Clinical Provider Auditor I - Maryland Behavioral Health Elevance HealthClinical Provider Auditor I - Maryland Behavioral HealthHanover, MD$28.75–$35.94 / hourBorn out of one of the largest healthcare systems organization in the United States, our rich history gives us a unique and valuable perspective on how to solve the most pressing healthcare challenges. We are a Fortune 25 company with a longstanding history in the healthcare industry, looking for leaders at all levels of the organization who are passionate about making an impact on our members and the communities we serve.
NewClinical Research Study Assistant II - Medical Oncology Washington University in St LouisClinical Research Study Assistant II - Medical OncologyWashingtonCollects data from study participants, medical records, interviews, questionnaires, diagnostic tests and other sources; performs basic evaluation and interpretation of collected data and prepares appropriate reports and documentation as necessary; prepares and distributes study packets and information. Performs basic/scripted assessments to confirm eligibility to participate in study; explains and schedules laboratory and diagnostic procedures and/or treatment as required in the study; refers participants to basic resources as necessary.
Clinical Research Study Assistant II - Obstetrics and Gynecology Washington University in St LouisClinical Research Study Assistant II - Obstetrics and GynecologyWashingtonCollects data from study participants, medical records, interviews, questionnaires, diagnostic tests and other sources; performs basic evaluation and interpretation of collected data and prepares appropriate reports and documentation as necessary; prepares and distributes study packets and information. Performs basic/scripted assessments to confirm eligibility to participate in study; explains and schedules laboratory and diagnostic procedures and/or treatment as required in the study; refers participants to basic resources as necessary.
Clinical Research Study Assistant II (PRN) - Cardiology Washington University in St LouisClinical Research Study Assistant II (PRN) - CardiologyWashingtonCollects data from study participants, medical records, interviews, questionnaires, diagnostic tests and other sources; performs basic evaluation and interpretation of collected data and prepares appropriate reports and documentation as necessary; prepares and distributes study packets and information. Performs assessments; explains and schedules laboratory and diagnostic procedures and/or treatment as required in the study; refers participants to basic resources as necessary.
Clinical Research Study Assistant II - Radiology Washington University in St LouisClinical Research Study Assistant II - RadiologyWashingtonCollects data from study participants, medical records, interviews, questionnaires, diagnostic tests and other sources; performs basic evaluation and interpretation of collected data and prepares appropriate reports and documentation as necessary; prepares and distributes study packets and information. Performs basic/scripted assessments to confirm eligibility to participate in study; explains and schedules laboratory and diagnostic procedures and/or treatment as required in the study; refers participants to basic resources as necessary.
Clinical Research Study Assistant II - Emergency Medicine Washington University in St LouisClinical Research Study Assistant II - Emergency MedicineWashingtonCollects data from study participants, medical records, interviews, questionnaires, diagnostic tests and other sources; performs basic evaluation and interpretation of collected data and prepares appropriate reports and documentation as necessary; prepares and distributes study packets and information. Performs basic/scripted assessments to confirm eligibility to participate in study; explains and schedules laboratory and diagnostic procedures and/or treatment as required in the study; refers participants to basic resources as necessary.
NewRN Clinical Nurse Coordinator II - Pediatric Endocrinology Washington University in St LouisRN Clinical Nurse Coordinator II - Pediatric EndocrinologyWashingtonClinical Knowledge, Clinical Research Coordination, Database Management, Effective Written Communication, Electronic Medical Records (EMR), Emergency Situations, Epic EHR, Family Support, General Nursing, Infection Control Nursing, Interpersonal Communication, Onboarding, Oral Communications, Patient Care Plans, Patient Education, Research Development, Research Methodologies, Safety Practices, Spreadsheets, Statistical Analysis Software (SAS), Team Leadership, Work Collaboratively Grade . Basic Life Support - American Heart Association, Basic Life Support - American Red Cross, Registered Nurse - Illinois Department of Financial and Professional Regulation, Registered Nurse - Missouri Division of Professional Registration.
Clinical Research Coordinator I - Bilingual (Spanish) ObjectiveHealth IncClinical Research Coordinator I - Bilingual (Spanish)Laurel, MDNot easily distracted: You have the ability to stay focused while running different protocols, resolving and submitting IRB responses and audit findings, tracking AE and SAE events, and maintaining eSource material for assigned studies. ObjectiveHealth is a clinical research company that uses proprietary technology to: Increase patient access to research trials within our communities, Provide physicians with enhanced care options for current patients, and.
