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 newly opened position at Tango, you will collaboratively manage a global clinical trial though the development of a novel drug. You will bring robust trail management experience, with strong communication, vendor management and project management skills. You will develop an understanding of the needs of the many teams necessary to do comprehensive clinical operations work, with a collaborative outlook. You will manage workloads to meet expedited project timelines in a rapid and dynamic environment.
Your Role:
You will manage clinical trials from start-up through close-out to ensure both internal and external deliverables are on time and on budget while facilitating collaboration across functional areas
Work with the cross functional clinical team to coordinate the relevant and timely exchange of information/materials to support clinical trial delivery and execution
Oversee and contribute to the development of clinical trial project timelines and ensure communication and understanding of risks/challenges; establish plans and monitor metrics; ensure that timelines are accurate and comprehensive
Proactively manage clinical trial outsourced partners, including identification of risk, to ensure trial deliverables and performance goals are met
Manage the day-to-day contact with CRO counterpart; daily review and identification of potential issues or problems with sites and communicate/escalate to clinical team as necessary
Collaborate with the CRO to keep clinical study database current and accurate
Proactively manage and track project scope and change orders, for clinical trial operations
Additional duties and responsibilities as required
What You Bring:
Bachelor’s degree in life science or allied health field (e.g. nursing, medical or laboratory technology)
5 years industry experience mostly in clinical operations
Experience working in a global development organization
Experience in setting up a global study and giving input into study design
Experience working in a matrix organization
Experience working in a full outsourcing model
Experience in sponsor oversight including site management oversight
End-to-end study experience
Experience in late phase/pivotal study conduct
Experience in supporting health authority inspection (preparation)
Experience in managing/overseeing global studies conducted in different geographic regions
Experience in assessing operational risks and implementing risk mitigation actions
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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Salary range
$120,000—$180,000 USD