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Senior Clinical Research Director - Oncology

Boston Oncology Institute
Boston
Salary Estimate
USD 280.000 – USD 340.000
Latest
Live Update
21 Mei 2026
Deadline
21 Mei 2027

Job Description

Are you ready to pioneer the next generation of life-saving oncology therapies? The Boston Oncology Institute is seeking a visionary Senior Clinical Research Director to lead our high-performing clinical development team. In this high-impact executive role, you will design and execute transformative oncology clinical trials from Phase I through Phase III, driving innovative therapeutic candidates from pipeline to approval.

We offer a world-class collaborative research environment in the heart of Boston's premier medical hub, backed by state-of-the-art facilities and a highly competitive executive compensation package. If you are passionate about patient-centric clinical innovation and translating scientific breakthroughs into clinical reality, join us in shaping the future of cancer care.

Responsibilities

  • Design, author, and execute robust clinical trial protocols for early-to-late stage oncology drug candidates.
  • Serve as the primary clinical spokesperson and medical monitor for active oncology trials, ensuring patient safety and rigorous data integrity.
  • Directly collaborate with global regulatory bodies (including the FDA and EMA) on IND/NDA submissions and clinical strategy.
  • Lead and mentor a multidisciplinary team of medical directors, clinical trial managers, and biostatisticians.
  • Analyze, interpret, and present complex safety and efficacy data to the executive leadership team and external scientific advisory boards.
  • Cultivate strong relationships with key opinion leaders (KOLs) and major academic research institutions globally.

Qualifications

  • Medical Degree (MD or MD/PhD) with active board certification in Oncology or Hematology.
  • A minimum of 8 years of clinical research and drug development experience within a biopharmaceutical or clinical research organization (CRO).
  • Demonstrated track record of successful IND/NDA submissions and clinical protocol design.
  • Deep expertise in GCP, ICH guidelines, and global regulatory requirements for oncology clinical trials.
  • Outstanding leadership capabilities with a proven history of managing highly specialized clinical teams.
  • Strong publication record in high-impact, peer-reviewed medical journals.

Required Skills

Oncology Clinical Research Regulatory Submissions FDA Compliance Clinical Trials Medical Leadership Drug Development Hematology

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