Careers: Join Our Team

The VP of CMC is responsible for leading the overall planning, oversight and execution of assigned Aditum Bio Portfolio Companies’ CMC operations in all phases of development (pre IND-Phase II). This includes the strategic planning of the CMC program with Portfolio Companies and Board of Directors, as well as executing together with our strategic partners and Contract Manufacturers...

The Chief Medical Officer, Oblenio Bio will serve as a key member of Oblenio Bio’s leadership team, responsible for driving and overseeing the clinical development strategy and execution of Oblenio Bio’s pipeline, beginning with LBL-051, a differentiated trispecific T-cell engager. This physician-scientist will partner with Oblenio Bio’s CEO to shape the strategic direction of Oblenio Bio...

Aditum Bio is seeking a Vice President Clinical Development with experience in Phase II development who will own the overall design and execution of designated Portfolio Companies clinical trials. This includes the translation of preclinical data into clinical trial design and execution, clinical trial strategy and protocols.  The ideal candidate has a demonstrated...

The Vice President (VP) of Regulatory Affairs is responsible for developing and delivering regulatory strategies to support the advancement of Tempero Bio’s pipeline. The VP will demonstrate hands-on leadership across all stages of development and will ensure all filings are efficient, thorough and complete. The VP, Regulatory Affairs will lead and guide Tempero Bio’s interaction with the FDA. The ideal candidate...

Aditum Bio is seeking a highly-motivated Contracts Associate with transactional law experience in the life sciences industry to join its Legal Department. This opportunity has become available to support the increase in our contract volume as the preclinical and clinical pipelines of our portfolio companies continue to expand. This position reports to our Vice President, Head of Legal....

The Associate Director /Director R&D Quality Assurance will oversee the execution of Non-Clinical and Clinical Quality Assurance activities across the Aditum Bio portfolio companies, ensuring activities align with GLP and GCP expectations and the Quality Management System, and works closely with internal and external colleagues to develop systems and processes in-line with regulatory requirements, GCP, GLP, and internal quality processes...