Biologics β’ Human therapeutics β’ Development of novel products
10,000+ employees
Founded 1980
𧬠Biotechnology
π Pharmaceuticals
π¬ Science
π° Post-IPO Debt on 2022-12
October 5
πΊπΈ United States β Remote
π΅ $251.7k - $326.1k / year
β° Full Time
π΄ Lead
π¨ββοΈ Medical Director
π¦ H1B Visa Sponsor
Biologics β’ Human therapeutics β’ Development of novel products
10,000+ employees
Founded 1980
𧬠Biotechnology
π Pharmaceuticals
π¬ Science
π° Post-IPO Debt on 2022-12
β’ Lead early phase clinical development of oncology compounds from first-in-human studies through proof of concept. β’ Define, design, and implement early phase clinical and translational projects. β’ Serve as an internal clinical expert in translational and clinical oncology. β’ Serve as medical monitor for clinical trials and assist in resolving major issues. β’ Present information internally and externally. β’ Coordinate clinical approaches to operational issues. β’ Provide guidance and assistance in the identification and management of oncology phase 1 collaborators. β’ Ensure appropriate training, recruitment, and development requirements for matrix team resources. β’ Evaluate external opportunities for partnering or licensing new oncology assets.
β’ MD or DO degree from an accredited medical school AND 2 years of clinical research and/or basic science research experience β’ Strong basic science or clinical research background in academia or industry β’ Prior experience authoring, monitoring, analyzing, and presenting oncology clinical trials β’ Effective presentation and communication abilities (both written and oral) β’ Ability to anticipate problems and find creative solutions β’ In-depth understanding of the scientific method and clinical applications based on medical, scientific, and practical rationale including working knowledge of biomarker methods and clinical imaging endpoints β’ A record of high-quality peer-reviewed publications β’ Experience functioning as a medical expert in a complex matrixed environment β’ Previous experience in early phase development and/or biomarker work β’ Previous experience in late-stage oncology clinical trials and regulatory filings β’ Demonstrated expertise in conducting translational and/or clinical oncology research β’ Expertise in Spotfire or other data analysis tools β’ Knowledge of GCP, EMA, and FDA policies β’ Expertise in authoring clinical sections of CTA or INDs
β’ Comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, β’ group medical, dental and vision coverage, β’ life and disability insurance, β’ flexible spending accounts. β’ A discretionary annual bonus program, β’ Stock-based long-term incentives β’ Award-winning time-off plans and bi-annual company-wide shutdowns β’ Flexible work models, including remote work arrangements, where possible
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