Research Pharmacy Assistant MedStar HealthResearch Pharmacy AssistantWashington, DC$19.55–$34.25 / hourFull timeAssists in the development of computer programs and other aids to monitor and improve the Research Pharmacy Program and aids other support personnel. Updates and maintains records of the receipt dispensing storage and return or destruction of study related materials in accordance with Federal local and hospital regulations.
Clinical Research Coordinator I - MPS The Henry M Jackson Foundation for the Advancement of Military Medicine IncClinical Research Coordinator I - MPSBethesda, MDThe Clinical Research Coordinator I assists with CDP's research activities in support of their mission to lead the development of a community of military culturally mindful and clinically competent providers through the delivery of high-quality training and education, the convening of experts, and the dissemination of research-based treatment and the latest topics in military behavioral health. Conducts research in collaboration with investigators and other staff to include interaction with study subjects for screening, recruitment and data collection, applying quality control measures as outlined/required by the protocol; contributing to the collection and organization of data; performing basic data entry and coding.
Clinical Research Coordinator GuidehouseClinical Research CoordinatorBethesda, MarylandEnsure study records remain inspection-ready and audit-ready by maintaining regulatory binders, study files, delegation-of-authority logs, and associated study documentation; support audit preparation and inspection readiness activities. Ensure protocol conduct complies with National Cancer Institute (NCI), National Institutes of Health (NIH), Food and Drug Administration (FDA), International Council for Harmonization-Good Clinical Practice (ICH-GCP), and applicable regulatory requirements.
NewClinical Research Supervisor (GU) University of ColoradoClinical Research Supervisor (GU)Washington, DC$67,511–$85,874 / yearJob Summary: As an important member of the research team, the Clinical Research Supervisor will report to the team manager This position works with Phase I-IV industry-sponsored, co-operative group and or investigator-initiated clinical trials in accordance with the trial protocols, FDA Regulations, and ICH/GCP Guidelines. It is accountable for meeting study-specific goals and timelines, while also performing and assisting with clinical tasks related to study-specific tests, procedures, and treatments as assigned based on appropriate licensure and/or completion of competency documentation and team needs.
Clinical Research Coordinator GW- Washington DC Maryland OncologyClinical Research Coordinator GW- Washington DCBeltsville, Maryland$51,545–$88,987 / yearResponsible for supporting the management and coordination of tasks for multiple clinical research studies to include screening patients for eligibility and participates in the subject’s study visits and required activities per protocol. Prepares study‑related documentation, including protocol worksheets, adverse event reports, institutional review board (IRB) documents, and annual continuing review reports.
Research Assistant, Economic Policy Center for American ProgressResearch Assistant, Economic PolicyWashington, DC$55,000–$63,250 / yearAmerican Progress is seeking a Research Assistant on its Economic Policy team to support work on policy topics across American Progress, including those related to affordability, economic mobility, and economic growth in the context of building an economy that works for all. The ideal candidate is a highly organized, detail-oriented, and responsible individual who is intellectually curious and has a strong desire to find answers to challenging research questions as well as the ability to multitask.
NewPart-Time Clinical Research Coordinator Actalent IncPart-Time Clinical Research CoordinatorFalls Church, VA$25–$33 / hourWe are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing winner for both client and talent service. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.
Research Assistant La Clinica Del PuebloResearch AssistantWashington, DCLa Clinica del Pueblo is working with the Department of Epidemiology in the Milken Institute School of Public Health at George Washington University (GWU) to assist the department in conducting an NIH-funded study, the DC Cohort, a longitudinal multi-site study of people with HIV. LCDP is seeking a Research Assistant (RA) to assist in the conduct of this study including assisting with participant recruitment and data capture and assisting the Site Principal Investigator and LCDP research team with the overall implementation, coordination and management.
Senior Clinical Research Associate (level dependent on experience) CTISenior Clinical Research Associate (level dependent on experience)WashingtonFor that reason, we treat our team members with the respect they deserve, and our numbers show it: We support career progression – We believe in promoting from within and we have a structured mentoring program and program for recent graduates to provide the support employees need to move forward. To help support the unique job functions of our CRAs, we have a dedicated training department that offers ongoing therapeutic training sessions from our world-class medical directors, and an experienced and supportive management team that is there to offer continual guidance.
