Perform independent, accurate, and timely review and analysis of research billing inquiries to resolve, provide guidance, or triage to appropriate staff for resolution.
Develop and implement education and communication outreach activities that will provide and document accurate and continuous research billing education programs for the OHSU community.
Collaborate with Epic Research Revenue Cycle and CTMS Support to provide input, evaluate, and test clinical research billing functionality in Epic and the CTMS.
The Clinical Research Services Office (CRSO) functions as a central service office, overseeing industry-sponsored research contracting, clinical research billing compliance, OHSU's clinical trials management system, and federal reporting compliance. The CRSO also helps to set some of the standards and policies for the conduct of clinical research at OHSU, engages clinical research staff in community building, training, and education, and partners with other OHSU departments and teams via the Clinical Research United (CRU) initiative.
Serve as leader of the local study team on assigned studies.
Manage and maintain accurate country level plans including timelines and budgets.
Implement startup and site activation plans at various levels.
Jobgether uses an AI-powered matching process to ensure applications are reviewed quickly, objectively, and fairly. They identify top-fitting candidates and shares this shortlist directly with the hiring company.
Works in partnership with the primary point of contact to provide high quality, accurate data management support for complex studies.
Maintains a working knowledge of parallel processes that are integrated with the function of clinical trial data, and is responsible for the compilation, registration and submission of data.
Supports the implementation of custom, research project-specific data workflow solutions for data collection, management, reporting and analytics.
The University of Rochester is committed to the ideal of “Ever Better” and the values we share: equity, leadership, integrity, openness, respect, and accountability. It is one of the world’s leading research universities.
Partner with clinical trial staff and consortium study teams to communicate start-up process, milestones, and timeline goals.
Identify research costs and develop comprehensive budgets for single & multi-site industry sponsored clinical trials and IITs.
Monitor financial performance relative to budget and explain variances and trends.
Fred Hutchinson Cancer Center is a nonprofit organization focused on adult cancer treatment and research. They are based in Seattle and have a global leadership in bone marrow transplantation, HIV/AIDS prevention, immunotherapy and COVID-19 vaccines.
Manages the financial, regulatory, patient management, and human resources functions associated with conducting clinical trials.
Supervises a staff of 2 - 5 employees; trains new clinical trials staff; tracks enrollment, sponsor payments, and salary.
Provides leadership in business development and assists residents in preparing research projects by facilitating IRB submissions and protocol writing.
Emory University is a leading research university fostering excellence and attracting world-class talent to innovate today and prepare leaders for the future. They welcome candidates who can contribute to the excellence of their academic community.
Assist Clinical Project Manager in the development and management of company-sponsored global clinical trials.
Provide support in site recruitment, site initiation, site payments and site close-out.
Help to provide guidance to clinical sites on a daily basis including protocol interpretation and protocol safety compliance.
ImmunityBio, Inc. is a commercial-stage biotechnology company that develops cell and immunotherapy products that are designed to help strengthen each patient’s natural immune system. The company is publicly traded with headquarters in Southern California, offering a collaborative environment with professional development opportunities.
Maintain project documentation including presentations, plans, agendas and overall project timelines.
Act as the primary liaison between technical teams and external partners to ensure alignment on project goals.
Provide proactive communication by setting clear expectations and providing project updates before client requests.
Medrio seeks smart and capable individuals to expand product capabilities, grow their business, and better serve customers. They value collaboration, ingenuity and creating a culture of excellence, offer great benefits and promote an atmosphere of work/life balance, including flexible work schedules and locations.
Develop a short-term strategy for clinical and industry trials.
Oversee clinical trial operations, including regulatory compliance, budgeting, contracting, and performance metrics.
Manage and lead a team of clinical research coordinators and leaders across the health system
CommonSpirit Health is building a healthier future for all through its integrated health services. As one of the nation's largest nonprofit Catholic healthcare organizations, CommonSpirit Health delivers more than 20 million patient encounters annually and has more than 157,000 employees.
Analyze and improve UM business workflows, including clinical assessments, rules, and documents.
Validate Health Services programs against business requirements and acceptance criteria.
Partner with medical directors and cross‑functional teams to review, evolve, and update InterQual and custom clinical criteria.
Wellmark is a mutual insurance company owned by its policy holders across Iowa and South Dakota, and it has built its reputation on over 80 years of trust. They are motivated by the well-being of their members and committed to sustainability and innovation.
Management and operational delivery of clinical elements within a trial.
Successful execution of assigned trials and ensuring completion of deliverables.
Identify challenges to study timelines and offer creative action plans.
Precision for Medicine is a precision medicine CRO, integrating novel clinical trial designs, operational and medical experts, and biomarker and data analytics solutions. They are passionate about rare diseases and oncology, working across other therapeutic areas, with high-energy, dedicated professionals.
Responsible for managing research activities at sites participating in Worldwide’s clinical research projects.
Involved in all stages of the clinical study, including identifying potential sites and performing study start-up activities.
Conduct study initiation visits and ensure compliance with informed consent and reporting potential safety events.
Worldwide Clinical Trials is a global, midsize CRO that pushes boundaries, innovates and invents to cure the world’s most persistent diseases. They are a global team of over 3,500+ experts, bright thinkers, dreamers and doers that are changing the way the world experiences CROs.