Registered Nurse - Oncology Clinical Research - Full Time Jupiter Medical CenterRegistered Nurse - Oncology Clinical Research - Full TimeJupiter Medical Center is the only hospital in Palm Beach, Martin, St. Lucie and Indian River counties to receive a 4-star quality and safety rating from the Centers for Medicare & Medicaid Services (CMS). Outstanding physicians, state-of-the-art facilities, innovative techniques and a commitment to serving the community enables Jupiter Medical Center to meet a broad range of patient needs.
Clinical Research Infusion RN - PRN H. Lee Moffitt Cancer Center and Research Institute HospitalClinical Research Infusion RN - PRNFacilitates clinical research activity by performing ongoing assessments, administering nursing care and protocol therapy, monitoring of patients, delivering patient education, and documenting care for patients enrolled on clinical trials. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process, please contact one of the Human Resources receptionists by phone at 813-745-7899 or by email at HRReceptionists@moffitt.org.
Clinical Research Infusion RN H. Lee Moffitt Cancer Center and Research Institute HospitalClinical Research Infusion RNFacilitates clinical research activity by performing ongoing assessments, administering nursing care and protocol therapy, monitoring of patients, delivering patient education, and documenting care for patients enrolled on clinical trials. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process, please contact one of the Human Resources receptionists by phone at 813-745-7899 or by email at HRReceptionists@moffitt.org.
NewSenior Clinical Trial Manager IRESenior Clinical Trial ManagerAs a Senior Clinical Trial Manager at ICON, you will manage clinical trial operations activities, supporting your team and stakeholders to deliver high-quality outcomes across our clinical programmes. Your focus will be on coordinating clinical trial management delivery, resolving issues, and developing team capability.
NewClinical Research Operations Manager AdventHealthClinical Research Operations ManagerManages all duties necessary for effective and compliant clinical research study coordination across multiple therapeutic areas, including planning, organizing, and managing all activities related to clinical research operations and execution of timelines. Collaborates with managers in Research Services, Study Intake, Portfolio Management, and clinical study coordinators to develop study budgets for all research projects within supported therapeutic areas.
Clinical Quality Compliance Manager N-Power Medicine IncClinical Quality Compliance ManagerRemote$134,985–$163,247 / yearQuality Operations & Execution: Implement and maintain best-in-class quality systems in alignment with N-Power's quality strategy and regulatory requirements (e.g., FDA, ICH, 21 CFR Part 11, ISO 9001) Foster a culture of quality excellence, compliance, and continuous improvement across the organization Manage, mentor, and support the day-to-day-activities of a lean, high-performing quality team, optimizing capabilities, resources, and workflows in alignment with N-Power's corporate goals and roadmap. Quality Systems Management: Maintain, optimize, and serve as the primary administrator for the electronic Quality Management System (eQMS) in compliance with ISO 9001 and applicable regulatory requirements Directly manage core QMS processes, including but not limited to document control, training management, risk management, internal and external audits, CAPA, nonconformances, change management, and supplier management.
NewClinician & Clinical Research Director (CCRD) Yale UniversityClinician & Clinical Research Director (CCRD)In conjunction with the Principal Investigator, the CCRD will provide oversight of all programmatic activities and staff including, but not limited to, the following: Provide senior clinical, operational, administrative, and strategic leadership for multidisciplinary clinical research and healthcare delivery programs supporting Yale research initiatives in conjunction with the Principal Investigator. The CCRD serves in a senior leadership capacity across clinical, administrative, research, and policy domains and is responsible for strategic growth planning, program expansion into additional clinical and community settings, workforce development, and implementation of scalable and sustainable clinical research operations in conjunction with the Principal Investigator.
Senior Clinical Data Manager (Remote, US) MMSSenior Clinical Data Manager (Remote, US)(Multiple States)RemoteFull timeProvides oversight and resolves all issues in data management study processing activities including CRF tracking and data entry, integration of external electronic data (e.g., lab data) with clinical database, data validation and review, query processing and resolution, adverse event and medication coding, SAE reconciliation, database lock and database QC audits. Oversees and develops data management study documentation including Case Report Forms, CRF Completion Guidelines, Database Design via annotated CRFs, Validation specifications (edit checks), and Data Management Plan.
Clinical Research Nurse C (OBGYN - Pregnancy and Perinatal Research Center) University of PennsylvaniaClinical Research Nurse C (OBGYN - Pregnancy and Perinatal Research Center)The research nurse duties include but are not limited to management of research patient care, collection of medical and medication history, physical assessments, completion of patient visits according to protocol specifications, completion of source documents and case report forms (CRFs), reporting of non-serious and serious adverse events, maintenance of regulatory files, and preparation for monitoring visits and audits. With the support of the study team, the research nurse will carry out state of the art clinical trials and other research studies, including consenting, screening, and enrolling eligible subjects, managing the treatment of patients throughout their participation in the study including education about any adverse effects they might experience, provide oversight and coordination of research testing and follow-up.
Per Diem Clinical Research Nurse - Home Visits Science 37Per Diem Clinical Research Nurse - Home Visits$50–$55 / hourWith interest/expertise in Science 37's decentralized model of care delivery, the Mobile Research Nurse will perform delivery of care to participants as well as collaborate with brick and mortar sites, if indicated, for shared clinical trial implementation. Science 37's Nursing Solutions Group brings together expert nurses who share a passion for organizing, planning and implementing mobile clinical nurse services to participants in clinical trials.
