Clinical Laboratory Technician - Siteman Cancer Center Washington University in St LouisClinical Laboratory Technician - Siteman Cancer CenterWashingtonA successful candidate will have strong clerical accuracy, exceptional organization and time-management skills, a solid understanding of basic computer applications, experience working in a laboratory environment and should be motivated to join a fast-paced laboratory environment. Assay, Clinical Laboratory Operations, Detail-Oriented, Equipment Maintenance, Growth Development, Medical Laboratories, Microsoft Excel, Prioritization, Regulatory Requirements, Task Organization, Team Collaboration, Troubleshooting Grade .
Clinical Trial Participants Needed - Earn Up to $4,000 Part-Time Apex ResearchClinical Trial Participants Needed - Earn Up to $4,000 Part-TimeClinton, MDFull timeTake advantage of this unique opportunity to earn extra income, access quality medical care, and contribute to life-changing research. Most trials don’t require health insurance, so this is your chance to get access to care and gain a better understanding of your condition.
Nuclear Medicine Technologist - Radiology Washington University in St LouisNuclear Medicine Technologist - RadiologyWashingtonPrimary liaison to PI in developing plans for research projects that includes nuclear medicine studies and discussing the interpretation of results; collaborates in the preparation of manuscripts for publication and preparation of grant/trial proposals to sponsoring entities; assists in the preparation of study budgets, amendments to protocols, and/or modifications to study design as appropriate. 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, transfer of data, and maintenance of databases in accordance with research protocols and regulatory procedures.
NewGlobal Clinical Operations Program Director, Late Development Oncology AstraZeneca PlcGlobal Clinical Operations Program Director, Late Development OncologyGaithersburg, MD$203,709.60–$305,564.40 / yearIssue Resolution and Partner Management: Lead large or complex deliverables and proactively identify, solve or escalate operational issues; drive delivery through internal teams and external partners (alliance partners, CROs, vendors and AROs) and act as the AstraZeneca point of escalation for externally managed studies. Cross-Functional Delivery: Lead cross-functional teams in delivery of assigned Clinical Program Team activities; serve as a subject matter expert across functional and cross-functional initiatives.
Associate Director, Clinical Sciences, Oncology ModernaTXAssociate Director, Clinical Sciences, OncologyBethesda, MassachusettsWe are proud to have been recognized as a Science Magazine Top Biopharma Employer, a Fast Company Best Workplace for Innovators, and a Great Place to Work in the U.S. If you want to make a difference and join a team that is changing the future of medicine, we invite you to visit modernatx.com/careers to learn more about our current opportunities. Broadly stated, in conjunction with the Clinical Study Lead and the broader Clinical Trial Team, oversee end-to-end delivery of clinical trial protocols including study design, initiation, medical safety data monitoring, data dissemination and closeout activities.
NewBoard Liaison (Remote) HR Knowledge SourceBoard Liaison (Remote)Alexandria, VARemote$85,000–$90,000One of the first diversity focused organizations in the United States, National Medical Fellowships (NMF), founded in 1946, is the nation's premier 501(c)(3) non-profit organization seeking to eliminate health care disparities by increasing the number of Black, Indigenous, and People of Color (BIPOC) physicians and other health care professions working to advance health equity. NMF works to expand access to education in health care professions, strengthen partnerships with institutions providing this education, and increase a sense of belonging for BIPOC students by enhancing its financial, communal, and emotional support.
Safety & Pharmacovigilance Specialist I Zp Group LlcSafety & Pharmacovigilance Specialist IBethesda, MDSupport clinical research activities for both marketed and investigational drugs, including adverse event reporting and analysis. Qualifications for the Safety & Pharmacovigilance Specialist I include: Familiarity with GCP and ICH guidelines; experience in drug development and clinical trials required.
Central Monitor Zp Group LlcCentral MonitorBethesda, MD$85,000–$125,000 / yearKeywords: Central Monitoring, Risk-Based Quality Management, Clinical Trials, ICH GCP, KRIs, QTLs, Clinical Risk Management, CRO, CRA, Data Analysis, FDA Regulations, Oncology, Infectious Disease, Clinical Research, Remote, Bethesda MD. Excellent facilitation, presentation, and problem-solving skills; strong written and verbal communication; attention to detail and quality control; and experience with clinical research systems and tools.
Mental Health Patient Recruitment Specialist Lead CenExelMental Health Patient Recruitment Specialist LeadGaithersburg, MarylandDoes daily and weekly scheduling of pre-screen appointments for the community outreach team, ensuring appointments are consistently booked and evenly distributed throughout the week. Recently acquired by BayPine Capital Partners, our research sites provide unparalleled medical and scientific support in the design and execution of clinical trials.
NewStudy Coordinator IREStudy CoordinatorUs, WashingtonStudy Coordinator- Bothell, WA ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a Clinical Study Coordinator at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.
NewSafety Committee Specialist, DSMB Digital InfuzionSafety Committee Specialist, DSMBRockville, MDFull timeReporting to the Director of Clinical Research Solutions, this SCS position is ideal for someone who enjoys building structure, thrives in fast-paced environments, and takes pride in ensuring no detail is overlooked in the service of patient safety and research quality. This role will play a critical part in both ensuring regulatory alignment and overseeing the detailed coordination and logistics needed to support DSMB operations for 30 DSMBs within an electronic management system.
