Evan Goldberg Email and Phone Number

- Project manage and coordinate the financial and business operations of a multi-year and multi-institutional research contract with ARPA-H. - Coordinate research, regulatory, translational and other activities between multiple academic institutions, industry partners and federal agencies. - Work with PIs, Staff Scientists, Postdocs, Administrative Officials and other relevant members of the team to ensure SOW and milestones are accomplished on time and within budget.- Manage and assemble progress reports that include technical progress, data produced, financial reporting and technology translation up to once a month with ARPA-H program directors. - Provide quarterly / ad hoc data access for progress verification to ARPA-H - Provide other support that is necessary to achieve the SOW / milestones of the contract.

Sr. Research Engineer designation through T3 Labs and GCMI's affiliation with Georgia Tech.

- Serves as the GCMI Academic Liaison to Georgia Tech and other university-based sponsors. Meet with academic faculty members to understand their translational and commercialization needs. Facilitate translational research and commercialization activities through GCMI service lines.- Manages the development of new relationships and maintains existing university-based programs for medical products at GCMI.- Develops programs for faculty/student engagement.-- Leads GCMI educational efforts for university faculty, staff and students (i.e., seminars, guest lectures, etc.).

- Management of Program Leadership staff and the portfolio of non-clinical testing programs and studies. Lead preclinical strategic planning, budgeting and business development activities. Serves as the preclinical marketing liaison. Serves as Test Facility Management delegate.

- Led the development of new and maintenance of existing multiple Sponsored non-clinical testing programs for medical products.- Served a primary point of contact for orthopedic program studies and executed each directly in multiple roles as needed, including GLP Study Director on large, complex safety and efficacy studies.- Collaborated with TFM, management, Sponsor and 3rd party service providers to ensure program needs are anticipated and met.

- Lead the development of new and maintenance of existing multiple Sponsored non-clinical testing programs for medical products. - Serve a primary point of contact for orthopedic program studies and execute each directly in multiple roles as needed, including GLP Study Director on large, complex safety and efficacy studies. - Collaborate with TFM, management, Sponsor and 3rd party service providers to ensure orthopedic program needs are anticipated and met. - Assist the department director with management of Program Management staff and the portfolio of non-clinical testing programs and studies.

- Serves a primary point of contact for Sponsored non-clinical testing studies for medical products and independently execute them. - Serves in multiple roles as needed, including GLP Study Director on large, complex safety and efficacy studies. - Leads cross-functional study teams, particularly junior Program Management and 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. - Collaborates with management, Sponsor and 3rd party service providers to develop repeat business and expand capabilities.

- Manages preclinical research projects for medical device companies of varying complexity ranging from model development and initial prototype testing to GLP safety and efficacy studies. - Responsible for generating budgets, writing protocols, coordinating study logistics and generating reports.

- Assisted Program Management staff in the day-to-day execution of studies for sponsors, which included collecting data and preparing results for final reports. - Ensured that the required materials, supplies, resources, and information were prepared for each milestone. - Assisted management and Program Managers in ensuring the administrative requirements of the studies and sponsors’ timelines were achieved.

- Collect patient and research data and assist in the design and development of new research protocols.- Train and supervise students and staff.- Participate in the writing of grants, scientific papers and abstracts.- Present research findings at scientific conferences.

- Performed theoretical simulations using Visual C++ and SIMM to examine elderly gait in order to develop efficient rehabilitation strategies. - Analyze experimental data to determine differences between treadmill and overground walking.

- Worked as a Teaching Assistant for Biomechanics of Human Movement course.- Responsibilities included grading coursework, assisting students with assignments, and compiled survey results to improve interactive teaching modules. - Evaluated and redesigned interactive teaching modules for use at universities nation-wide.