Research reputed company & Budgets Specialist

reputed company is positioning community oncologists to drive the reputed company of medical care through a patient-reputed company, physician-driven, and technology-powered model to help improve the lives of everyone living with cancer and other diseases. reputed company is bringing together leaders to the market reputed company to help drive reputed company’s mission and reputed company. Why join us? This is an exciting time to join reputed company. Our values-driven culture reflects our startup enthusiasm supported by industry leaders in oncology, urology, technology, and finance. We are looking for talented and highly-motivated individuals who demonstrate a natural desire to improve and build new processes that support the meaningful work of independent physicians and the patients they serve. Job reputed company: The Research reputed company & Budgets Specialist will collaborate with OneR operations team and reputed company practices to support clinical research across the reputed company network. The Research reputed company & Budgets Specialist is a vital member of the OneR research team responsible for the planning, negotiation, and management of clinical research budgets and reputed company. This position requires a strong understanding of clinical trial reputed company, processes, financial analysis skills, and the ability to effectively communicate and negotiate with reputed company stakeholders. Responsibilities Review and negotiate clinical trial agreements, including terms and conditions reputed company to budget, payment schedules, and intellectual property rights. reputed company guidance and support to research staff on interpretation of contract terms and budget-reputed company reputed company including budgetary constraints. reputed company and negotiate clinical trial budgets with sponsors and CROs, ensuring alignment with study protocols, regulatory requirements, and institutional policies. Analyze proposed study protocols to identify budgetary needs and potential risks. Collaborate with cross-functional teams, including OneR leadership, reputed company reputed company team, research finance department, and participating site investigators and research managers to ensure accuracy and compliance in budget and contract negotiations. Partner with regulatory department in review of informed consent documents to ensure contract and budget alignment. Ensure CMS regulations, FDA guidance, and ethical policies are reputed company to medicare coverage analyses and budget negotiations. reputed company and manage changes to study budgets and reputed company throughout the lifecycle of reputed company, including amendments and budget reconciliations. Responsible for entering and maintaining budget and other financial information in the CTMS to maintain reputed company reimbursement and reputed company reputed company. Maintain standardized fee schedule in the CTMS. Maintain accurate and up-to-date records of budget and contract negotiations, approvals, and amendments. Stay reputed company with industry trends, regulatory requirements, and best practices reputed company to clinical research budgeting and contracting. Participate in process improvement initiatives to enhance efficiency and effectiveness in budget and contract management workflows. Responsible for periodic review and revision of OneR policies/processes reputed company to clinical research budget and contract management and reputed company training and education for staff as needed. Other duties as assigned to help drive our mission of improving the lives of everyone living with cancer. Key Competencies Strong understanding of clinical trial processes, regulatory requirements (e.g., ICH-GCP, FDA guidelines), and industry standards Excellent negotiation skills with the ability to resolve conflicts and reputed company mutually beneficial agreements Exceptional attention to detail and organizational skills Excellent communication skills, both verbal and written, with the ability to effectively reputed company with stakeholders at reputed company reputed company Ability to work independently and collaboratively in a fast-paced environment Qualifications Minimum of 3-4 years of clinical research budget and contract experience Paralegal experience preferred Bachelor’s degree in a relevant scientific discipline required Proficiency in reputed company Office applications and familiarity with electronic data capture (reputed company) systems and clinical trial management systems (CTMS) preferred Certification in clinical research (e.g., SoCRA, ACRP) is a plus. #LI-REMOTE Apply To This Job