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.
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.
Clinical Research Coordinator I Velocity Clinical Research, Inc.Clinical Research Coordinator ID.C Pediatrics, Washington, DCTemporaryCoordinate, with supervision, assigned clinical trials including start up, vendor management, subject recruitment, source development review, scheduling subjects, protocol training, collection of regulatory documents, conducting visits, ensuring data is entered in a timely manner and all queries are resolved, managing, and reporting adverse events, serious adverse events, and deviations, implementing new protocol amendments, providing all close out reports. Overview: Velocity Clinical Research is an owned and integrated research site organization, providing excellence in patient care, high quality data and fully integrated research sites.
Clinical Research Coordinator - Annapolis Maryland OncologyClinical Research Coordinator - AnnapolisAnnapolis, Maryland$51,545–$88,987 / 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.
Sr. Clinical Research Associate ICON PlcSr. Clinical Research AssociateWashington, WA$110,520–$138,150 / yearWilling and able to travel up to 50% for on-site monitoring visits across the West region; preference given to candidates residing near major HUB airport to support efficient regional travel. ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
Research Coordinator Clinical Trials Unit Kennedy Krieger Institute IncResearch Coordinator Clinical Trials UnitBaltimore, MDUnder the direction of the Senior Research Coordinator, assist and support daily clinical trial and research study activities, including participant recruitment and scheduling, study procedure scheduling and coordination, obtaining results and ensuring clinician review, and documentation completion.3. The Research Coordinator assists and collaborates with the Principal Investigator (PI) and research collaborators for research studies related to neurological, neurogenetic neurodevelopmental and psychiatric conditions in children, adolescents, and adults.
Research Coordinator - Clinical Trials Unit Kennedy Krieger InstituteResearch Coordinator - Clinical Trials UnitBaltimore, MDUnder the direction of the Senior Research Coordinator, assist and support daily clinical trial and research study activities, including participant recruitment and scheduling, study procedure scheduling and coordination, obtaining results and ensuring clinician review, and documentation completion.3. The Research Coordinator assists and collaborates with the Principal Investigator (PI) and research collaborators for research studies related to neurological, neurogenetic neurodevelopmental and psychiatric conditions in children, adolescents, and adults.
Clinical Research Coordinator II - Burn & Surgical Research MedStar HealthClinical Research Coordinator II - Burn & Surgical ResearchWashington, DC$59,820–$101,836 / yearCollaborate across teams: Serve as a liaison among participants, investigators, sponsors, CROs, and healthcare professionals while supporting study monitoring, initiation, and close-out visits. Maintain study data: Complete accurate clinical documentation and case report forms, enter data into the CTMS within required timelines, and resolve data queries with sponsors/CROs.
Clinical Laboratory Scientist, Laboratory Information System (LIS) GuidehouseClinical Laboratory Scientist, Laboratory Information System (LIS)Bethesda, Maryland$85,000–$141,000 / yearAbility to Obtain Public Trust We are currently searching for a Clinical Laboratory Scientist (CLS) with Super User or Administrative experience working with a clinical hospital laboratory information system (LIS) to provide support to the National Institutes of Health (NIH), Department of Laboratory Medicine (DLM). Successful completion of a Medical Laboratory Scientist/Clinical Laboratory Scientist program accredited by the National Accrediting Agency for Clinical Laboratory Sciences (NAACLS) or an accrediting body recognized by the U.S. Department of Education at the time the degree was obtained.
Oncology Clinical Informaticist I Registered Nurse (RN) MedStar HealthOncology Clinical Informaticist I Registered Nurse (RN)Baltimore, MD$82,617.60–$143,062.40 / yearEstablishes develops and maintains effective relationships working agreements and quality partnerships within the shared decision-making model and within the model of care to ensure quality patient care across the continuum and to secure resources to support evidence based patient care. Functions as a facilitator and innovator for state-of-the-art clinical care with direct involvement in implementing and evaluating new techniques and equipment for safety cost-effectiveness and benefits related to clinical practice.
