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I position is available in the RSP Lab led by Dr. Sklavenitis Pistofidis. The RSP Lab (https://rsplab.org ) leverages advanced multi-omic technologies, coupled with experimental perturbations and
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clinical trials. Assess and document signs and symptoms of illness, reactions to treatment, changes in physical or psychological condition and general appearance in accordance with the IRB protocol assuring
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, amendments, correspondence and serious adverse event reports. Performs extensive audits and monitoring visits to determine protocol compliance, including the consent process and eligibility criteria. Performs
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tasks related to the admission/discharge/transfer process for all patient types. Performs accurate collection of patient demographic and insurance information, to be verified upon each patient
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; dataset specifications, data transfer specifications, and review of data management and handling plans. Develop and implement the data correction process, discrepancy resolution, data control activities
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-GCP guidelines, sponsor requirements, and institutional policies. Identify and escalate quality issues, data gaps, compliance risks, and process inefficiencies while recommending corrective action plans
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Good Manufacturing Practices (GMP). · Administer the Deviation, CAPA, and Change Control programs as Business Process Owner. · Author Deviations in collaboration with originating
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autonomy. You will work with Cherng Center leadership to grow the research program and its educational offerings. You will serve as a project manager, navigating the regulatory review process for each
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for Henderson Biorepository laboratory operations, including biospecimen collection and processing, Standard Operating Procedures (SOPs) and protocol oversight, process validation, quality control, regulatory
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patient reimbursements. Provide general administrative and operational support to the Research Team. Collaborate with multiple hospital departments for trial‑related needs and workflows. Process, ship, and