Manager, Clinical Research Finance Operations (Office of Clinical Research) University of PennsylvaniaManager, Clinical Research Finance Operations (Office of Clinical Research)Long-Term Care Insurance: In partnership with Genworth Financial, Penn offers faculty and staff (and your eligible family members) long-term care insurance to help you cover some of the costs of long-term care services received at home, in the community or in a nursing facility. Penn Home Ownership Services: Penn offers a forgivable loan for eligible employees interested in buying a home or currently residing in West Philadelphia, which can be used for closing costs or home improvements.
Clinical Trials Lead (Lead Clinical Research Associate) AvaniaClinical Trials Lead (Lead Clinical Research Associate)RemoteFull timeFinally, you will provide CRA support, including such activities as assisting Clinical Research Associates with difficult or challenging situations or corrective actions, conducting co-visits and providing feedback, reviewing monitoring reports, and similar work. Avania's Lead Clinical Research Associate (CTL / Lead CRA) acts as the primary contact for study questions from the monitoring team, organizes team training and study updates, and generates necessary monitoring tools.
Clinical Research Coordinator to Home-Based CRA (Clinical Research Associate) Medpace, Inc.Clinical Research Coordinator to Home-Based CRA (Clinical Research Associate)RemoteOn-site and virtual/remote monitoring activities with a risk-based monitoring approach (including centralized data review) through our integrated Clinical Trial Management System to identify site deviations/deficiencies and corrective/preventive actions to bring a site back into compliance and mitigate risks moving forward. When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.
Clinical Research Manager - Breast Oncology Clinical Trials Dana-Farber Cancer InstituteClinical Research Manager - Breast Oncology Clinical TrialsRemoteThe Clinical Research Manager, in collaboration with the program’s physicians and research nursing staff, are responsible for the design, implementation and evaluation of their program’s clinical research activities (therapeutic and non-therapeutic), all related regulatory and compliance oversight, and direct supervision of their program’s clinical research staff. This Clinical Research Manager (CRM) position will work within the Breast Oncology clinical research program and manage the research team in the overall conduct of clinical trials using Good Clinical Practice under the auspices of the Principal Investigator and the Clinical Trials Office.
Assistant Clinical Research Manager - Breast Oncology Clinical Trials Dana-Farber Cancer InstituteAssistant Clinical Research Manager - Breast Oncology Clinical TrialsRemoteThese positions, in collaboration with the program’s Clinical research Managers physicians and research nursing staff, are responsible for assisting with the design, implementation and evaluation of their program’s clinical research activities, related regulatory oversight, and will provide day to day supervision of their program’s clinical research staff as needed. This Assistant Clinical Research Manager (ACRM) position will work within the Breast Oncology clinical research program and assist in the management of the research team in the overall conduct of clinical trials using Good Clinical Practice under the auspices of the Principal Investigator.
Assistant Clinical Research Manager - Center of Early Detection & Intervention Blood Cancers Interventional Clinical Trials Dana-Farber Cancer InstituteAssistant Clinical Research Manager - Center of Early Detection & Intervention Blood Cancers Interventional Clinical TrialsRemoteThe Assistant Clinical Research Manager (ACRM) position will work within the Center of Early Detection & Intervention Blood Cancers (CEDI BC) Interventional Clinical Trials clinical research program and assist in the management of the research team in the overall conduct of clinical trials using Good Clinical Practice under the auspices of the Principal Investigator. These positions, in collaboration with the program’s Clinical research Managers physicians and research nursing staff, are responsible for assisting with the design, implementation and evaluation of their program’s clinical research activities, related regulatory oversight, and will provide day to day supervision of their program’s clinical research staff as needed.
Wilmot Cancer Center - Clinical Trials Office - Clinical Research Nurse - Registered Nurse 2, Outpatient University of RochesterWilmot Cancer Center - Clinical Trials Office - Clinical Research Nurse - Registered Nurse 2, OutpatientThe CRN administers research interventions; collects patient data according to protocol specifications; evaluates the patient response to therapy; and integrates evidence-based practice into nursing practice to best protect the health and safety of research participants. This nursing role independently provides nursing care; identifies and communicates the impact of the research process on patient care; adjusts interventions based on findings; and reports issues/variances promptly to the research team.
