Clinical Trials Program Monitor and Auditor GuidehouseClinical Trials Program Monitor and AuditorBethesda, Maryland$130,000–$216,000 / yearAbility to Obtain Public Trust What You Will Do : We are currently searching for a Clinical Trials Program Monitor and Auditor to independently provide support services to satisfy the overall operational and clinical trial objectives of the National Institute of Allergy and Infectious Diseases (NIAID).This is a full-time, on-site opportunity in Bethesda, MD. Review, coordinate, and contribute to protocol documents and required reports, including study protocols, consent forms, serious adverse event (SAE) reports, project and protocol deviation reports, accrual, and other study status or study website reports.
NewClinical Trials Program Monitor And Auditor GuidehouseClinical Trials Program Monitor And AuditorBethesda, MD$130,000–$216,000 / yearReview, coordinate, and contribute to protocol documents and required reports, including study protocols, consent forms, serious adverse event (SAE) reports, project and protocol deviation reports, accrual, and other study status or study website reports. Review monitoring and audit reports for ongoing studies, resolve monitoring/audit findings by identifying necessary corrective actions and preventive measures; advise sites on the implementation of corrective actions and preventive measures.
Director of Clinical Services - IN PERSON ONLY K&I HEALTHCARE SERVICES LLCDirector of Clinical Services - IN PERSON ONLYBaltimore, MD$90,000–$115,000 / yearFull timePosition Purpose: The Director of Clinical Services is responsible for overseeing the clinical operations of the Outpatient Mental Health Clinic at K&I Healthcare Services, Psychiatric Rehabilitation Program (PRP), Supported Employment Program (SEP), and Outpatient Services (OP). Under the supervision of the CEO/ Executive Director, the Director of Clinical Services is responsible for the following: Provide overall clinical leadership and oversight of OMHC, PRP, SEP, and outpatient therapy services.
Sr. Project Manager, CDMO and Facilities CAMRISSr. Project Manager, CDMO and FacilitiesSilver Spring, MDFull timeShutdown Planning, IT Infrastructure and Facility Project ManagementStakeholder engagement with partner WRAIR leadership branches and contracts coordinating their support for PBF assetsPlan, coordinate, and execute planned facility shutdowns with minimal disruption to manufacturing schedules and regulatory compliance; develop shutdown plans including scope, resource allocation, risk assessments, and recovery protocols. Experience with cybersecurity ATO requirements and Risk Management Framework (RMF).Physical Requirements, Workplace Hazards and Conditions, and PPE and Chemical RequirementsThe physical requirements, workplace hazards and conditions, and PPE and chemical requirements described here are representative of those that a candidate must meet to perform the essential functions of this job.
NewRN Case Manager Transitional Care MedStar Health Research InstituteRN Case Manager Transitional CareBaltimore, MD$89,065–$162,801 / yearManages patient care according to clinical pathways and/or multidisciplinary plan of care and/or management care contracts by directing decision making and identifying and managing barriers that impact on patient care outcomes. Maintains knowledge of regulatory agencies' requirements for discharge planning necessary criteria for admission to various care settings and Medicare's/Medicaid's reimbursement methods for different levels of care.
Clinical Staff Pharmacist - Per Diem Howard University HospitalClinical Staff Pharmacist - Per DiemWashington, DCDepartment Inpatient Pharmacy (Pharmacy Services Division) Reports To Director, Pharmacy Employment Type Per Diem Schedule Per diem, variable; availability for days, evenings, nights, weekends and holidays as needed PAY. In this role you will provide direct pharmaceutical care to patients of all ages — reviewing and interpreting medication orders, evaluating drug therapy against age, organ function and underlying disease, and serving as a drug information resource for clinicians across the Hospital.
NewSenior Director, Competitive Intelligence, Oncology R&D AstraZeneca PlcSenior Director, Competitive Intelligence, Oncology R&DGaithersburg, MD$218,330–$327,494 / yearAs a Senior Director, Competitive Intelligence, you will work with a team of specialists and own the delivery of competitive analysis, using your knowledge of the Oncology therapy area and external resources to shape future-proofed therapy area (TA) strategies. Collaboration and Leadership: Experienced in leading cross-functional teams with ability to influence without authority to lead in a fast-paced, highly matrixed work environment.
NewInfusion Nurse - Fairfax, VA - On-site IQVIAInfusion Nurse - Fairfax, VA - On-siteFairfax, VirginiaIdentifies patients who require increased nursing assessment and management in addition to the clinical trial requirements and collaborate with other members of the healthcare team to ensure patient safety. Performs study-required procedures such as routine lab collection, study-specific sample collection, vital signs, and ECGs, according to the protocol-defined timeline.
Research Project Interviewer - Baltimore - PT SagoResearch Project Interviewer - Baltimore - PTBaltimore, MDThe Research Project Interviewer (RPI) plays a critical role in the successful execution of research studies by supporting subject recruitment, informed consent, study visits, investigational product handling, and study documentation. Collaborate effectively with monitors, the Clinical Project Management team, and site staff to support overall study success.
NewClinical Nurse - Float Kaiser PermanenteClinical Nurse - FloatHalethorpe, MDRemains flexible to changing systems; is expected to demonstrate quality and effectiveness in work habits and clinical practice; and treats co-workers, patients, families, and all members of the health care team with dignity and respect. Coordinates, implements, and evaluates patient teaching plans for area of diabetes mellitus, hypertension, anticoagulant therapy, therapeutic diet instructions, weight control, and other areas as designated.
