Senior Clinical Development Medical Director

Responsibilities

• Design and initiate study protocols in line with federal regulations and good medical practices
• Act as medical monitor for trials sponsored by the company
• Support project teams with oncology-specific information
• Analyze and report safety data in collaboration with the internal safety group
• Prepare reports for regulatory agencies and publications
• Engage with key opinion leaders and clinical investigators
• Ensure scientific consistency in development strategies for oncology products

Qualifications

• MD required; board certification in Oncology or Hematology/Oncology preferred
• Minimum of 8 years post-residency experience in drug development
• Hands-on experience in design and execution of oncology clinical trials
• Participation in studies with molecular targeted or immunological therapies
• Strong understanding of basic science relevant to clinical oncology

Benefits

• 401k plan with generous company contributions
• Group medical, dental, and vision coverage
• Life and disability insurance provided
• Flexible spending accounts available
• Discretionary annual bonus program or sales-based incentive for field staff
• Opportunity to purchase company stock and receive long-term incentives
• Up to 15 vacation days in the first year and 17 paid holidays, including winter shutdown
• Up to 10 sick days allowed each calendar year

Pay

$283,000 – $402,000 annually

Schedule

Remote - US based candidates only, no visa sponsorship available