Senior Clinical Trial Manager, Clinical Operations Gan & Lee PharmaceuticalsSenior Clinical Trial Manager, Clinical OperationsFull timeActively participate in the evaluation and selection of qualified external service providers (ESPs) (e.g., CROs), laboratory vendors, investigators, etc. and lead the contracting process with certain vendors which Gan & Lee contracts with directly. This position reports to the Head of Clinical Operations,This role is responsible for leading the development, planning, launch, conduct, closure, and submission of Gan & Lee sponsored clinical trials in accordance with all applicable federal, state, and local laws/regulations and Company’s policies, procedures, and guidelines.
Clinical Research Coordinator - BIDMC Clinical Research Coordinator Pool Beth Israel Lahey HealthClinical Research Coordinator - BIDMC Clinical Research Coordinator PoolThis position is embedded within the BIDMC Clinical Research Coordinator Core, a centralized resource serving investigators across departments and divisions throughout the medical center, and operates in affiliation with the institution’s Clinical Research Center, a member of Harvard Catalyst — Harvard’s Clinical and Translational Science Center. 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.
Supervisor Clinical Trials Office - Phase I Clinical Trials H. Lee Moffitt Cancer Center and Research InstituteSupervisor Clinical Trials Office - Phase I Clinical TrialsWith oversight from the responsible Clinical Trials Office Manager, and in collaboration with the faculty and investigators, the Clinical Trials (CTO) Supervisor provides basic day-to-day supervision and oversight of the assigned clinical research operations program staff to ensure implementation of good clinical practices as set forth by Federal regulations. Operationally, the CTO Supervisor focuses on the day to day conduct of studies through the life cycle of the protocol, trial coordination, and data quality assurance needs, providing problem solving and troubleshooting expertise.
Clinical Research Associate II / Senior Clinical Research Associate IREClinical Research Associate II / Senior Clinical Research AssociateAs a Clinical Research Associate within our sponsor-dedicated environment, you will play a critical role in the successful delivery of clinical trials, helping bring innovative therapies to patients worldwide. As we expand our partnerships with leading global sponsors, we are seeking experienced CRA II and Senior CRA professionals interested in sponsor-dedicated opportunities.
Clinical Innovation & Informatics- Clinical Expert Varian Medical Systems IncClinical Innovation & Informatics- Clinical Expert$119,920–$164,890 / yearIt is Siemens Healthineers' policy to comply fully and completely with all United States export control laws and regulations, including those implemented by the Department of Commerce through the Export Administration Regulations (EAR), by the Department of State through the International Traffic in Arms Regulations (ITAR), and by the Treasury Department through the Office of Foreign Assets Control (OFAC) sanctions regulations.". These requirements vary by client and may include, but are not limited to: Proof of valid identification (photo, driver's license, SSN) Criminal background checks Drug screens Immunizations (COVID-19, Hep B, MMR, Varicella, Influenza, Tetanus) Annual TB testing Healthcare training.
Principal Clinical Research Analyst - Class III Medical Devices (EU MDR Clinical Affairs Expert) Biotronik SE & Co KGPrincipal Clinical Research Analyst - Class III Medical Devices (EU MDR Clinical Affairs Expert)$165,000–$185,000 / yearWe are seeking a highly experienced Principal Clinical Research Analyst to provide strategic leadership and technical expertise in clinical evaluation, clinical evidence generation, and regulatory compliance for Class III medical devices. The ideal candidate will possess more than 7 years of experience in clinical affairs, clinical research, and regulatory support within the medical device industry, with extensive expertise in the requirements of the European Union Medical Device Regulation (EU MDR 2017/745).
Clinical Research Associate I - Clinical Trial Charge Monitoring Roswell Park Cancer InstituteClinical Research Associate I - Clinical Trial Charge MonitoringThis role supports the integrity of our research billing processes by reviewing charges, validating research‑specific modifiers and indicators, reconciling services against approved coverage analyses, and resolving discrepancies across patient accounts and research protocols. The Specialist collaborates closely with clinical trial coordinators, revenue cycle teams, compliance, and clinical departments to ensure adherence to federal, state, and payer‑specific clinical trial billing rules.
