Amgen
Amgen is a global leader in biotechnology, focusing on the development and commercialization of innovative medicines made from living cells. The company aims to treat serious illnesses, often targeting diseases with limited therapeutic options. Amgen emphasizes scientific innovation and is committed to ethical research, patient safety, and environmental sustainability. It actively engages in clinical trials and is known for its contributions to the fields of cancer treatment and obesity management among others.
Biologics • Human therapeutics • Development of novel products
Medical Sciences Director - Late Development, Obesity and Endocrinology Diseases
March 5
Amgen
Amgen is a global leader in biotechnology, focusing on the development and commercialization of innovative medicines made from living cells. The company aims to treat serious illnesses, often targeting diseases with limited therapeutic options. Amgen emphasizes scientific innovation and is committed to ethical research, patient safety, and environmental sustainability. It actively engages in clinical trials and is known for its contributions to the fields of cancer treatment and obesity management among others.
Biologics • Human therapeutics • Development of novel products
📋 Description
• Contribute to late phase clinical development of Obesity • Collaborate on teams to define, design, and deliver late phase clinical results • Provide subject matter expertise in clinical and translational trial science • Support medical monitor in clinical trials and assist in resolving issues • Present information internally and externally, anticipating and actively managing problems • Provide guidance and assistance in the identification and management of Obesity collaborators, consultants, and/or Clinical Research Organizations • Ensure integrity of protocols and/or components of clinical plans • Provide clinical input into & implementation of clinical trial(s), their delivery • Review and analyze clinical trial data to ensure accuracy, completeness and adherence • Conduct thorough data quality assessments in the context of a data monitoring plan
🎯 Requirements
• Doctorate degree and 4 life sciences/healthcare experience • Master’s degree and 7 life sciences/healthcare experience • Bachelor’s degree and 9 years life sciences/healthcare experience • 5 years of pharmaceutical clinical drug development experience • Proven track record of clinical trial process improvement in Obesity or any metabolic diseases • Strong communication and presentation skills to clearly communicate scientific concepts and data to leadership committees • Experience with designing, monitoring, and implementing clinical trials and interpreting test results in compliance with Good Clinical Practice standards and regulatory requirements • Understanding of conducting study data readout activities, including data cleaning, data base lock, data extract, producing outputs of data • Experience drafting high level submission documents for regulatory submissions • Experience in clinical data analysis such as Spotfire or other data analysis tools
🏖️ Benefits
• 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, including remote and hybrid work arrangements, where possible
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