Clinical Pharmacy Operations Manager ALFA PharmacyClinical Pharmacy Operations ManagerColumbia, MarylandAbout ALFA ALFA Specialty Pharmacy is a pharmacist-led, closed-door pharmacy serving patients with chronic conditions, group homes, intellectual and developmental disabilities (IDD), and long-term care-at-home populations. At ALFA Specialty Pharmacy, pharmacists are essential members of the healthcare team who deliver personalized, high-touch medication management and collaborate with physicians, nurses, caregivers, and families to improve outcomes.
Clinical Research Coordinator I/Ii/Iii Opportunities - Multiple Locations Nationwide Headlands ResearchClinical Research Coordinator I/Ii/Iii Opportunities - Multiple Locations NationwideBaltimore, MD$45,000–$100,000 / yearThis general interest posting is designed for experienced Clinical Research Coordinators (CRCs) who may not see a current opening that aligns with their location, but want to be considered for future opportunities across our growing network of clinical research sites nationwide. They play a hands-on role in advancing new therapies, supporting patients through clinical trials, and ensuring studies are conducted with the highest level of quality and care.
Health Physicist Assistant, Clinical - Radiation Safety Washington University in St LouisHealth Physicist Assistant, Clinical - Radiation SafetyWashingtonExamples of some technical areas include: user authorizations, medical use (clinical and research, nuclear medicine, interventional radiology, radiation oncology), research use (animal, human, in vitro, biological, chemical, physical, engineering), inspections, surveys, cyclotron produced materials (production, distribution, use), imaging, x-ray and fluoroscopy, sealed sources and irradiators, instrument calibration, radioactive materials accountability and transportation (ordering, receipt and distribution), user and staff training, radioactive waste management and shipping (collection, processing, disposal), dosimetry and bioassay, ALARA program, decommissioning, release surveys and closeouts, and emergency response. This position is responsible for assisting health physics staff on assignments for the Washington University and Washington University School of Medicine (WU&WUSM) radiation safety program and for other contracted organizations within and affiliated with the Washington University School of Medicine.
Clinical Research Associate (All levels) - South East, USA Evestia ClinicalClinical Research Associate (All levels) - South East, USAWashington State, WashingtonEvestia Clinical is looking Clinical Research Associate (II or Senior) in the North West to be responsible for ensuring that the rights and safety of clinical trial participants are protected and that the clinical data obtained are accurate, complete, and verifiable according to source. We partner with clients to provide expert guidance through complex clinical trials in specialized areas, including Rare Disease, Oncology, Neurology, and Immunology.
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.
Clinical Research Coordinator GuidehouseClinical Research CoordinatorBethesda, Maryland$65,000–$108,000 / yearAbility to Obtain Public Trust What You Will Do : We are seeking a Clinical Research Coordinator to provide comprehensive clinical research coordination services for oncology and cancer-related clinical trials conducted within the National Cancer Institute (NCI). Ensure 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.
NewResearch Coordinator - Clinical Trials Unit Kennedy Krieger InstituteResearch Coordinator - Clinical Trials UnitBaltimore, Maryland2. Under 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. Overview: 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.
Senior 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.
NewResearch 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.
Senior Research Coordinator Clinical Trials Unit Kennedy Krieger Institute IncSenior Research Coordinator Clinical Trials UnitBaltimore, MDIn 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.5.
NewClinical Research Associate Tenacity Solutions LLCClinical Research AssociateNorth Bethesda, MDJob Description Tenacity Solutions, LLC (Tenacity) is seeking an experienced Clinical Research Quality Associate (CRQA) to support the Department of Veterans Affairs (VA) Cooperative Studies Program (CSP) Site Monitoring, Auditing and Resource Team (SMART). The successful candidate will conduct on-site and remote monitoring visits, assess protocol compliance, review informed consent and regulatory documentation, verify source data, identify compliance issues, support corrective and preventive actions (CAPAs), and prepare comprehensive monitoring reports.
Clinical Research Coordinator II - Pediatrics Gastroenterology Washington University in St LouisClinical Research Coordinator II - Pediatrics GastroenterologyWashingtonImplements and manages all phases of study/protocol; ensures compliance with protocol guidelines and requirements of regulatory agencies; establishes record-keeping systems; makes assessments and determinations of participants’ progress in the study; analyzes, investigates and reports adverse events; makes decisions as when to notify physicians of issues, when to stop participant inclusion and/or to make and/or recommend adjustment of the protocol of particular participants; resolves protocol management issues and recommends corrective action as appropriate; serves as liaison with funding or sponsoring agency. You will work closely with other team members and healthcare professionals to recruit and enroll study participants, explain the purpose of study and obtain informed consent from participants, conduct study visits in the hospital and the participant’s home, ensure compliance with protocol guidelines and requirements of the IRB and IACUC, enter data, assist with lab procedures, and perform data analyses.