NewClinical Research Nurse- Clinical Trails Hurwitz Frederick Health Hospital, Inc.Clinical Research Nurse- Clinical Trails HurwitzFrederick, MD$70,033.60–$103,542.40 / yearPart timeUnder 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).
Clinical Admissions Therapist Maryland Charlie Health IncClinical Admissions Therapist MarylandMD$60,000–$75,000 / yearFurther, base pay is only part of the total compensation package, which, depending on the position, may also include incentive compensation, discretionary bonuses, other short and long-term incentive packages, and other Charlie Health-sponsored benefits.#li-remote #CharlieHealthisHiring. The Clinical Admissions Therapist will be responsible for meeting with clients upon admission, building rapport, completing biopsychosocial assessments, and establishing treatment needs.
Clinical Trial Manager, Clinical Operations, Infectious Disease ModernaTXClinical Trial Manager, Clinical Operations, Infectious DiseaseBethesda, 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. Since our founding in 2010, we have aspired to build the leading mRNA technology platform, the infrastructure to reimagine how medicines are created and delivered, and a world-class team.
Externally Sponsored Research Manager AstraZeneca PlcExternally Sponsored Research ManagerGaithersburg, MD$112,154–$168,232 / yearYou will partner cross‑functionally to lead end‑to‑end start‑up and execution with franchise teams and sites: triaging proposals, coordinating governance, guiding ESR processes, and ensuring contracts, budgets, and systems are accurate and current. As an ESR Manager, you will serve as the operational backbone for externally sponsored research performed in the USA, aligning to franchise priorities to deliver high‑quality, compliant studies that inform practice and broaden patient impact.
Clinical Research Assistant Prism Vision GroupClinical Research AssistantFairfax, Virginia$22.44–$46.62 / hourThe Clinical Research Assistant reports to the RGW Office Manager and RGW Research Lead and will aid in the coordination and conduct of research under the supervision of a designated physician. The Clinical Research Assistant will develop knowledge of the research studies, rationale, subjects and procedures associated with the studies as designated by the Senior/Lead Clinical Research Coordinator.
Adjunct - Clinical Instructor Hood College of Frederick, MDAdjunct - Clinical InstructorFrederick, MDClinical instructors must hold an active Registered Nurse (R.N.) license in the State of Maryland, possess at least two years of recent clinical experience in the relevant specialty area, and have a minimum of a Bachelor of Science in Nursing (BSN); a Master of Science in Nursing (MSN) is preferred. Possess leadership qualities, be organized, able to deal appropriately with delicate situations, and able to effectively communicate and negotiate resolutions with faculty, students, and facility staff regarding problems in the clinical setting.
Clinical Research Coordinator III - Cardiology MedStar Health Research InstituteClinical Research Coordinator III - CardiologyWashington, DC$65,062–$117,291 / yearSupports an investigator-initiated IND or IDE study; prepares for internal or external audits and/or FDA inspections; assists and facilitates research and/or project team meetings; coordinates multi-center studies as applicable; acts as a liaison for research participants investigators sponsors and healthcare professionals and compose clear precise and detailed correspondence; schedules and leads site qualification study initiation monitoring and close-out visits; Ensures that all key personnel engaged in the research project have met training requirements in accordance with Federal regulations institution and sponsor policies and procedures; maintains effective and ongoing communication with sponsor multidisciplinary ancillary and inter-professional research teams; understands and contributes to scientific center goals and growth and maintains knowledge in the field through attending related project meetings reading related literature and maintains professional associations as appropriate. Works with study team as needed to define biospecimen collection processing and storage procedures; trains others as needed to collect and label samples as instructed and delivers or processes samples in accordance with protocol; communicates with manager investigator and sponsor regarding laboratory findings and recognizes common laboratory values and alerts; maintains current Occupational Safety and Health Administration (OSHA) training regarding Bloodborne Pathogens and International Air Transportation Association (IATA) training for routine packing labeling and transporting of biological materials.
Shift Lead XpresSpa.comShift LeadVAThe Shift Lead is responsible for maintaining operational efficiency, ensuring compliance with program protocols, supporting passenger engagement efforts, monitoring workflow, and serving as the primary point of contact for escalations during their shift. The Shift Lead serves as the frontline operational leader during assigned shifts, ensuring smooth day-to-day execution of station activities and supporting the project in achieving operational goals.
Clinical Program Manager (52096) Gap Solutions, Inc.Clinical Program Manager (52096)Bethesda, MDThe Clinical Program Manager shall provide personnel capable of supporting complex clinical research portfolios and ensuring efficient coordination among investigators, research teams, oversight offices, regulatory agencies, collaborating institutions, and other stakeholders involved in the conduct of clinical research. Monitor and coordinate activities associated with: Protocol development; Protocol amendments; Institutional Review Board (IRB) submissions; Regulatory submissions; Continuing reviews; Study activation activities; Clinical trial monitoring activities.
