Role Summary
Tango Therapeutics is seeking an experienced oncologist to serve as Vice President Clinical Development for our PRMT5 programs in development for MTAP-deleted cancers. This strategic leadership role will drive clinical development strategy and execution as we advance into Phase 3 development. You will serve as the clinical and scientific voice for the program. This role reports directly to the SVP, Head of Clinical Development and plays a critical part in advancing Tango's precision oncology pipeline.
Responsibilities
- Drive pivotal phase III programs for TNG462 by leading protocol development, amendments, and operational execution, while partnering with the Head of Clinical Development on strategy and key decisions.
- Work cross-functionally with Clinical Operations, Regulatory, Medical Affairs, Biostatistics, and others; partner with Medical Affairs on publications, abstracts, and investigator meetings; represent Clinical Development in industry partnerships; and design and initiate study protocols and amendments in compliance with GCP/ICH and regulatory requirements.
Team Development & Management
- Directly manage clinical scientists supporting the PRMT5 program
- Provide mentorship and development opportunities for emerging clinical leaders
- Foster a culture of scientific rigor, operational excellence, and collaboration
Regulatory & Scientific Documentation
- Provide strategic input into regulatory meeting planning, preparation, and slide deck development
- Lead authorship and provide close oversight of regulatory documents including protocols, INDs, briefing documents, and responses to health authority questions
- Support the development and compilation of regulatory filings including INDs, CTAs, and NDAs
Operations & Governance
- Partner with Project Management on clinical governance meeting agendas and cross-functional alignment
- Establish and drive operational improvement initiatives
- Work closely with clinical teams to support patient recruitment strategies and maintain strong relationships with Principal Investigators
- Monitor adherence to protocols and ensure consistency in quality standards across all program activities
External Engagement & Scientific Leadership
- Build and maintain relationships with key investigators, thought leaders, and clinical trial sites
- Act as liaison between company and clinical investigators
- Represent PRMT5 clinical development at scientific conferences and investigator meetings
- Review/co-author medical publications emerging from clinical trial results
What You Bring
Required Qualifications
- MD degree with board certification or eligibility in medical oncology or hematology-oncology
- Minimum 15+ years of clinical development experience in oncology in the biotechnology or pharmaceutical industry, with at least 5 years in late-stage (Phase 2/3) programs
- Hands-on experience in the design, execution, and reporting of clinical trials in oncology, evaluating small molecule targeted agents and/or immunological therapies
- Direct experience with IND filings required
- Demonstrated experience leading global clinical programs from protocol design through regulatory submission
- Strong scientific writing skills with proven track record of regulatory document authorship
- Experience managing and mentoring clinical development teams
- Deep understanding of ICH-GCP, FDA regulations, and global regulatory requirements
- Effective leadership, people management, team-oriented and results-oriented style with strong interpersonal, verbal, written, communication, and presentation skills
- Flexible, creative, optimistic, and resourceful style and attitude
Preferred Qualifications
- Experience with targeted oncology therapies or precision medicine approaches
- Late-stage clinical development experience (Phase 3) and NDA/MAA filing and approval process
- Experience with novel mechanism agents
- Prior experience in biotech environment
- Experience working with pharmaceutical industry partnerships or collaborations
- Creative problem-solving approach with ability to identify and implement methods, techniques, procedures, and evaluation criteria to achieve results