Supervisor Clinical Research Operations Pre Award H. Lee Moffitt Cancer Center and Research InstituteSupervisor Clinical Research Operations Pre AwardSkills/Specialized Training: • Clinical Research Expertise - Strong knowledge of various funded clinical trials, including the financial management aspects, budget development, payment term negotiations, and regulatory compliance. • Strong Communication Skills: Excellent verbal and written communication skills, with the ability to negotiate and collaborate effectively with internal and external stakeholders, including clinical research teams, sponsors, and vendors.
Regulatory Coordinator - Neely Center for Clinical Cancer Research Tufts MedicineRegulatory Coordinator - Neely Center for Clinical Cancer ResearchIn addition, this role focuses on performing the following Administration Project Management duties: Serves as a liaison between the general project management office and the team members engaging in planning, reviews the status of projects and budgets, manages schedules, prepares status reports, and assesses project issues and develops resolutions to meet productivity, quality, and client-satisfaction. Works collaboratively with a variety of personnel at all levels, including faculty and study team members of the Neely Center for Cancer Clinical Research (NCCCR) and external institutions, cooperative groups, clinical trials experts, representatives from the pharmaceutical industry, federal agencies, and other research organizations.
Clinical Research Project Manager I Dana-Farber Cancer InstituteClinical Research Project Manager IReporting to disease group managers and/or Clinical Trials Office (CTO) leadership the Clinical Research Project Manager I identifies project plan variances and develops contingency plans to maintain project milestones. Administrative Support: Schedule research team meetings and conference calls, facilitate mailings, and perform other project-related administrative tasks to ensure effective communication and coordination among team members and external collaborators.
Clinical Research Coordinator I - Heme | Myeloid H. Lee Moffitt Cancer Center and Research InstituteClinical Research Coordinator I - Heme | MyeloidThese positions work closely with patients, patient families, study sponsors (from smaller pioneer biotech companies through large pharmaceutical companies), and the Clinical Trial Team that includes physicians, pharmacists, nurses, data monitors and data managers. Our Clinical Research Coordinators come from a variety of backgrounds and experiences, including social sciences (public health, social work, sociology, psychology, communications, and more), biological sciences, business, and humanities.
Director of Engineering, Lynd Clinical 25madisonDirector of Engineering, Lynd ClinicalOur model combines owned site infrastructure with a proprietary AI platform that analyzes longitudinal medical records to identify, screen, and enroll high-quality participants with speed and precision: driving faster enrollment and better trial outcomes for both sponsors and trial participants. Our engineers actively use tools such as Claude Code, Cursor, Gemini, and other AI-powered development systems to accelerate software delivery, reduce repetitive work, and increase individual impact.
Clinical Research Financial Analyst II Dana-Farber Cancer InstituteClinical Research Financial Analyst IIUnder general supervision of the Clinical Research Budgets Manager, the Clinical Research Financial Analyst (CRFA-II) is responsible for financial planning, developing budgets, negotiating financial agreements with funding sources and vendors, and ensuring effective financial management throughout the lifecycle of Clinical Research studies. Works closely with study teams and Clinical Research Finance teams to address financial inquiries and support study-related financial management through regular meetings and communications.
Clinical Research Coordinator -- Surgery FIRST Program Beth Israel Lahey HealthClinical Research Coordinator -- Surgery FIRST ProgramResponsible for screening research subjects for participation in clinical research projects, enrolling research subjects onto these studies, monitoring protocol implementation, completing required forms, reporting results, maintaining regulatory paperwork, and entering data into databases. Customer Service: Ability to provide a high level of customer service to patients, visitors, staff and external customers in a professional, service-oriented, respectful manner using skills in active listening and problem solving.
Clinical Research Coordinator - Surgery FIRST Program Beth Israel Lahey HealthClinical Research Coordinator - Surgery FIRST ProgramResponsible for screening research subjects for participation in clinical research projects, enrolling research subjects onto these studies, monitoring protocol implementation, completing required forms, reporting results, maintaining regulatory paperwork, and entering data into databases. Customer Service: Ability to provide a high level of customer service to patients, visitors, staff and external customers in a professional, service-oriented, respectful manner using skills in active listening and problem solving.
Clinical Trial Manager The Steely GroupClinical Trial ManagerRemote, CARemoteOversee development and maintenance of study documents such as Study Timelines, Vendor Management Plan, Risk Management Plan, Informed Consent Form, Monitoring Oversight Plan, CRFs, Study Reference Manual, dashboards, etc. Responsible for the day-to-day management of assigned operational aspects, such as CRO/vendor management, drug supply management, management of clinical sites, etc. for assigned region(s) or study(s).
Clinical Biostatistics (Adjunct Pool), Henry E. Riggs School of Applied Life Sciences Keck Graduate InstituteClinical Biostatistics (Adjunct Pool), Henry E. Riggs School of Applied Life SciencesLocated in beautiful Claremont, California, Keck Graduate Institute is a member of the prestigious Claremont Colleges, a consortium of five undergraduate liberal arts colleges, two graduate institutions, and The Claremont Colleges Services, which provide shared institutional support services. Required Knowledge, Skills and Abilities: Individuals must possess knowledge, skills and abilities to successfully perform the essential function of the position, or be able to explain or demonstrate how the essential functions may be performed, with or without, reasonable accommodations, using some other combination of skills and abilities.