Senior Clinical Development Medical Director

The primary role of the Senior Clinical Development Medical Director is to lead and execute early/late stage clinical trials for oncology products in development. Responsibilities include designing and initiating study protocols, acting as a medical monitor for company sponsored trials, and analyzing and interpreting clinical trial data.

Requirements

• MD (board certification or eligibility in Oncology or Hematology/Oncology desirable but not essential) required with a minimum of 8 years of post-residency experience.
• Drug development experience in biotechnology or pharmaceutical industry, or a combination of academia and industry.
• Hands-on experience in the design, execution, and reporting of controlled clinical trials in oncology.
• Understanding of basic science relevant to clinical oncology (biochemistry, immunology, molecular biology and/or genetics).
• Proven ability to effectively work in a cross-functional/matrix environment.
• Strong interpersonal, influencing, presentation, and written and verbal communication skills
• Strong organizational and time management skills

Benefits

• 401k plan with generous company contributions
• group medical, dental and vision coverage
• life and disability insurance
• flexible spending accounts
• discretionary annual bonus program
• sales-based incentive plan
• opportunity to purchase company stock
• long-term incentives
• 15 accrued vacation days in their first year
• 17 paid holidays
• up to 10 sick days throughout the calendar year