Medical Director - Early Clinical Development, Oncology

October 5

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Logo of Amgen

Amgen

Biologics β€’ Human therapeutics β€’ Development of novel products

10,000+ employees

Founded 1980

🧬 Biotechnology

πŸ’Š Pharmaceuticals

πŸ”¬ Science

πŸ’° Post-IPO Debt on 2022-12

Description

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.

Requirements

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

Benefits

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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