Medical Director Oncology Clinical Development Lead

1 day ago

Chicago, Illinois, United States AbbVie Full time
Job Overview

AbbVie is seeking a highly skilled Medical Director to lead the clinical development of our oncology programs. As a key member of our team, you will be responsible for overseeing the direction, planning, execution, and interpretation of clinical trials or research activities.

Key Responsibilities
  • Manage and demonstrate ownership of the design and implementation of one or more clinical development programs in support of an overall Product Development Plan.
  • Participate in cross-functional teams to generate, deliver, and interpret high-quality clinical data supporting overall product scientific and business strategy.
  • Oversee project-related education of investigators, study site personnel, and AbbVie study staff.
  • Have overall responsibility for oversight of clinical studies, monitoring overall study integrity, and review, interpretation, and communication of accumulating data pertaining to safety and efficacy of the molecule.
  • Responsible for assessment and reporting of serious adverse events per corporate policy and regulations for those protocols on which assigned.
  • Design, analysis, interpretation, and reporting of scientific content of protocols, Investigator Brochures, Clinical Study Reports, regulatory submissions and responses, and other program documents.
  • May oversee the work of Associate Medical and/or Scientific Directors, and of Clinical Scientists working on the same or related programs.
  • Provide in-house clinical expertise for the molecule and disease, coordinating appropriate scientific and medical activities with internal stakeholders as they relate to ongoing clinical projects.
  • May participate in due diligence or other business development activity.
Requirements
  • Medical Doctor (M.D.), Doctor of Osteopathy (D.O.) or non-US equivalent of M.D. degree with relevant therapeutic specialty in an academic or hospital environment.
  • At least 0-2 years of clinical trial experience in the pharmaceutical industry, academia, or equivalent.
  • Ability to run a clinical research program of moderate complexity with minimal supervision.
  • Ability to perform and bring out the best in others on a cross-functional global team.
  • Ability to interact externally and internally to support a global scientific and business strategy.
  • Knowledge of clinical trial methodology, regulatory and compliance requirements governing clinical trials and experience in development of clinical strategy and the design of study protocols.
  • Must possess excellent oral and written English communication skills.
Additional Information

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion.

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