At LENZ Therapeutics, Our TEAM is focused on innovative science to improve vision.
Our team is expanding and looking for top candidates join our team.
LENZ offers competitive employee benefits:
- Generous medical, dental, and vision health insurance plans
- Short-term, long-term, and life/AD&D insurance
- Paid vacation days, 1holidays, and additional sick time
- 401(k) Retirement Plan with company match
Learn more about LENZ and follow us on LinkedIn.
Project Manager
The Project Manager Role is responsible for planning, organizing, and overseeing the execution of projects from start to finish, ensuring that project goals are met within the specified timeframe and budget. With the Ph3 CLARITY study underway, the Project Manager will be expected to monitor project progress around the success of the study and timelines related to commercialization, including the management of potential risks, communication to stakeholders, and identification of areas of improvement.
Clinical Operations Manager
The Clinical Operations Manager (COM) will be a key member of the LENZ team and play a critical role in ensuring that our upcoming clinical trials are executed successfully. The Clinical Operations Manager will assist the Director of Clinic Operations Support. This role will be expected to continually assess and adjust patient flow for increased efficiencies, coordinate and delegate administrative and clinic maintenance responsibilities such as patient access, patient education sheets, patient experience surveys, chart creation and other special projects. In conjunction with the Director of Clinic Operations, the COM will establish procedures for reception, intake, eligibility determination, and medical records filing, including scheduling of staff and task management.
Clinical Research Associate
As our Clinical Research Associate (CRA), you will be a key member of the LENZ team and play a critical role in ensuring that our upcoming clinical trials are executed successfully, as well as support our overall strategy as we prepare our FDA submission, gain approval, and bring to commercialization our lead asset. The CRA will be expected to perform independent on-site and remote monitoring procedures such as but not limited to site qualification, site initiation, interim monitoring, site close-out, end of study visit, and overall site management.