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Research Data Specialist - Leukemia
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- Responsible for the preparation of accurate and detailed instructions for all clinical research sampling required by Leukemia Department protocols and which involve the effort and commitment of the Leukemia Clinical Research Services laboratory.
- For designated protocols, provides schematic solutions for effective protocol research sample collection, processing and shipment to sponsor-designated labs across the nation and worldwide.
- Participates in site initiation visits (SIV), audits and monitor visits, obtains clarification of outstanding issues related to sample collection, processing and shipment, and captures all the information addressed in draw sheets and team presentations.
- Addresses sponsor queries related to all aspects of research sample collection, processing and shipment on study protocols, including accuracy of time points and quality of final product.
- Maintain a query database of all the queries received from industry sponsors such as ECG, bone marrow, PK, blood samples, urine, and so forth.
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