JOB DESCRIPTION: Serve as primary point of contact for Sponsored non‐clinical testing studies for medical products and independently execute them. Serve in multiple roles as needed, including Non‐GLP Principal Investigator and GLP Study Director on safety studies and efficacy studies. Participate in cross‐functional study teams, particularly with Preclinical Operations staff to ensure the requirements/tasks of the respective protocols and the execution of the actions/milestones called out in the corresponding project plan are achieved. Collaborate with senior Program Managers, management, Sponsors and 3rd party service providers to develop repeat business and expand capabilities. Assist with business development tasks including fielding inbound requests for services, developing cost estimates independently and attending conferences and business meetings according to the marketing plan and customer needs.  


MINIMUM QUALIFICATIONS: Bachelor's degree from accredited 4‐year college or university in biology, physiology, molecular biology, engineering or related field required. Minimum of 8 years of experience in lab animal or pre‐clinical biomedical testing in CRO or academic laboratory required. 2 years of medical product research work as a Principal Investigator involving AAALAC, GLP and USDA protocol and regulations. 4 years of experience with project management. Demonstrated experience with MS Office required; knowledge of project management, publishing and accounting software applications, e.g. Microsoft Project, Adobe Acrobat, Quickbooks, etc. is preferred. Experience in managing cost centers, P+L, strategic planning and forecasting preferred. Hands on operational experience and ability to interact successfully with staff at many economic, educational, and professional levels within and outside the organization. 


PREFERRED QUALIFICATIONS: Graduate degree in biology, physiology, molecular biology, engineering or related field required. 10 years or more experience in lab animal or pre‐clinical biomedical testing in CRO or academic laboratory required.  4 years of medical product research work as a Principal Investigator and Program Manager or equivalent position. 2 years work as a GLP Study Director involving AAALAC, and USDA protocol and regulations.  6 years of experience with project management.  Demonstrated experience with MS Office required; knowledge of project management and accounting software applications, e.g. Microsoft Project, Quickbooks, etc. is required.  Experience in managing cost centers, P+L, strategic planning and forecasting preferred.  Hands on operational experience and ability to interact successfully with staff at many economic, educational, and professional levels within and outside the organization, including Director and Executive level scientists and business managers.   
NOTE: Candidate may be hired at Program Manager or Senior Program Manager depending on level of experience. 

Please contact Evan Goldberg, Program Director for this posting

Email:  evan.goldberg@t3labs.org