NewAdvanced Practice Provider (CNS) Clinical Nurse Specialist Pediatrics UVA HealthAdvanced Practice Provider (CNS) Clinical Nurse Specialist PediatricsWASHINGTON, DCUVA Health is an integrated health system with a world-class academic medical center that includes a level 1 trauma center, a level IV NICU, the first NCI-designated Comprehensive Cancer Center in Virginia, and UVA Health Children's, the #1 pediatric hospital in Virginia. UVA Health consists of UVA Health University Medical Center, UVA School of Medicine, UVA School of Nursing, UVA Claude Moore Health Sciences Library, UVA Community Health, and UVA Physicians Group.
NewTravel Licensed Clinical Social Worker (LCSW) - $35 to $40 per hour in Bethesda, MD 22nd Century Healthcare, Inc.Travel Licensed Clinical Social Worker (LCSW) - $35 to $40 per hour in Bethesda, MDBethesda, MD$35–$40Strong diagnostic and clinical skills, professional knowledge of and specialized experience in the theories, ethical principles and practices of clinical social work including family systems therapy, crisis intervention, psychodynamic, and cognitive behavioral interventions to diagnose and treat patients. Determine additional concrete needs for assistance and services in addition to those from which the research participant/family was referred, including housing, food, transportation, vocational support, financial assistance and healthcare resources.
NewClinical Research Nurse- Clinical Trails Hurwitz Frederick Health Hospital IncClinical Research Nurse- Clinical Trails HurwitzFrederick, MD$70,033.60–$103,542.40 / yearUnder the direction of the Principal Investigator (PI), within the scope of nursing practice, and with minimal supervision, assesses, plans, and implements the safe and effective nursing care to Clinical Trials participants from pre-screening through study exit. Must demonstrate and maintain current knowledge and skills in providing appropriate care/contact for patients in the following age groups: X Adolescent (13 years thru 17 years).
NewClinical Research Nurse- Clinical Trails Hurwitz Frederick Memorial Healthcare SystemClinical Research Nurse- Clinical Trails HurwitzFrederick, MD$70,033.60–$103,542.40 / yearUnder the direction of the Principal Investigator (PI), within the scope of nursing practice, and with minimal supervision, assesses, plans, and implements the safe and effective nursing care to Clinical Trials participants from pre-screening through study exit. Must demonstrate and maintain current knowledge and skills in providing appropriate care/contact for patients in the following age groups: X Adolescent (13 years thru 17 years).
Manager Division Clinical Research - Medical Oncology Washington University in St LouisManager Division Clinical Research - Medical OncologyWashingtonAcademic Programs, Accounting, Business Administration, Clinical Research Coordination, Clinical Research Methods, Compliance Requirements, Employee Management, FDA Compliance, FDA Regulations, Financial Resources Management, Grant Funding, Health Care, Institutional Review Board (IRB), Leadership, Oral Communications, Problem Solving, Project Planning, Regulatory Compliance, State Regulations, Written Communication Grade . Responsible for overall clinical research study planning, coordinating, and execution of all study-related activities, including extensive interaction wth the Internal Review Board (IRB), study sponsors, and investigators.
Clinical Research Project Manager II - Cardiology Washington University in St LouisClinical Research Project Manager II - CardiologyWashingtonMaintains current knowledge of evolving domestic and international clinical research regulations and guidance documents, and applicable state and local requirements; proactively conducts gap analyses to assess the impact of regulatory changes on the assigned studies and the broader research program; develops, implements, and monitors corrective systems, updated SOPs, and training initiatives to close identified gaps and ensure sustained compliance across all sites and functional teams. Demonstrates working knowledge of international clinical research regulations and guidelines applicable to assigned studies, and other country-specific requirements; advises study teams on when and how international requirements apply – particularly in multi-national trials or studies with international data transfer, biologics, or device components – and coordinates with regulators affairs and legal counsel as needed to ensure compliant study conduct across all applicable jurisdictions.
NewAssistant Manager Clinical Research (Hybrid) - Radiology Washington University in St LouisAssistant Manager Clinical Research (Hybrid) - RadiologyWashingtonThe 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. Wellness challenges, annual health screenings, mental health resources, mindfulness programs and courses, employee assistance program (EAP), financial resources, access to dietitians, and more!
Clinical Psychologist (Clinical Support Tools) SME IV Knowesis, Inc.Clinical Psychologist (Clinical Support Tools) SME IVSilver Spring, MD$130,000–$176,000 / yearThis role is crucial for promoting the uptake of evidence-based care across the Military Health System (MHS) by developing products tailored to providers, patients, and family members. Manage the full cycle of product development for deliverables targeting healthcare providers, patients, family members, and other MHS stakeholders.
Clinical Research Coordinator III - Pediatrics Gastroenterology Washington University in St LouisClinical Research Coordinator III - Pediatrics GastroenterologyWashingtonYou 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. Serves as responsible for the development of forms, questionnaires and the application of research techniques; assists in writing instructional procedure manuals for study progress, data collection and coding; reviews journals, abstracts and scientific literature to keep abreast of new developments and to obtain information regarding previous studies to aid in the planning of new studies.
Regional Manager, Clinical Research (32366) GI AllianceRegional Manager, Clinical Research (32366)Alexandria, VAPOSITION SUMMARY: The Regional Clinical Research Manager is responsible for the coordination and administration of clinical trials at 3-4 clinical research site locations within a designated region under the direction of the VP of Operations and Director of Research Strategy and Operations. Responsible for maintenance of accurate and complete documentation, primarily executed by the CRCs, including but not limited to regulatory documents, signed informed consent forms, source documentation, drug dispensing logs, subject logs, and study-related communications.