Sr. Clinical Research Associate / Field Clinical Specialist AvaniaSr. Clinical Research Associate / Field Clinical SpecialistRemoteFull timeAvania’s ClinOps Team establishes, maintains and supports clinical trials; as a key member of the team, our Sr CRA performs clinical trial oversight for the trials, verifying that the rights and well-being of human subjects are protected, and that reported trial data are accurate, complete, and verifiable (from source documents). Sr CRAs require skills in planning and preparation; sourcing and collecting information; prioritizing tasks and actions; and displaying a proactive attitude to assist in project planning and study execution.
Manager, Clinical Research University of RochesterManager, Clinical ResearchWorker Subtype: Regular Time Type: Full time Scheduled Weekly Hours: 40 Department: 400123 Radiation Oncology M&D Work Shift: UR - Day (United States of America) Range: UR URG 112 Compensation Range: $70,600.00 - $105,800.00 The referenced pay range represents the minimum and maximum compensation for this job. Ability to build collaboration among research team members, laboratory staff, patients and families, clinical services (requires tact, sensitivity, clarity, flexibility, empathy for patients) preferred.
Clinical Trials Registered Nurse, Oncology Research Clinical Trials, Full Time, Day The Valley HospitalClinical Trials Registered Nurse, Oncology Research Clinical Trials, Full Time, DayTo coordinate and implement clinical research protocols under the direction of the Director of Oncology Clinical Trials and Research Compliance, provide care to all or some of the patient's enrolled in each protocol, act as the patient advocate by assuring the safety, consistency, and accuracy of the treatment regimen as dictated by the protocol, and coordinate all nursing activities specifically related to the implementation of the treatment regimen. Must demonstrate effective oral and written communication skills, including speech clarity, understanding the information relayed, deductive and inductive reasoning skills (the ability to apply general rules to specific problems to produce answers that make sense and the ability to combine pieces of information to/from general rules or conclusion respectively).
Clinical Training and Program Development Specialist (Senior Clinical Research Associate) Oregon Health & Science UniversityClinical Training and Program Development Specialist (Senior Clinical Research Associate)RemoteRemoteWork as part of team to design targeted program development efforts, including statewide and local community education and marketing tailored to local communities, research studies, procedures, and day to day operations in support of training and technical assistance quality and practice improvement, research goals of priority interest to communities, and grant commitments. The position operates closely with other EC4E team members, EASA OHSU Flourish Clinic team members, and national and state partners to support statewide and national implementation of therapeutic practices and program improvement of substance use prevention and treatment in early psychosis care for individuals and family members.
Clinical Research Project Manager B University of PennsylvaniaClinical Research Project Manager BThe FTDC is seeking a Clinical Research Project Manager B (PM-B) who will be responsible for day-to-day management and oversight of the FTDC's federally funded observational research portfolio focused on young onset neurodegenerative diseases including frontotemporal degeneration (FTD), Alzheimer’s disease and related dementias. Long-Term Care Insurance: In partnership with Genworth Financial, Penn offers faculty and staff (and your eligible family members) long-term care insurance to help you cover some of the costs of long-term care services received at home, in the community or in a nursing facility.
Clinical Research Program Manager University of PennsylvaniaClinical Research Program ManagerThe Program manager will work closely with major internal (PI, data coordinators, researcher, laboratory technician, students, Institutional Review Board (IRB), etc.) and external (pharmaceutical collaborators, non-profit partners, external collaborators, oversight boards, CROs, Subcontractors, etc.) stakeholders to ensure regulatory compliance, completion of project milestones, and completion of all reporting requirements, and correct allocation of resources. Strong organizational skills; experience conducting studies in one or more of the above content areas preferred; excellent verbal and written communication skills essential to enable working with multiple members of research team; must be highly skilled in MS Word and Excel applications, understand medical records/patient charts organization and terminology.