
201 - 500 employees
𧬠Biotechnology
π Pharmaceuticals
π¬ Science
π° $300M Post-IPO Equity - Xenon Pharmaceuticals on 2023-11
Biotechnology β’ Pharmaceuticals β’ Science
Xenon Pharmaceuticals Inc. is a clinical-stage biotechnology company focused on neuroscience drug discovery and development. It leverages human genetics, ion-channel biology, and novel chemistries to create selective modulators of central and peripheral nervous system ion channels. Its lead late-stage investigational candidate, azetukalner, is being developed for epilepsy and depression. The company emphasizes patient-centered research, clinical trials, and support for people affected by neurological and psychiatric disorders.
π 4 days ago
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201 - 500 employees
𧬠Biotechnology
π Pharmaceuticals
π¬ Science
π° $300M Post-IPO Equity - Xenon Pharmaceuticals on 2023-11
Biotechnology β’ Pharmaceuticals β’ Science
Xenon Pharmaceuticals Inc. is a clinical-stage biotechnology company focused on neuroscience drug discovery and development. It leverages human genetics, ion-channel biology, and novel chemistries to create selective modulators of central and peripheral nervous system ion channels. Its lead late-stage investigational candidate, azetukalner, is being developed for epilepsy and depression. The company emphasizes patient-centered research, clinical trials, and support for people affected by neurological and psychiatric disorders.
β’ Lead and manage data management activities for assigned products, initiatives and/or clinical trials β’ Design clinical trial databases, including CRF Development, Database Validation, and Data Review tools β’ Oversee external data management vendors β’ Optimize data management and collection activities β’ Maintain current knowledge of relevant issues related to data management β’ Propose, draft, and maintain relevant Standard Operating Procedures β’ Act in accordance with Company policies
β’ Bachelorβs degree in a scientific, medical, computer science or related field; Masterβs degree preferred β’ A minimum of 5 yearsβ management level experience in a pharma or biotech environment β’ Strong experience in data management-related activities β’ Thorough understanding of the clinical trial process and regulatory requirements, including CDISC β’ Strong experience in design and validating EDC databases and performing data review β’ Familiar with safety laboratory data management and dictionary coding for adverse events and medications β’ Experience in CNS, pediatric rare disease area and e-diary database design and implementation are preferred β’ Experience in CRO management β’ Ability to be hands-on with database cleaning β’ Excellent leadership and interpersonal skills β’ Proven ability to collaborate in high performing teams β’ Ability to travel up to 10%, both domestically and internationally.
β’ Medical, dental, vision insurance β’ Short- & long-term disability β’ Accidental death & dismemberment β’ Life insurance programs β’ Employee Assistance Program β’ Travel insurance β’ Retirement savings programs with company matching contributions β’ Paid vacation, personal days, sick days, and an end-of-year company shutdown β’ Tuition Assistance program for advanced degrees β’ Employee development program
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