169 evolution-"https:"-"https:"-"https:"-"https:"-"https:"-"https:"-"BioData" positions at Baylor College of Medicine
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institutional processes, fostering coordinator development, and ensuring seamless communication across programs, departments, and affiliated institutions. This position is a central, institution-level supervisory
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defining biological phenotypes. This position will conduct complex and independent research investigations and will assist in the planning, development, and implementation of experiments related to normal
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care, and program development while leading efforts to achieve Foundation for the Accreditation of Cellular Therapy (FACT) accreditation for cell therapy and subsequently for stem cell transplantation
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projects, develop and implement new technologies and protocols, and will provide guidance and technical support to all users of the Core. Job Duties Participates in the development of project budgets
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and build academic and industry partnerships to support sponsored research, grants, and at-cost service models. Job Duties A central responsibility of this role is the development, auditing, and
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research projects. This position provides opportunities for high-impact research, interdisciplinary collaboration, and professional development in a leading academic medical center. Job Duties • Design
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development. Minimum Qualifications Bachelor's degree in a Basic Science or related field. Four years of related experience may substitute for degree requirement. No experience required. Work Authorization
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. Collaborates with central finance, grants administration, human resources, and other institutional departments to ensure alignment and efficiency. Financial Strategy and Operations Leads the development and
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. Responsibilities will include cost assessment, budget development, financial set-up, resource allocation, and preparation of quarterly reports for budget accountability. Employees with CRA certification are eligible
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oncology and hematology human subjects projects including the development, compilation, and submission of regulatory documents to IRBs/IECs, FDA, and other agencies (e.g., INDs, IDEs, 1572s, annual reports