
1001 - 5000 employees
Founded 1994
🏥 Healthcare
🧬 Biotechnology
💊 Pharmaceuticals
💰 $65M Post-IPO Equity on 2012-02
Healthcare • Biotechnology • Pharmaceuticals
Exelixis is a biotechnology and pharmaceutical company focused on developing cancer treatments through innovative research and development. The company is committed to advancing oncology by creating impactful cancer medicines, including biotherapeutics and small molecule therapies. Exelixis places a strong emphasis on clinical trials, collaborations, and a diverse range of treatment modalities, aiming to provide hope to cancer patients. Additionally, Exelixis is dedicated to sustainability, diversity, and community support, as reflected in their corporate values and practices.
🕒 April 30
🏄 California – Remote
💵 $283k - $402k / year
⏰ Full Time
🟠 Senior
👨⚕️ Medical Director
🦅 H1B Visa Sponsor
👻 Ghost score 35%
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1001 - 5000 employees
Founded 1994
🏥 Healthcare
🧬 Biotechnology
💊 Pharmaceuticals
💰 $65M Post-IPO Equity on 2012-02
Healthcare • Biotechnology • Pharmaceuticals
Exelixis is a biotechnology and pharmaceutical company focused on developing cancer treatments through innovative research and development. The company is committed to advancing oncology by creating impactful cancer medicines, including biotherapeutics and small molecule therapies. Exelixis places a strong emphasis on clinical trials, collaborations, and a diverse range of treatment modalities, aiming to provide hope to cancer patients. Additionally, Exelixis is dedicated to sustainability, diversity, and community support, as reflected in their corporate values and practices.
• Lead and execute early/late stage clinical trials for oncology products • Participate in the design/planning of clinical studies and help with the interpretation of study results • Establish and approve scientific methods for design and implementation of clinical protocols, data collection systems and final reports • Act as medical monitor for company sponsored trials • Support project teams with therapeutic area specific information • Analyze and interpret clinical trial data and prepare reports for regulatory agencies and publication • Ensure consistency of scientific and development strategies for oncology products
• MD (board certification or eligibility in Oncology or Hematology/Oncology desirable but not essential) required • Minimum of 8 years of post-residency experience • Drug development experience in biotechnology or pharmaceutical industry, or combination of academia and industry • Hands-on experience in the design, execution, and reporting of controlled clinical trials in oncology • Participated in clinical oncology studies with molecular targeted or immunological therapies • Understanding of basic science relevant to clinical oncology (biochemistry, immunology, molecular biology and/or genetics)
• 401k plan with generous company contributions • Group medical, dental and vision coverage • Life and disability insurance • Flexible spending accounts • Discretionary annual bonus program • Opportunity to purchase company stock • Long-term incentives • 15 accrued vacation days in their first year • 17 paid holidays including a company-wide winter shutdown in December • Up to 10 sick days throughout the calendar year
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