We are currently seeking 3 Curation Scientists for a 6+ month contract in Santa Clara:
• Research, interpretation, and validation of germline variants
• Research, interpretation, and validation of somatic variants
• Prepare reports on biomarker findings
• Import of reports into database
• Maintain records of research and procedures
• Curation of patient clinical data and molecular data
• Preparation of XML documents for encoding data
Develops the strategies, designs, implements, monitors and evaluates clinical trials and other associated clinical development programs for assigned molecules or drugs. Medical Director will be assigned responsibilities for Ph II and Ph III clinical trials, programs and/or other projects. Work closely with internal cross-functional stakeholders, external investigators, various corporate partners and regulatory authorities.
Plays a lead role in providing clinical input into the ...
Responsible for the medical oversight of global pharmacovigilance activities of clinical trials and product development. Post-marketing safety experience is highly desirable.
Support Safety Operations to establish and maintain policies and procedures for the Clinical Drug Safety Department.
Perform or provide oversight for the medical review of serious adverse event reports to ensure accuracy, integrity and completeness of safety information, and to ensure consistency of medical ...
Jan 27 -
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