Director, Regulatory Affairs – Regenerative Medicine & Biologics Quality IQVIADirector, Regulatory Affairs – Regenerative Medicine & Biologics QualityWashington, District of ColumbiaExperience: Minimum five years of experience in Regulatory Affairs related to FDA oversight of various human medical products (HCT/Ps, drugs and/or biologics, medical devices, and combination products)developing regulatory deliverables and submissions. The 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.
NewSr. Manager, MedTech Clinical Operations IQVIASr. Manager, MedTech Clinical OperationsWashington, District of ColumbiaIQVIA MedTech is seeking an experienced Clin Ops leader to manage a team of clinical staff working in support of clinical studies to ensure projects are appropriately resourced and employees are trained and meeting project objectives. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.
NewSr Sample Management Specialist Precision Medicine Group LLCSr Sample Management SpecialistFrederick, MD$68,700–$90,000 / yearDevelop project specific sample logistics plans and monitor end-to-end sample activities for each study - site activation and kit supply, patient visit, sample collection, courier pickup & transit monitoring, sample receipt & accessioning, discrepancy management, inventory reconciliation, sample pulls for testing/destruction/shipments. This role is responsible for the coordination, monitoring, and delivery oversight of sample lifecycle activities, including site shipment tracking, accessioning, storage, inventory management, retrieval, shipment coordination, discrepancy resolution, and client reporting for sample management activities.
NewResearch Study Coordinator- Clinical Trails Hurwitz Frederick Health Hospital, Inc.Research Study Coordinator- Clinical Trails HurwitzFrederick, MD$60,028.80–$85,737.60 / yearPart timeMaintains detailed knowledge of all active clinical trials studies and coordinates workflows and processes that provide effective patient management. Able to maintain a high level of confidentiality related to employee and patient information Able to assess and care for patients with special needs with respect to cultural, ethical, and religious differences and physical abilities.
Senior Statistical Project Leader SanofiSenior Statistical Project LeaderWashington, DC$178,500–$257,833.33 / yearAbout the Job: Our Evidence Generation and Decision Science (EGDS) group at Sanofi unites Biostatistics, Clinical Statistical Modeling, and Real-World Evidence to revolutionize data-driven decision making through cutting-edge quantitative science and deliver unparalleled integrated evidence that drives innovation and scientific breakthroughs. Provide advanced level of statistical and scientific contributions to clinical development plans, protocol, SAP, CSR, regulatory documents, studies and submissions activities (when applicable), and provide strategic statistical leadership for responsible projects in Sanofi's solid tumor pipeline.
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.
Medical Lead - Acute Lymphoblastic Leukemia (ALL) AstraZeneca PlcMedical Lead - Acute Lymphoblastic Leukemia (ALL)Gaithersburg, MD$193,281.60–$289,922.40 / yearYou will also provide medical input into the safety profile of the product in collaboration with Patient Safety (PS) physicians and collaborate with the Medical Science Liaisons and work closely with National Clinical Account Managers to appropriately support key accounts. Accountabilities: As the Medical Lead, you will be responsible for leading Medical Affairs activities in Hematology Oncology Franchise and providing medical leadership to the Core Medical Team (CMT).
NewSr. Clinical Project Manager-MedTech IQVIASr. Clinical Project Manager-MedTechWashington, District of ColumbiaThe Senior Clinical Project Manager-MedTech is responsible for leading the planning, execution, and delivery of global MedTech clinical studies supporting the development and commercialization of medical devices. The Senior Clinical Project Manager-MedTech provides strategic leadership across multi-country clinical programs, driving operational excellence, customer satisfaction, and successful study outcomes.
Executive Director, Research & Development Quality Assurance (RDQA) ModernaTXExecutive Director, Research & Development Quality Assurance (RDQA)Bethesda, Massachusetts10+ years’ experience leading multifunctional quality organizations within the research and development sector, with proven excellence across all facets of quality management including experience developing and managing budgets and ensuring efficient allocation of resources to support both short-term initiatives and long-term organizational goals. We 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.
RN Clinical Research – PRN Act for HealthRN Clinical Research – PRNClifton, VirginiaWe are looking for CMRNs to visit an Adult population who can perform the following skills during a mobile visit: Blood specimen collection and processing (nurse will pick up dry ice prior to the visit and drop off at UPS after the visit). Two (2) years' experience in starting and performing Phlebotomy/Peripheral Blood Draw, IVs, and Subcutaneous Injections (date of last practice within 6 months, preferred).
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.