Senior Technical Project Manager (Hybrid) - Radiology Washington University in St LouisSenior Technical Project Manager (Hybrid) - RadiologyWashingtonAtlassian Confluence, Atlassian JIRA, Biomedical Informatics, CI/CD, Communication, Cross-Team Coordination, DICOM Images, End User Documentation, GitHub, Git Workflow, Life Sciences Industry, Medical Centers, Medical Imaging, NIH Grants, Open Source Software (OOS), Quality Documentation, Radiology, Release Engineering, Report Writing, Scrum (Agile), Software Development Process, XNAT Grade . TPM will serve as the operational backbone of XNAT — coordinating a distributed team of internal engineers and external open-source contributors, managing release engineering, driving documentation quality, and communicating progress to funders, institutional partners, and the broader imaging informatics community.
RN Clinical Services Group Manager Becton Dickinson and CoRN Clinical Services Group ManagerWashington D.C., DCMaster's Degree in Nursing (MSN), including Advanced Practice Registered Nurse (APRN), Nurse Practitioner (NP), or Physician Assistant (PA) with Critical Care experience in Intensive Care Unit (ICU), Operating Room (OR), Emergency Room (ED) or related field with equivalent to 6 years of experience of previous related experience with direct healthcare management within large clinical organizations preferred. Bachelor's Degree in Nursing (BSN), with Critical Care experience in Intensive Care Unit (ICU), Operating Room (OR), Emergency Room (ED) or related field with 8 years of previous related experience with direct healthcare management within large clinical organizations required.
GMP Project Manager Camris International IncGMP Project ManagerSilver Spring, MDResponsibilities: Manage development and manufacturing program schedules to ensure new projects are kicked off according to schedule, in-progress activities are completed on time, and deliverables are sufficiently high quality. CAMRIS International, LLC, is a dynamic medical research and development firm that achieves innovative solutions to health and development challenges through high-quality, cost-effective programs and research management services.
Sr. Project Manager, CDMO and Facilities Camris International IncSr. Project Manager, CDMO and FacilitiesSilver Spring, MDPlan, 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. Our core practice areas include vaccine research, development, and production; microbiology and infectious disease research; biodefense; clinical research; global health security; and HIV/AIDS programs.
GMP Senior Project Manager Camris International IncGMP Senior Project ManagerSilver Spring, MDPhysical Requirements, Workplace Hazards and Conditions, and PPE and Chemical Requirements: The 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. Overview: We are seeking a GMP Senior Project Manager to support the Pilot Bioproduction Facility (PBF) at the Walter Reed Army Institute of Research (WRAIR) in Silver Spring, Maryland.
Data Analyst Georgetown UniversityData AnalystDC$26.26–$48.32 / hourWith the Hilltop Campus located in the heart of the historic Georgetown neighborhood, and the Capitol Campus, just minutes from the U.S. Capitol and U.S. Supreme Court, Georgetown University offers rigorous academic programs, a global perspective, and unparalleled opportunities to engage with Washington, D.C. Our community is a close-knit group of remarkable individuals driven by intellectual inquiry, a commitment to social justice, and a shared dedication to making a difference in the world. Data Analyst for Infectious Diseases Clinical Trials Unit will work with and assist the Clinical Research Coordinator, Regulatory Specialist, and Clinical Trial Manager by entering data into clinical trial sponsor system, as well as internal software.
Clinical Informatics Arch Epic Children's National HospitalClinical Informatics Arch EpicDC$103,812.80–$173,035.20 / yearProject Management: Strong analytic thinking and problem-solving skills with mastery of project management, capable of handling multiple initiatives simultaneously, including overseeing successful and fast-paced implementations of enterprise software including the electronic health record (EHR). Please note that it is the policy of Children's National Hospital to ensure a "drug-free" work environment: a workplace free from the illegal use, possession or distribution of controlled substances (as defined in the Controlled Substances Act), or the misuse of legal substances, by all staff (management, employees and contractors).
VP/Senior Director, Neurology Regulatory Affairs IQVIAVP/Senior Director, Neurology Regulatory AffairsWashington, District of ColumbiaThe primary roles and responsibilities include managing the development of regulatory submissions, development of overall regulatory strategy, communicating with regulatory bodies and clients, and leading or expanding new therapy ideas, as applicable. Develop and execute regulatory services for client companies, including however not limited to: Regulatory Submissions (e.g., 510(k), IDE, PMA, IND, BLA, & IND, Technical Documentation, STED, CERs).
Legal Counsel, Health Plan, Clinical Contracts and Governance Children's National HospitalLegal Counsel, Health Plan, Clinical Contracts and GovernanceWashington, DC$131,060.80–$218,441.60 / yearPlease note that it is the policy of Children's National Hospital to ensure a "drug-free" work environment: a workplace free from the illegal use, possession or distribution of controlled substances (as defined in the Controlled Substances Act), or the misuse of legal substances, by all staff (management, employees and contractors). Support legal services for enterprise-wide contracting activities including clinical contracts such as provider service agreements, joint ventures, joint operating agreements and management contracts.