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and behavioral tools, and follow them for >2 years, with repeated follow-up assessments. Responsibilities include conducting 1-year follow-up study visits and centralizing the recruitment process as
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staff on technical procedures, equipment operation, and laboratory maintenance. 4. Schedules and coordinates research activities. Identifies and recruits study participants. Orders and maintains
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into electronic data capture systems, providing sponsors with requested clinical and regulatory information, and resolving data queries in a timely manner. Laboratory responsibilities include processing fluid
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into electronic data capture systems, providing sponsors with requested clinical and regulatory information, and resolving data queries in a timely manner. Laboratory responsibilities include processing fluid
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into electronic data capture systems, providing sponsors with requested clinical and regulatory information, and resolving data queries in a timely manner. Laboratory responsibilities include processing fluid
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into electronic data capture systems, providing sponsors with requested clinical and regulatory information, and resolving data queries in a timely manner. Laboratory responsibilities include processing fluid
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IRB applications, clinical data collection, drafting DSMB minutes, data quality management, performing lab experiments such as ELISA and colorimetric assays, biospecimen processing, shipping and storing
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information related to research data. Codes data accordingly to research specifications. Uses a computer terminal to input and retrieve data and to generate reports. 3. Processes and summarizes data using
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interfolio) Please submit application materials electronically to Interfolio at https://apply.interfolio.com/178923 . The review process will begin January 5, 2026. We will continue to accept applications
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related to research data. Codes data accordingly to research specifications. Uses a computer terminal to input and retrieve data and to generate reports. 3. Processes and summarizes data using scientific