Clinical Research Coordinator III - Pediatrics Gastroenterology Washington University in St LouisClinical Research Coordinator III - Pediatrics GastroenterologySt. Louis, MO$58,300–$90,400 / yearYou 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.
Bilingual Clinical Research Assistant Doctrials LLCBilingual Clinical Research AssistantPhoenix, AZDocTrials was founded with the primary goal of connecting patients and physicians with clinical trials across the US; aiding in the process to discover new therapies, bring hope, and find new treatment for disease. Patient acquisition: You will be responsible for reviewing patient charts for enrolling trials, creating telephone screening sheets, and conducting recruitment calls.
Clinical Research Assistant Doctrials LLCClinical Research AssistantPhoenix, AZDocTrials was founded with the primary goal of connecting patients and physicians with clinical trials across the US; aiding in the process to discover new therapies, bring hope, and find new treatment for disease. Patient acquisition: You will be responsible for reviewing patient charts for enrolling trials, creating telephone screening sheets, and conducting recruitment calls.
Commercial Construction Project Manager Bracane CompanyCommercial Construction Project ManagerDallas, TexasThis is an excellent opportunity for a Project Manager who enjoys leading projects from award through closeout while partnering closely with Superintendents, Project Coordinators, clients, architects, and subcontractors to deliver exceptional results. While our roots are deeply planted in clinical research and addressing health disparities, our global capabilities have expanded to deliver comprehensive operational support, compliance, and innovative solutions across federal, local government, and private sectors.
NewProject Coordinator (LCSW/LCPC) - Crisis Response Carle HealthProject Coordinator (LCSW/LCPC) - Crisis ResponsePekin, IL$26.34–$43.99 / hourLicensed Clinical Social Worker (LCSW) - Illinois Department of Financial and Professional Regulation (IDFPR); Licensed Clinical Psychologist - Illinois Department of Financial and Professional Regulation (IDFPR); Licensed Clinical Professional (LCPC) - Illinois Department of Financial and Professional Regulation (IDFPR); Driver's License - Illinois Secretary of State (ILSOS); Must have control over personal use of all mood-altering chemicals and behaviors. Actively maintains open communication & demonstrates a cooperative, teamwork style with patients, families, other staff members, other healthcare workers, medical staff and community.
Senior Manager, Clinical Product Supply Quality Assurance AbbVie, IncSenior Manager, Clinical Product Supply Quality AssuranceNorth Chicago, ILLead the identification, assessment, and mitigation of quality and supply risks across the product lifecycle, including risks associated with drug substance, drug product, analytical testing, manufacturing, packaging, release, distribution, and clinical supply continuity. Provide oversight and direction for complex investigations, exception reports, deviations, and product quality actions, including high-impact issues affecting multiple functions, sites, products, or clinical programs.
Clinical Study Associate Manager Regeneron Pharmaceuticals IncClinical Study Associate ManagerArmonk, NY$109,900–$179,300 / yearManages aspects of study close-out activities including database lock, reconciliation of vendor contract, study budget, TMF and study drug accountability, may mentor clinical trial management staff, and may be assigned unmasked tasks for studies (e.g., unmasked TMF management, unmasked data review, IVRS point of contact). In this role, you will support the Clinical Study Lead by taking responsibility for areas of clinical trial delivery, applying to both internally sourced studies and studies out-sourced to CROs, while collaborating with the study team internally and externally with vendors such as CROs.
Clinical Data Manager Agilent Technologies IncClinical Data ManagerCA$105,280–$197,400 / yearServe as a subject matter expert (SME) representing Agilent externally and OCMO internally, collaborating with cross-functional teams (Clinical Development, Clinical Operations, CROs, Pharmaceutical Partners, Biostatistics, Quality Affairs/Design Assurance, and Regulatory Affairs) to align on data-related activities and ensure accurate, compliant, and timely data transfers. Responsibilities include but are not limited to: Lead end-to-end clinical data management activities for companion diagnostic studies, including data acquisition, database design, data review, external data integration, reconciliation, quality control, database lock, and preparation of submission-ready datasets supporting global regulatory submissions.
Senior Manager Clinical Product Supply Quality Assurance AbbVie IncSenior Manager Clinical Product Supply Quality AssuranceNorth Chicago, ILLead the identification, assessment, and mitigation of quality and supply risks across the product lifecycle, including risks associated with drug substance, drug product, analytical testing, manufacturing, packaging, release, distribution, and clinical supply continuity. Provide oversight and direction for complex investigations, exception reports, deviations, and product quality actions, including high-impact issues affecting multiple functions, sites, products, or clinical programs.
Clinical Nutrition Manager 3 Sodexo SAClinical Nutrition Manager 3TURLOCK, CA$81,685–$105,710 / yearSodexo is seeking a Registered Dietitian for a full-time Clinical Nutrition Manager position at Covenant Living of Turlock a 51-bed upscale skilled nursing facility in Turlock, CA. Lead daily clinical nutrition operations for a large account, system, or multiple contracts, overseeing both non-exempt and entry-level professional staff.
Medical Director Oncology Clinical Research Hematology & Oncology Physician Starling OncologyMedical Director Oncology Clinical Research Hematology & Oncology PhysicianLas Vegas, NVWorking closely with Starling Oncology's Chief Medical Officer, physicians, clinical research coordinators, and research operations teams, the Medical Director will provide physician leadership for our clinical research program, expand patient access to clinical trials, strengthen Principal Investigator oversight, and help identify the trials that can have the greatest impact for the communities we serve. Formerly known as The Oncology Institute, Starling Oncology offers cutting-edge, evidence-based cancer care to a population of approximately 2.1 million patients, including clinical trials, transfusions, and other care delivery models traditionally associated with the most advanced care delivery organizations.
