Senior Research Associate - Data Validation

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          "text": "<p><b><span>Senior Research Associate II </span></b></p><p><b><span>Location: Foster City, CA</span></b></p><p><b><span>Duration: 6 Months</span></b></p><p><b><span></span></b></p><p><span></span></p><p><b><span>Specific Responsibilities </span></b></p><p><span>-Provide operational support for acquisition and management of human biological samples collected for biomarker and other research purposes to help achieve the goals of the Biomarker Sciences Group. </span></p><p><span>- Plan, schedule and perform on-site receiving, accessioning, and distribution of samples from commercial vendors and academic collaborators as well as client clinical studies and Investigator Sponsored Trials (ISTs) to fulfill approved sample requests </span></p><p><span>- Monitor sample delivery, sample quality, and performance of vendor according to contract </span></p><p><span>- Maintain information on sample vendors regarding inventory, sample costs, sample collection services and performance </span></p><p><span>- Perform biomarker sample aliquoting to conserve samples on request and barcode and accession child samples into inventory. </span></p><p><span>- Maintain sample accessioning laboratory equipment and processes for receipt, accessioning, aliquoting, storage and distribution and associated controlled documents to ensure regulatory compliance. </span></p><p><span>- Collect, organize and curate information on samples collected from commercial vendors and academic collaborators as well as Gilead clinical studies, Investigator Sponsored Trials (ISTs) for loading into biomarker research database. </span></p><p><span></span></p><p><b><span>Essential Duties and Job Responsibilities: </span></b></p><p><span>- Maintain records of sample inventory and acquisition information and document curation activities according to business needs and in compliance with regulatory standards. </span></p><p><span>- Develop and follow biomarker sample management business processes and standard operating procedures (SOPs). </span></p><p><span>- Use biomarker research database and other reporting tools according to SOPs. </span></p><p><span>- Maintain accessioning laboratory processes and equipment in compliance with biosafety and quality standards and interact with infrastructure support groups. </span></p><p><span>- Work effectively with colleagues in Biomarker Sciences and Research Biology Groups to fulfill sample needs, and obtain input on scientific /technical issues. </span></p><p><span>- Work effectively with colleagues in Biomarker Sciences Group and other departments to align activities while performing responsibilities. </span></p><p><span>- Identify potential ways to streamline lab processes and/or management of sample information and work in team setting to implement. </span></p><p><span></span></p><p><b><span>Knowledge, Experience and Skills: </span></b></p><p><span>- MS in life science or clinical discipline with 4 or more years of relevant industry experience or BS in life science with 5 or more years of relevant industry experience. </span></p><p><span>- Laboratory experience in biological sample management </span></p><p><span>- Experience in biological sample data curation </span></p><p><span>- Experience in facilitating and managing quotes and contracts from external service vendors </span></p><p><span>- Experience using Excel and/or scientific/clinical databases; database validation experience a plus. </span></p><p><span>- Familiarity with drug development process and compliance requirements. </span></p><p><span>- Attention to detail and ability to track and help resolve open issues. </span></p><p><span>- Excellent teamwork, communication, decision-making and organizational skills required. </span></p><p><span>- Must be able to prioritize multiple tasks using planning, organizational and time management skills. </span></p><p><span></span></p>",
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