Associate Medical Director / Medical Director

Seattle Genetics   •  

Bothell, WA

Industry: Pharmaceuticals & Biotech

  •  

Less than 5 years

Posted 64 days ago

This job is no longer available.

Summary:

The Associate Medical Director will be responsible for developing and implementing the life cycle strategy of brentuximab vedotin, including in combination with checkpoint inhibitors. He/she will be responsible for the conduct of multiple clinical trials in hematologic malignancies, and will function as a scientific and medical resource for the Clinical Development department at Seattle Genetics as well as a liaison to development partners.

Responsibilities:

  • Contribute to the strategic development of clinical programs
  • Development of clinical protocols and amendments, investigator brochures, and clinical study reports
  • Lead clinical study teams and provide appropriate medical monitoring for ongoing clinical studies
  • Evaluation of safety, pharmacology, and efficacy data from ongoing and completed studies
  • Prepare manuscripts, abstracts and presentations for scientific meetings and advisory boards.
  • Conduct literature reviews and prepare summaries to support clinical development programs
  • Medical resource for design and interpretation of clinical and preclinical programs to support existing and new development candidates
  • Collaborate with company leadership, team, cross-functional stakeholders, and investigators/medical professionals

Qualifications:

  • MD or MD/PhD
  • Clinical oncology experience; Board certification in oncology or hematology preferred
  • 2-5 years industry experience in oncology drug development preferred
  • Demonstrated passion for helping patients with cancer and for the science of oncology
  • Global perspective and mindset, with ability to work effectively with colleagues from myriad cultures, backgrounds and geographies