Medical Director Oncology Clinical Research Hematology & Oncology Physician The Oncology Institute of Hope and InnovationMedical Director Oncology Clinical Research Hematology & Oncology PhysicianLas Vegas, NVWorking closely with Starling Oncology's Chief Medical Officer, physicians, clinical research coordinators, and research operations teams, the Medical Director will provide physician leadership for our clinical research program, expand patient access to clinical trials, strengthen Principal Investigator oversight, and help identify the trials that can have the greatest impact for the communities we serve. Formerly known as The Oncology Institute, Starling Oncology offers cutting-edge, evidence-based cancer care to a population of approximately 2.1 million patients, including clinical trials, transfusions, and other care delivery models traditionally associated with the most advanced care delivery organizations.
Manager of Hospitality Pyramid HealthcareManager of HospitalityHammonton, NJProvides supervision, operational oversight, coaching, and performance management support to hospitality services staff, including dining, housekeeping, janitorial, linen, and guest services personnel as assigned by facility structure. The Hospitality Manager partners with operational, clinical, facilities, and hospitality leadership to support service quality, client experience, employee engagement, operational efficiency, and regulatory readiness across assigned programs and facilities.
Senior Clinical Quality Operations Manager Eikon Therapeutics IncSenior Clinical Quality Operations ManagerMillbrae, CA$157,000–$189,000 / yearThis includes ensuring consistent execution of quality-by-design (QBD) principles across assigned clinical development programs and facilitating identification of Critical to Quality (CtQs) factors and associated risk assessments, establishing, and actively maintaining study-specific quality plans throughout the study lifecycle using a risk-based approach. In partnership with the Director of Process Management for Clinical R&D, the Head of Clinical Data Analytics and Reporting and the Head of Clinical Study Management, builds proficiency in leveraging technology and data to recognize and respond to new and emerging risks across the clinical portfolio, including how GCP applies to digital data management and novel trial technology.
Job Profile Clinical Research Nurse II Houston Methodist HospitalJob Profile Clinical Research Nurse IIHouston, TXHouston Methodist Research Institute supports research programs and infrastructure that enable faculty across the system to bring new scientific discoveries to patients as rapidly as possible through the full cycle of a cure from conceptual bench research, to prototyping and development, to clinical trials and FDA approval. Collects, processes and ships protocol-required lab specimens; maintains supply and equipment inventory; maintains appropriate laboratory certification as well as perform study closeout procedures including post-study documentation, return of study materials to the sponsor and data archiving.
Clinical Research Nurse Houston Methodist HospitalClinical Research NurseHouston, TXHouston Methodist Research Institute supports research programs and infrastructure that enable faculty across the system to bring new scientific discoveries to patients as rapidly as possible through the full cycle of a cure from conceptual bench research, to prototyping and development, to clinical trials and FDA approval. Collects, processes and ships protocol-required lab specimens; maintains supply and equipment inventory; maintains appropriate laboratory certification as well as perform study closeout procedures including post-study documentation, return of study materials to the sponsor and data archiving.
NewSenior Project Manager Tyler Service Soultions LlcSenior Project ManagerIjamsville, MDFull timeTyler Service Solutions, located in Ijamsville, MD, is seeking a dynamic Senior Project Manager with 10+ years of experience with commercial HVAC, plumbing, or mechanical contracting to join our growing team. The ideal candidate will work closely with customers to engineer solutions for their specific needs, combining technical expertise with professional management to deliver win-win outcomes.
Senior Project Manager - Advanced Energy Devices Intuitive Surgical IncSenior Project Manager - Advanced Energy DevicesSunnyvale, CAPrimary Function of Position: The Senior Project Manager - Advanced Energy Devices on the Future Forward PMO team will be responsible for leading the end-to-end development of advanced energy medical devices, including ablation and resection capital equipment. Certain information you provide as part of the application will be used for purposes of determining whether Intuitive Surgical will need to (i) obtain an export license from the U.S. Government on your behalf (note: the government's licensing process can take 3 to 6+ months) or (ii) implement a Technology Control Plan ("TCP") (note: typically adds 2 weeks to the hiring process).
NewClinical Research Associate DanaherClinical Research AssociateDeer Park, TexasRemote$75,000–$95,000 / yearBachelor’s degree (Life Sciences, Healthcare, or a related field preferred) with 3+ years clinical research experience ORMaster’s degree in field with 2+ years of related work experience, or demonstrated employment equivalency. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company’s sole discretion, consistent with the law.
Clinical Trial Manager, Clinical Operations Madrigal Pharmaceuticals IncClinical Trial Manager, Clinical OperationsConshohocken, PA$143,007–$168,465 / yearThe Clinical Trial Manager partners closely with other members within Clinical Operations, cross-functional functional areas, CROs, vendors, and investigational sites to drive successful study execution across multiple phases of clinical development. The role serves as the primary operational lead for assigned studies, mentors Associate Clinical Trial Managers and Clinical Trial Specialists, and contributes to process improvements that enhance operational efficiency while ensuring compliance with ICH-GCP, applicable regulatory requirements, and company SOPs.