Director, Biostatistics

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

In this new role, reporting to the Senior Director, Biometrics you will be working with cross‑functional clinical teams responsible for statistical activities across Tango’s clinical programs, including overseeing statistical deliverables outsourced to clinical CROs. This is an exciting opportunity to make an impact in the development of transformative therapies that may change patients’ lives. You will be a good communicator, collaborative, self-motivated, and forward‑thinking.

Your Role:

You will serve as a biostatistics expert for Tango’s clinical programs

Provide strategic input to optimize trial designs in early phase dose escalation studies and late phase registrational studies

As a biostatistics representative, proactively collaborate with internal and external CRO team members to coordinate the planning and execution of statistical deliverables

Conduct statistical modeling to enable robust and efficient statistical designs and address identified or potential statistical issues arising with studies

Contribute to clinical protocol development, including authoring or review of the Statistics section and reviewing of other sections by applying statistical principles

Author or review the development of statistical analysis plans for clinical trials and oversee the development of tables, figures, and listings, and associated deliverables

Review electronic case report form (eCRF) designs to ensure data collection meets the requirements of statistical analyses

Provide statistical input for clinical documents

Perform QC/QA of statistical deliverables including validation of key analysis results

Perform ad hoc statistical analyses as needed

Contribute to clinical study reports, including authoring of statistical methods, and interpretation of study results

Accountable for assigned statistical activities in support of IND/NDA/MAA or other regulatory submissions; provide thorough review for required components of regulatory submissions including appropriate datasets, define files, reviewer's guides, and other relevant documents

Address statistical questions/comments from FDA and other regulatory agencies, or IRB/ECs

Support and contribute to the preparation of publications, including manuscripts, posters, and oral presentations

Lead standardization and process improvement efforts for Biostatistics function, and contribute to cross-functional process improvement efforts including the definition of biostatics templates and standards

Represent Tango regarding statistical issues in meetings with external parties including regulatory agencies and corporate partners

Support inspection readiness activities as needed

Develop and maintain advanced competencies in statistical methodology and advanced trial designs, particularly in oncology drug development

Additional duties and responsibilities as required

What You Bring:

PhD in statistics or related discipline; MS with appropriate years of directly relevant experience

At least 10 years’ experience in the pharmaceutical or biotech industry

Oncology experience required

Experience in the design, analysis, and reporting of clinical trials

Experience in INDs, NDAs, MAAs, or other regulatory submissions

In-depth knowledge of statistical methods for clinical trials

Knowledge of FDA, EMA, and ICH regulations and guidelines

Proficient in statistical programming (SAS and R)

Ability to lead statistical efforts for multiple studies

Fluent in data standards, including SDTM and ADaM

Experience in outsourced statistical services provided by CROs

Ability to work independently and act with initiative to address issues

Excellent written and oral communication skills, including the ability to effectively communicate statistical concepts in a clear and concise manner

#LI-hybrid

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. Salary range $191,200 — $286,800 USD