detailed correspondence; schedules and leads site qualification study initiation monitoring and close-out visits; Ensures that all key personnel engaged in the research project have met training requirements in accordance with Federal regulations institution and sponsor policies and procedures; maintains effective and ongoing communication with sponsor multidisciplinary ancillary and inter-professional research teams; understands and contributes to scientific center goals and growth and maintains knowledge in the field through attending related project meetings reading related literature and maintains professional associations as appropriate. Works with study team as needed to define biospecimen collection processing and storage procedures; trains others as needed to collect and label samples as instructed and delivers or processes samples in accordance with protocol; communicates with manager investigator and sponsor regarding laboratory findings and recognizes common laboratory values and alerts; maintains current Occupational Safety and Health Administration (OSHA) training regarding Bloodborne Pathogens and International Air Transportation Association (IATA) training for routine packing labeling and transporting of biological materials.