Job Description
Description Remote Our client seeks a Strategic Global Feasibility Consultant to drive feasibility and site selection for CAR-T expansion studies across North America, Europe, and Asia-Pacific. The consultant will design and execute regional and site-level assessments, align outputs with timelines and enrollment goals, and mitigate operational risks unique to cell therapy. The role requires expertise in oncology and cell and gene therapy operations, CRO collaboration, and knowledge of global CAR-T site networks. The impact includes accelerated start-up and optimized country and site strategy within regulatory and logistical constraints. Due to client requirements, applicants must be willing and able to work on a w2 basis. For our w2 consultants, we offer a great benefits package that includes Medical, Dental, and Vision benefits, 401k with company matching, and life insurance. Rate: $105.00 to $135.00/hr. w2 Responsibilities Lead global feasibility strategy for CAR-T clinical trials across North America, Europe, and Asia-Pacific. Design and execute country and site feasibility assessments across key regions including the U.S., EU, UK, and Asia. Identify, evaluate, and recommend high-performing investigative sites with CAR-T administration capabilities. Assess site readiness for cell therapy trials, including apheresis, manufacturing logistics, cryopreservation, and chain-of-identity and chain-of-custody requirements. Partner with Clinical Operations to align feasibility outputs with study timelines and enrollment targets. Analyze epidemiology, standard of care, competitive landscape, and enrollment potential across countries. Develop site selection strategy balancing speed, quality, and geographic diversity. Support CRO oversight related to feasibility deliverables and site identification. Provide recommendations to mitigate risks related to enrollment, startup timelines, and operational complexity. Ensure feasibility planning aligns with regulatory and logistical constraints in each region. Experience Requirements 10+ years of experience in Clinical Operations with a strong focus on feasibility and site selection. Proven experience supporting global clinical trials across the U.S., EU, and Asia-Pacific. Strong understanding of oncology trials; experience in cell and gene therapy with CAR-T strongly preferred. Demonstrated experience collaborating with CROs and managing feasibility outputs. Knowledge of global site networks with CAR-T capabilities (preferred). Education Requirements Bachelor’s degree in Life Sciences or related field. Advanced degree (preferred).