Clinical Development Director – Early Development Oncology

🕒 Agosto 26

🇺🇸 Estados Unidos – Remoto (EUA)

💵 $274.788 - $371.773 / ano

⏰ Tempo Integral

🔴 Especialista

👔 Diretor

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Amgen

SiteLinkedInTodas as Vagas

10.000+ funcionários

Fundada em 1980

🏥 Saúde

🧬 Biotecnologia

💊 Farmacêutico

💰 $28.500.000.000 Post-IPO Debt em 2022-12

Healthcare • Biotechnology • Pharmaceuticals

A Amgen está comprometida a liberar o potencial da biologia para pacientes que sofrem de doenças graves, descobrindo, desenvolvendo, fabricando e fornecendo terapias humanas inovadoras. Esta abordagem começa utilizando ferramentas como genética humana avançada para desvendar as complexidades das doenças e entender os fundamentos da biologia humana.

Descrição

• Lead the early phase clinical development of oncology compounds from first-in-human studies through proof-of-concept • Collaborate on teams to support the design and delivery of early phase clinical trials • Support protocol development, study start-up, data review, monitoring and analysis activities • Contribute to the design and implementation of early clinical development strategies for oncology therapeutic candidates • Contribute to clinical development plans, clinical study protocols, informed consents, Investigator Brochures, and Ethics Committee and regulatory agency submissions • Review and evaluate clinical study safety, efficacy, pharmacodynamic and pharmacokinetic data • Contribute to the strategy and use of clinical biomarkers to facilitate drug development • Collaborate with Precision Medicine, Research, Late Development, Regulatory, Safety and Commercial colleagues • Contribute to evaluating external licensing or partnering opportunities within oncology therapeutic areas • Collaborate with external experts to provide biomedical expertise and strategic guidance to oncology early development teams

🎯 Requisitos

• MD or DO degree from an accredited medical school • 2 years of industry or academic clinical research/drug development experience • Board certification or eligibility in Oncology (preferred) • Residency training in Oncology and relevant subspecialty (preferred) • Experience in basic research and/or clinical trial methodology (preferred) • 3+ years of relevant drug development experience in the pharmaceutical industry and/or academia, preferably in early stage clinical trials • Experience collaborating with pharmaceutical sponsors • Experience designing, monitoring and implementing clinical trials and interpreting trial results • Demonstrated leadership qualities and ability to conduct studies as part of a team • Experience within a matrix environment and contributing to decision-making and alignment to meet challenging timelines • Publication track record • Excellent interpersonal and presentation skills • Ability to communicate effectively with internal stakeholders, external partners and collaborators • Sponsorship for this role is not guaranteed

🏖️ Benefícios

• A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions • Group medical, dental and vision coverage • Life and disability insurance • Flexible spending accounts • A discretionary annual bonus program • Stock-based long-term incentives • Award-winning time-off plans • Flexible work models where possible • Career development opportunities • Work/life balance • Financial plans with opportunities to save towards retirement or other goals