Executive Director, Clinical Development

Responsibilities:
- Provide strategic leadership for clinical development, including protocol design, regulatory strategy, and cross-functional execution
- Lead, mentor, and develop physicians, fostering a culture of scientific excellence, integrity, and collaboration
- Oversee preparation of key regulatory documents, including INDs, CTAs, protocols, and briefing packages
- Partner with Project Management and cross-functional leaders to drive governance, operational excellence, and program execution
- Guide clinical trial execution through investigator engagement, patient recruitment strategies, and quality oversight
- Build and maintain relationships with key opinion leaders, investigators, and external collaborators
- Represent Tango at scientific meetings, advisory boards, and other external engagements
- Support scientific communications, including publications, abstracts, and presentations

Qualifications/Requirements:
- MD with board certification or eligibility in Medical Oncology or Hematology/Oncology
- 11+ years of oncology clinical development experience in biotech or pharma (early- and late-stage)
- Expertise designing and executing oncology clinical trials involving targeted therapies
- Experience building and leading high-performing clinical development teams
- Deep knowledge of ICH-GCP, FDA, and global regulatory requirements

Skills:
- Strategic, collaborative leadership with excellent communication and cross-functional leadership skills
- Exceptional collaboration and ability to influence across diverse scientific and operational teams
- Resourceful, adaptable, execution-focused, with a passion for advancing innovative cancer therapies