Director, Clinical Practice American Gastroenterological AssociationDirector, Clinical PracticeBethesda, MarylandAMERICAN GASTROENTEROLOGICAL ASSOCIATION INSTITUTE POSITION DESCRIPTION POSITION TITLE: Director, Clinical Practice REPORTS TO: Vice President, Practice and Quality SUMMARY: Support the work of the AGA Institute by overseeing the development and implementation of all components of AGA’s clinical practice documents, tools, programs and special initiatives. This position serves as staff liaison to the Clinical Guidelines Committee and the Clinical Practice Updates Committee to identify current and upcoming clinical issues and trends, and assist AGA staff in the formulation, coordination, and implementation of relevant organizational policies, programs, services and products.
Clinical Research Assistant I - CDP The Henry M Jackson Foundation for the Advancement of Military Medicine IncClinical Research Assistant I - CDPBethesda, MDThe Clinical Research Assistant I will assist with activities related to CDP's mission, which is 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. CDP strives to be the central hub for the Military Health System (MHS) in the development and implementation of training and education to clinicians in order to ensure that all service members, veterans, and their families receive quality behavioral healthcare that meets their unique needs.
Temporary - Clinical Research Coordinator AxleTemporary - Clinical Research CoordinatorBaltimore, MD$60–$64 / hourAssist staff on all facets of clinical studies including subject enrollment, scheduling outpatient appointments and inpatient admissions, travel arrangements, investigation consent, subject longitudinal monitoring, study data, sample collection and data entry. Work products and documents related to data entry in the electronic medical record system., generating reports; perform study procedures; process and destroy specimens as needed; maintain storage records/inventory of biological specimens.
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.
Director Medical Affairs - Clinical Microbiology Waters CorporationDirector Medical Affairs - Clinical MicrobiologyWashington DC, DCThe Director is expected to bring deep diagnostic and laboratory expertise, strong business acumen, and a collaborative leadership style to advance medical credibility, innovation, and patient impact across Waters Advanced Diagnostics. This individual translates unmet customer and patient needs, evolving clinical practice, and real-world evidence into actionable medical strategies that strengthen product differentiation, support lifecycle decisions, and enable successful development and adoption of innovative diagnostic solutions.
Clinical Nurse Specialist - Oncology and Gynecology Research The Henry M Jackson Foundation for the Advancement of Military Medicine IncClinical Nurse Specialist - Oncology and Gynecology ResearchBethesda, MDHJF is seeking a Clinical Nurse Specialist - Oncology and Gynecology Research to support the Gynecologic Cancer Center of Excellence (GYN-COE) at Walter Reed National Military Medical Center (WRNMMC) in Bethesda, Maryland. This role serves as a critical liaison among patients, physicians, research staff, and multidisciplinary care teams to ensure high-quality clinical care and research execution.
Clinical Project Manager – Behavioral Health (LCSW-C Required) Behavioral HealthClinical Project Manager – Behavioral Health (LCSW-C Required)Baltimore, MD$90,000–$125,000 / yearFull timeWe are seeking an LCSW-C Clinical Project Manager to oversee behavioral health plans and provide clinical supervision for direct care staff. This role ensures high-quality trauma-informed services for youth in care.
Research Associate (Per Diem Flex Shift) ParexelResearch Associate (Per Diem Flex Shift)Baltimore, MarylandMinimum availability requirements: 16 hours of availability per week AND two 12-hour weekend shifts in a 4-week month OR three 12-hour weekend shifts in a 5-week month. Recruit study participants by calling the database, attending company sponsored community events, posting flyers in schools, senior centers, supermarkets, and other establishments.
Postdoctoral Research Associate - Oncology Washington University in St LouisPostdoctoral Research Associate - OncologyWashingtonThe Global Oncology Initiative (GOI) within the Division of Oncology at WashU Medicine is seeking a highly motivated Postdoctoral Research Associate to support implementation and clinical research activities across a portfolio of global oncology projects in East Africa. The postdoctoral researcher will receive mentorship and training in study coordination, IRB and regulatory processes, grants management, scientific writing, implementation research methods, and cross-site project management.
Senior Clinical Research Coordinator The Geneva FoundationSenior Clinical Research CoordinatorBethesda, MarylandMaintain and update files of all applicable regulatory documentation for IACUC or IRB (including protocols, approvals, amendments, modifications, etc.) as well as any communications with the sponsor or any other Federal or regulatory office (including prior approvals, change in scope, etc. Coordinate the day-to-day activities of technical support staff specifically engaged in the carrying out of research/clinical protocol, as appropriate to the position; may perform aspects of research protocol, as required, in accordance with specified program objectives.