Clinical Research Manager The Geneva FoundationClinical Research ManagerBethesda, MarylandMaintain and update files of all applicable regulatory documentation for IRB (including protocols, approvals, amendments, modifications, etc.) as well as internal study documents (logs, manual of procedures, etc.), and any communications with the sponsor or any other Federal or regulatory office (including prior approvals, change in scope, etc.). Oversee, prepare, and track regulatory lifecycle actions submitted to the Institutional Review Board (IRB) spanning from initial submissions to continuing review submissions, protocol amendments/modifications, reportable events, and closure reports, etc.
Research Assistant, Nuclear Policy Program Carnegie Endowment for International PeaceResearch Assistant, Nuclear Policy ProgramWashington, DC$50,000–$52,000 / yearThe selected candidate will work closely with-and support the research of-NPP's collection of world-leading scholars on topics including deterrence, arms control, nonproliferation, and nuclear energy. The Carnegie Endowment for International Peace, a renowned international affairs institution, seeks a full-time research assistant to support its Washington, DC based Nuclear Policy Program.
Research Assistant, Social, Cultural, and Constitutional Studies (Civic Life and Law) AEIResearch Assistant, Social, Cultural, and Constitutional Studies (Civic Life and Law)Washington, DC$50,000–$54,000 / yearCandidates should have: Previous internship or full-time work experience in research, writing, editing, and quantitative analysis (experience with podcast production is a plus); Strong oral and written communication skills; Excellent organizational skills and the capacity to manage multiple overlapping project timelines; Demonstrated interest in American civil society, philanthropy, family policy, and religious liberty, along with a familiarity with current events; Proficiency in performing administrative and logistical coordination tasks; Attention to detail, demonstrated capacity to work independently, and a high level of initiative; and. Manage logistical and administrative tasks related to scholars’ activities, including scheduling, processing expense reimbursements, posting content on the AEI website, tracking scholar output, and planning and staffing public-facing events and conferences, private meetings, and roundtables.
Research Assistant (Justice Policy Center) Urban InstituteResearch Assistant (Justice Policy Center)Washington, DCWho You Are: The successful candidate will possess: Bachelor's degree or associate's degree with equivalent experience required, preferably in public policy, criminology, sociology, economics, statistics, political science, psychology, public health, data science, or a related field. The Opportunity: The Justice Policy Center (JPC) conducts objective, interdisciplinary research and policy analysis across issues including community safety, policing, courts, corrections, reentry, violence prevention, victimization, youth justice, and system reform.
Research Assistant/Associate Center For A New American Security Inc.Research Assistant/AssociateWashington, DCBuilding on the deep expertise and broad experience of its staff and advisors, CNAS engages policymakers, experts, and the public with innovative fact-based research, ideas, and analysis to shape and elevate the national security debate. EVENT DESIGN AND MANAGEMENT Plan, manage, and execute Defense Program events, including wargames run by The Gaming Lab, private roundtables, and public events.
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.
Clinical Research Coordinator II (Frederick/Germantown) Maryland OncologyClinical Research Coordinator II (Frederick/Germantown)Frederick, Maryland$58,798–$77,435 / 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.
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.
NewNurse (Clinical Research) US Department of Health and Human ServicesNurse (Clinical Research)Washington, DC$85,532–$120,051 / yearIn addition, to qualify for a Nurse (Clinical Research) position at the GS-11 level, you must have at least 1 year of professional Nurse experience equivalent to at least the GS-09 level in the federal service obtained in either the private or public sector, performing the following types of tasks: 1.) Providing comprehensive nursing care to patients based on the physicians medical care plan and the physical, mental and emotional needs of the patient 2.) Administering oxygen, IV fluid, blood transfusions and prescribed oral, subcutaneous and intramuscular medications. This position is designated as an "emergency essential" position and the selected candidate will be considered an "emergency essential" employee and will be required to be available, ready, willing, and able to report for duty under all circumstances (e.g., inclement weather, government closings and holidays, lapses in appropriations, non-emergency and emergency situations) for operation 24 hours a day and 365 days per year coverage.
Clinical Research Coordinator I CenExelClinical Research Coordinator IGaithersburg, MarylandRecently 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.