Company Overview

Tango Therapeutics is a biotechnology company dedicated to discovering novel drug targets and delivering the next generation of precision medicine for the treatment of cancer.

Using an approach that starts and ends with patients, Tango leverages the genetic principle of synthetic lethality to discover and develop therapies that take aim at critical targets in cancer.

This includes expanding the universe of precision oncology targets into novel areas such as tumor suppressor gene loss and their contribution to the ability of cancer cells to evade immune cell killing.

The Tango labs and offices are located at 201 Brookline Avenue, in the Fenway area of Boston, Massachusetts

 

Summary

Tango has an exciting new opportunity to join the team as our first Director, Clinical Sciences. In this role you will lead the development, planning, execution, and evaluation of clinical studies to ensure scientific integrity and accurate interpretation of the data. In this role you will report to the Senior Vice President, Head of Clinical Development.

 

Your Role:

  • You will function as the lead clinical scientist on all Tango programs
  • Collaborate with cross-functional teams to ensure timely execution of clinical trials in compliance with regulatory requirements and Good Clinical Practice (GCP)
  • Work closely with clinical operations, biostatistics, pharmacovigilance, and other clinical teams to ensure alignment on project goals and timelines
  • Provide scientific input and support to commercial teams for product positioning and marketing strategy
  • Author and review trial documents, such as medical monitoring plans, clinical trial protocols, informed consent, and clinical aspects of clinical study reports
  • Contribute to the preparation of regulatory documents, including, but not limited to, IND applications and clinical study reports
  • Liaise with regulatory authorities as needed to support clinical development efforts
  • Working with clinical sites and CROs for training activities and responding to clinical inquiries
  • Lead the monitoring team in the review and interpretation of clinical data to generate insights to inform decision making and strategy
  • Mentor junior clinical scientists and study teams fostering a culture of innovation and scientific rigor
  • Lead initiatives to enhance clinical development processes and practices within the organization
  • Prepare and present data summaries and findings to internal stakeholders and external partners
  • Additional duties and responsibilities as required

 

What You Bring:

  • MD, PhD, PharmD, MS within a relevant scientific discipline
  • At least 10 years’ experience in clinical science, or research
  • At least 3 years’ experience in oncology
  • Demonstrated experience in designing and managing clinical trials, including knowledge of regulatory guidelines and GCP
  • Strong analytical skills with proficiency in statistical analysis and interpretation of clinical data
  • Excellent written and oral communication skills, with the ability to convey complex scientific concepts to diverse audiences
  • Experience working in a fast-paced environment

 

We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.

 

 

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