Medical Director, Oncology Clinical Development (Solid Tumors)

📋 Description

• With appropriate supervision, manages the design and implementation of study protocols for a
• Has responsibility for oversight of clinical studies, monitoring overall study integrity, and
• Contributes to design, analysis, interpretation, and reporting of scientific content of protocols
• May serve on a Clinical Strategy Team as the clinical representative for the protocols for which
• Participates in opinion leader interactions related to the disease area(s); partners with Medical
• Stays abreast of professional information and technology through conferences, medical literature

🎯 Requirements

• Medical Doctor (M.D), Doctor of Osteopathy (D.O.), or non-US equivalent of M.D. degree with
• Ability to run a clinical research study with appropriate supervision.
• Strong desire to collaborate in a cross-functional setting.
• Clinical trial experience in the pharmaceutical industry, academia, or equivalent is preferred.
• Knowledge of clinical trial methodology, regulatory and compliance requirements governing clinical
• Ability to interact externally and internally to support global scientific and business strategy.

🎁 Benefits

• We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick)
• This job is eligible to participate in our long-term incentive programs.