Careers

at Talaris

Careers

Talaris is hiring!  We are an equal-opportunity employer offering competitive benefits and a mission-driven culture that focuses on improving outcomes for the patients we serve.  Our open positions are listed below:

To apply, please send your CV to careers@talaristx.com with the position you are applying for in the subject line.

If the position you are looking for is not listed, please check back frequently for new open positions, as our team is growing rapidly.

QA Document Control Specialist

The QA Document Control Specialist will be based in Louisville, KY reports to the Manager, Quality Control. Responsible for maintaining and sustaining change control, training and documentation processes.

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Head of Portfolio and Program Management

Talaris is seeking a Head of Portfolio and Program Management to develop and lead the program management function. This newly created position will play a key role in establishing program management processes and tools, identifying risks and developing mitigation plans, and coordinating cross-functional plans and timelines across all programs.

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Senior Accounting Analyst

The Senior Accounting Analyst will be based in Louisville, KY and reports to the Controller. The Senior Accounting Analyst will work hand in hand with the Controller to continue to improve the financial reporting and compliance processes as well as identify areas of needed improvement across the finance function.

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Materials Management Supervisor

The Materials Management Supervisor, to be based in Louisville, KY reports to the Manager, Supply Chain, is responsible for maintaining sufficient levels of materials for cell therapy manufacturing at Talaris Therapeutics. The Materials Management Supervisor will oversee GMP receiving, shipping, and kitting activities.

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Clinical Trial Manager/Sr. CTM, CLINICAL OPERATIONS

Manages and tracks overall operations of a clinical study including project plans, budget, and resource management. Leads development of study operational plans and is able to provide input into other functional area plans as needed. Provides excellent oversight of the CRO, vendors and sites. Ensures compliance with GCP and regulatory guidelines. Position reports to Director, Clinical Operations.

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