Join us on our mission to change lives

Aura biosciences is a clinical-stage company developing a novel, virus-like drug conjugate technology platform for the treatment of multiple cancer indications.  We are looking for talented, enthusiastic and committed professionals who match our passion and commitment to science – and to the patients battling cancer.

Open Positions: Clinical

Contract Regional CRA – East Coast/Midwest

The Contract Regional CRA candidate will be responsible for overall site management including, but not limited to site qualification, initiation, interim monitoring, and trial close-out activities for studies in accordance with Good Clinical Practices (GCPs) and applicable local and international regulations and Standard Operating Procedures (SOPs). Responsibilities also include ensuring the quality of data submitted from trial sites and the timely submission of data, including appropriate reporting and follow-up for all safety events, by site personnel, as well as Investigator Site File review and investigational product accountability. This particular role will focus on Ophthalmology, specifically choroidal melanoma.
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Clinical Trial Associate/ Associate Clinical Trial Manager, Clinical Operations

This position will provide clinical trial management support to the Clinical Operations team in completion of all required tasks to meet departmental and project goals and support the ongoing conduct of clinical trials in Aura’s lead program in ocular melanoma, as well as other trials in the future.
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Director/Senior Director Clinical Development

Aura Biosciences is actively recruiting for a Director/Senior Director Clinical Development. The successful candidate will have significant experience in ophthalmology R&D, be a critical member of the R&D leadership team, work in partnership with the Executive Medical Director to lead Aura’s clinical development pipeline and be a key contributor to the Company’s drug development programs.
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Open Positions: Finance

No positions available.

Open Positions: Manufacturing

Lab Operations Manager

Reporting to the CMC Technical Lead, the Lab Manager will oversee day to day activities in support of laboratory provisioning, maintenance and upkeep. Additionally, this person will serve as liaison between research staff and external vendors to facilitate efficient lab operations as needed. The ideal candidate should have previous lab experience including inventory management, shipping/receiving, reagent preparation, lab safety practices, etc.
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Principal Scientist (Biochemistry / Molecular and Cell Biology)

This role on the Analytical Sciences (AS) team contributes to Aura’s efforts to develop safe and effective therapies using virus-like particle (VLP)-based technologies. This role is expected to spend 15-40% at the bench.
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Clinical Supply Chain Manager

The Clinical Supply Chain Manager will report to the Director Technical Program Lead CMC to support Aura’s clinical program. The Clinical Supply Chain Manager is responsible for overseeing packaging and labeling of Aura’s products and clinical supply planning.
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Research Associate, Process Development

Aura Biosciences is seeking motivated individuals to join a team of scientists focused on the development of virus like particles (VLPs) for treatment of ocular melanoma. The RA/Sr. RA (depending on experience) will work with the Process Development group to execute operations for the production and purification of VLPs to support of preclinical and clinical programs.
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Manager/Associate Director of Quality, GCP

The GCP Quality Assurance candidate will manage activities related to the development, maintenance and oversight of GCP activities related to the Clinical Trial activities sponsored by Aura Biosciences. The primary responsibilities will be to ensure both quality and compliance of company sponsored clinical trials with respect to internal Standard Operating Procedures, applicable regulatory requirements (US FDA, ICH, and country specific), along with current industry standards and practices.
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Open Positions: Regulatory

Sr Specialist / Manager, Regulatory Affairs

Reporting to the Head of Regulatory Affairs, the Senior Specialist / Manager of Regulatory Affairs will work with internal and external stakeholders to prepare regulatory submissions, archive records, track commitments, etc. in a growing organization.
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